- Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, MO, USA
The medullary reticular formation contains large populations of inadequately described, excitatory interneurons that have been implicated in multiple homeostatic behaviors including breathing, viserosensory processing, vascular tone, and pain. Many hindbrain nuclei show a highly stereotyped pattern of localization across vertebrates suggesting a strong underlying genetic organization. Whether this is true for neurons within the reticular regions of hindbrain is unknown. Hindbrain neurons are derived from distinct developmental progenitor domains each of which expresses distinct patterns of transcription factors (TFs). These neuronal populations have distinct characteristics such as transmitter identity, migration, and connectivity suggesting developmentally expressed TFs might identify unique subpopulations of neurons within the reticular formation. A fate-mapping strategy using perinatal expression of reporter genes within Atoh1, Dbx1, Lmx1b, and Ptf1a transgenic mice coupled with immunohistochemistry (IHC) and in situ hybridization (ISH) were used to address the developmental organization of a large subset of reticular formation glutamatergic neurons. All hindbrain lineages have relatively large populations that extend the entire length of the hindbrain. Importantly, the location of neurons within each lineage was highly constrained. Lmx1b- and Dbx1- derived populations were both present in partially overlapping stripes within the reticular formation extending from dorsal to ventral brain. Within each lineage, distinct patterns of gene expression and organization were localized to specific hindbrain regions. Rostro-caudally sub-populations differ sequentially corresponding to proposed pseudo-rhombomereic boundaries. Dorsal-ventrally, sub-populations correspond to specific migratory positions. Together these data suggests the reticular formation is organized by a highly stereotyped developmental logic.
Introduction
The organization of the hindbrain has been of significant interest for well over 100 years. Johnson proposed it could be functionally divided dorso-ventrally into four discrete regions based on the location of afferent and efferent projections, and that this organization was a shared characteristic of vertebrate lineages (Johnson, 1902). Based on comparative analysis in embryonic vertebrates, this organization was extended by Bergquist and Källěn (1954) and others [see review by Nieuwenhuys (2011)] to divide the neuroaxis rostrocaudally into specific neuromeric regions. The volumes circumscribed by these rostro-caudal and dorso-ventral divisions may represent functional “morphological units” that are the consequence of neural migration within a unit (Nieuwenhuys, 2011).
Recent work describing the molecular development of the hindbrain found that the rostro-caudal boundaries of a subset of these regions, now termed rhombomeres, correlate closely with the expression during early development of highly evolutionarily conserved transcription factors (TFs) involved in patterning of the body plan, homeobox (Hox) genes (Krumlauf et al., 1993). Rhombomeric boundaries, however, have only been clearly described for pontine hindbrain regions (R1–R6) (Manzanares et al., 1999; Voiculescu et al., 2001). The caudal R6 boundary and the boundaries of more caudal rhombomeres within the mouse hindbrain are unclear. Work using chick-quail chimeras suggests the existence of at least four “pseudo-rhombomeres” (pr7–10) within the medulla based on the migration and formation of multiple medullary nuclei (Cambronero and Puelles, 2000; Marin et al., 2008). Currently, no genes have been identified in the early developing mouse embryo whose expression correlates with these boundaries. Similarly, based on patterns of TF expression, the hindbrain can be divided dorso-ventrally into at least 16 domains, consistent, at a first approximation, with the four divisions proposed by Johnson (Johnson, 1902; Sieber et al., 2007; Gray, 2008; Storm et al., 2009).
The extension of these organizational heuristics into the postnatal or adult hindbrain has several major limitations. First, the initial hypotheses were based on the analysis of highly identifiable populations that only represent a subset of hindbrain neurons, such as cranial motor pools or the target zones of sensory input (Altman and Bayer, 1980a,b; Kalia and Fuxe, 1985; Vanderhorst and Ulfhake, 2006). Second, they assume that neurons largely remain within their morphological unit and their formation is strictly a function of cellular migration along a radial glial scaffold. Exceptions, such as the precerebellar pontine nucleus and inferior olive, were found to be derived from discrete developmental domains at or near the dorsal surface, the rhombic lip, which then underwent radial migration to positions on the ventral surface (Dymecki and Tomasiewicz, 1998; Nichols and Bruce, 2006; Yamada et al., 2007; Rose et al., 2009b; Storm et al., 2009).
The extent to which other populations of hindbrain neurons, especially within the medulla, share a similar organizational logic has only recently started to be addressed. For example, our understanding of aminergic populations has greatly expanded due to recent analysis of the TFs necessary for their formation (Qian et al., 2001; Cheng et al., 2003; Ding et al., 2003; Zhao et al., 2006). These populations are derived from very specific rostro-caudal and dorso-ventral developmental domains. One major difference was that unlike previously studied populations, several catecholaminergic populations undergo significant migration (Kalia et al., 1985a,b,c). To add to this complexity, a significant number of hindbrain neurons make up the “reticular formation,” i.e., they do not lie within clearly identified nuclei, defined either by neuronal density or gene expression. Brodal, in his seminal description of the reticular formation, defined it as “those areas of the brain stem which are characterized structurally by being made up of diffuse aggregations of cells of different types and sizes, separated by a wealth of fibers travelling in all directions” (Brodal, 1957). Thus, whether the hindbrain has an underlying genetic logic that applies to all neurons is unknown.
A number of large-scale gene expression projects have coupled advances in genomics with anatomy providing a new wealth of information (Gray et al., 2004; Lein et al., 2007; Diez-Roux et al., 2011). This information, however, is limited by our inability to uniquely identify the majority of neuronal populations in the brain. TFs are proteins that directly bind DNA to control the expression of large numbers of genes. While many TFs are either ubiquitious or controlled by activity dependent mechanisms, some are essential for the specification and maintenance of cellular identity (Gray et al., 2004; Gray, 2008). In fact, one very influential idea hypothesizes that the particular combination of TFs expressed during development is the defining characteristic that specifies neural populations (Briscoe et al., 2000; Baumgardt et al., 2007). Because of this, TFs have been extensively used as markers for the identification of specific neural populations. TFs, like all genes, are expressed in multiple cellular populations, but because of their unique function, they provide a unique context for understanding gene expression.
The mouse genome contains ~1500 putative TFs all of which have their own temporal and spatial pattern of expression within the brain (Gray et al., 2004). Of these, only a subset of TFs has been shown to be both spatially limited to and essential for the development of specific subpopulations of neurons. One consequence of the limited number of lineage specific TFs within the mouse genome, compared to the large number of discrete neuronal lineages, is that nearly all TFs are expressed in multiple distinct populations. These populations, however, are often far enough apart within the brain for relatively easy discrimination. In addition, each lineage has unique patterns of TF co-expression. Thus, individually TFs label diverse populations, but within limited regions and/or in combination with other TFs, they define small populations of neurons. These “lineage-specific” TFs are highly useful for the identification of discrete subpopulations of neurons from development into adulthood (Vandunk et al., 2011; Miller et al., 2012). Many TFs, however, are expressed either only transiently or lack high quality commercially available antibodies limiting their use for extensive analysis. One method to overcome these limitations has been to mark specific subsets of neurons by using transgenic mice expressing reporter proteins that either directly, or via Cre-mediated recombinase activity, label cells for extended periods and allow for ease of visualization (Srinivas et al., 2001; Dymecki et al., 2002).
The medullary reticular formation contains a large number of excitatory and inhibitory neurons involved in the control of breathing (Feldman et al., 2013), vasomotor tone (Dampney et al., 1982; Guyenet, 2006; Abbott et al., 2012), pain (Esser et al., 1998; Almeida et al., 2002; Lima and Almeida, 2002), somatomotor functions (Brodal, 1952; Strack et al., 1989; Jansen et al., 1995; Geerling and Loewy, 2008), and a variety of other homeostatic processes. It is also known to have extensive local and distal connectivity. Work from several groups has identified developmental genes important for multiple aspects of these important systems. For example, the TFs Lmx1b (lim homeobox transcription factor 1b) and Phox2b (paired mesoderm homeobox 2b) are fundamental for the formation of multiple brainstem populations including glutamatergic neurons of the nucleus of the solitary tract (NTS) and brainstem catecholaminergic neurons (Yang et al., 1998; Pattyn et al., 1999, 2000a,b; Brunet and Pattyn, 2002; Cheng et al., 2003; Ding et al., 2003; Dubreuil et al., 2009; Ramanantsoa et al., 2011). Phox2b is a homeobox TF also involved in the specification of visceral sensory input and motor output (Brunet and Pattyn, 2002; Dauger et al., 2003). Lmx1b is a homeobox TF also involved in specification of sensory populations as well as serotonergic neurons (Cheng et al., 2003; Ding et al., 2003, 2004; Zhao et al., 2006). Both Phox2b and Lmx1b expression are defining characteristics of several hindbrain lineages. Dbx1 (developing brain homeobox 1) is essential for the formation of glutamatergic preBötzinger Complex (preBötC) respiratory neurons as well subsets of neurons from the spinal cord to the cortex (Pierani et al., 2001; Bouvier et al., 2010; Gray et al., 2010). Ptf1a (pancreas specific transcription factor 1a) is a TF important for the specification of a large percentage of hindbrain and spinal cord inhibitory neurons as well as inferior olive neurons (IO) (Glasgow et al., 2005; Hoshino et al., 2005; Yamada et al., 2007; Brohl et al., 2008). Combined with Lbx1 (ladybird homeobox 1), Ptf1a is vital for the formation of Bötzinger Complex (BötC) glycinergic respiratory neurons (Pagliardini et al., 2008). Similarly, FoxP2 (forkhead box P2) is a leucine zipper transcription factor implicated in motor control in humans (Lai et al., 2001). Previous analyses found FoxP2 is expressed in small subsets of spinal cord, medullary, and pontine neurons in lineage specific manner (Gray, 2008; Prasad et al., 2008; Geerling et al., 2011; Miller et al., 2012). Dbx1 is a homeobox TF necessary for the formation of the preBötC (Pierani et al., 2001; Bouvier et al., 2010; Gray et al., 2010). Neurons derived from lineages expressing these various TFs, however, are broadly localized throughout the hindbrain.
During early neurogenesis (~E9–E11 in mouse), the hindbrain neural progenitor zone can be divided into at least 16 dorso-ventral domains based on discrete patterns of TF expression (Figure 1A) (Sieber et al., 2007; Gray, 2008; Storm et al., 2009). Work from a number of laboratories has shown that each hindbrain and spinal cord progenitor domain has the capacity to produce multiple neural subtypes with distinct migratory paths, neurotransmitter phenotypes, and axonal projection patterns (Helms and Johnson, 2003; Glasgow et al., 2005). At present, the final location and function of the vast majority of these neurons are unknown. A number of recent papers in both mice and rats have described the localization of some of the neurons derived from or expressing specific TFs within the hindbrain, including Atoh1 (atonal homolog 1), Dbx1, Ptf1a, Lmx1b, and Phox2b populations (Qian et al., 2001; Lumpkin et al., 2003; Wang et al., 2005; Kang et al., 2007; Yamada et al., 2007; Pagliardini et al., 2008; Rose et al., 2009a,b; Bouvier et al., 2010; Gray et al., 2010). While informative, it has been difficult to integrate these diverse results into a more general understanding of the hindbrain, especially the medulla.
Figure 1. Genetic diversity of hindbrain neurons. (A) Schematized diagram describing brainstem progenitor domains for eight dorsal (dA1–dB4) and 8 ventral progenitor populations (v0–v3l) based on their relative dorso-ventral location during neurogenesis (left). Partial list of transcription factors expressed within progenitors (italics) or post-mitotic neurons within each domain (middle). Neurotransmitter identity of neurons derived from each domain (right). (B) Cartoon showing partial migratory path of ventral medulla neurons in embryonic mouse brainstem. Colors correspond to domains in (A). Thick arrows correspond to populations migrating to ventrolateral medulla. (C) Pseudo-color confocal image of FoxP2 (green), Pho×2b (magenta), and βgal (cyan) expression in an E13.5 Lmx1b-βgal mouse showing the origin and migration of hindbrain neurons. Colored bars correspond to boundaries of progenitor domains from (A). (D) Pseudo-color confocal image of FoxP2 (magenta) and YFP (green) expression in E13.5 Ptf1a-Cre; R26 YFP medulla. Region in box is expanded to right showing overlapping (top), FoxP2 (middle), and YFP (bottom) expression. Colored bars correspond to boundaries of progenitor domains from (A). (E) Pseudo-color confocal image of intrinsic GFP (green) and βgal (magenta) expression from E13.5 GAD1-GFP; Dbx1-βgal double transgenic mouse. Region in box is expanded to right showing overlapping (top), βgal (middle), and GFP (bottom) expression. Inverted confocal mosaic image showing localization of lineage derived neurons in hemisections from rostral medulla from P0 Atoh1 (F), Lmx1b (G), Dbx1 (H), and GAD1 (I) transgenic mice. Scale bar = 500 μm.
The availability of transgenic mice with genetically encoded reporter genes driven by TF genomic promoter regions allows for the identification of neuron developmental history. I hypothesized that mapping the location of multiple developmental lineages in relation to each other and to medullary glutamatergic neurons present in both the dorsal and ventrolateral medulla may provide insight into the underlying genetic organization of hindbrain interneurons. Using fate-mapping in six transgenic mouse lines that identify the majority of medullary glutamatergic neurons, combined with immunohistochemistry (IHC) and vesicular glutamate transporter in situ hybridization (ISH), I provide a map of the locations of specific subpopulations of medullary reticular formation neurons. From these data, I propose the medulla has a clearly understandable anatomical logic based on dorso-ventral developmental origin and rostro-caudal segmentation. Within the reticular formation, excitatory neurons from specific lineages are located in discrete stripe-like domains that only partially overlap. These populations vary along the rostro-caudal axis in a pattern similar to proposed pseudo-rhombomeric boundaries. Moreover, these data suggest that the developmental origins of many reticular formation glutamatergic neurons can be predicted from their location and function.
Methods
Mice
We employed Atoh1βgal/+ (Atoh1-βgal) (Ben-Arie et al., 1997), Atoh1-Cre (Chen et al., 2002), Dbx1βgal/+ (Dbx1-βgal) (Pierani et al., 2001), Gad1-GFP transgenic (Chattopadhyaya et al., 2004), Lmx1bβgal/+ (Lmx1b-βgal) (Pressman et al., 2000), Ptf1aCre/+ (Kawaguchi et al., 2002), Rosa26-EYFP (Srinivas et al., 2001), and wild type mice. All mice were bred onto a mixed CD1/C57B6 background. Experiments were done in accordance with the Institute for Laboratory Animal Research Guide for the Care and Use of Laboratory Animals. All experiments were approved by the Animal Studies Committee at Washington University School of Medicine.
Mapping TF Lineages in the Medulla
A selected P0 Atoh1-Cre; Rosa26-stop-yellow fluorescent protein mouse hindbrain (Figure 1F, Atoh1-YFP) (Srinivas et al., 2001; Chen et al., 2002) was sectioned at 20 μm into six sets (100 μm separation between sections) from the midbrain to the cervical spinal cord. 4/6 sets were stained for YFP as well as FoxP2, Phox2b, an antibody that recognizes both tyrosine hydroxylase and tryptophan hydroxylase (TH-TPH), or choline acetyltransferase (ChAT). Two-color confocal mosaic images were acquired at 10X for all sections. Reference sections stained for YFP and ChAT were used to manually outline hindbrain sections, motoneuron pools, large Atoh1-derived populations, and other major regions visible as background. Sections, co-stained for YFP and FoxP2, Phox2b, or TH-TPH, within 100 μm of each reference section, were aligned, and major populations were manually outlined. Outlines were smoothened for clarity. The purpose was to provide a comparative analysis of the relative location of distinct developmental lineages, not provide a detailed count of cell number.
Digital mosaic images from similarly sectioned P0 Lmx1b-βgal and Dbx1-βgal hindbrains from approximately identical rostro-caudal regions based on co-expression of ChAT, Phox2b, or FoxP2 were overlain onto reference images and scaled to match size, prior to outlining neuronal populations to define Lmx1b and Phox2b co-expressing regions as well as Dbx1-derived regions. Hindbrain structures were identified by comparison with multiple rodent atlases and existing literature (Kalia and Fuxe, 1985; Kalia et al., 1985a,b,c; Franklin, 1997; Paxinos, 2001; Vanderhorst and Ulfhake, 2006).
In situ Hybridization
Slides were immersed in 4% paraformaldehyde (PFA), permeabilized with proteinase K, washed in 0.1 M triethanolamine-HCl with 0.25% acetic anhydride, blocked in hybridization buffer at 65°C, then placed into slide mailers containing hybridization buffer with digoxigenin (DIG) labeled antisense RNA at 1 μg/ml overnight at 65°C. Slides were washed in sodium citrate buffers at 62°C, then washed and incubated in alkaline phosphatase conjugated anti-DIG antibody in 10% normal horse serum and incubated in nitro-blue-tetrazolium chloride and 5-Bromo-4-chloro-3-indolyl phosphate until cellular labeling is clear. For combined IHC and ISH, slides were permeabilized with RIPA buffer and stained for mRNA expression prior to immunohistochemical labeling.
Genotyping
Mice were genotyped by PCR using primers specific for βgal (5′-GTTGCAGTGCACGGCAGATACACTTGCTGA, 3′-GCCACTGGTGTGGGCCATAATTCAATTCGC), GFP/YFP (5′-GCACGACTTCTTCAAGTCCGCCATGCC, 3′-GCGGATCTTGAAGTTCACCTTGATGCC), Cre recombinase (5′-GCATTACCGGTCGATGCAACGAGTGATGAG, 3′-GAGTGAACGAACCTGGTCGAAATCAGTGCG), Atoh1 (Ben-Arie et al., 1997), Dbx1 (Pierani et al., 2001) and Lmx1b (Pressman et al., 2000) as described, or by direct visualization of fluorescent reporter or βgal reaction product.
Tissue Acquisition
Neonatal pups (P0–P4) or embryos from timed pregnant females (morning of plug = E0.5) were anesthetized and either perfused (≥E16.5) or immersion fixed in PFA in 0.1 M phosphate buffered saline (PBS), pH 7.4. Embryos or isolated brainstems were postfixed in PFA overnight at 4°C, cryoprotected in 25% sucrose in PBS, blocked, frozen in embedding medium, and stored at −75°C. Perinatal mice were used for several reasons; the vast majority of medullary neurons have reached their adult location making comparison with adult tissue simple, the expression of reporter genes is maximized, and many essential medullary functions, such as breathing, are already active. Brainstems were sectioned in sets of six on a Hacker (Winnsboro, SC) cryostat at 20 μm and sections were thaw mounted onto Superfrost Plus slides and stored at −20°C until use.
In situ Hybridization Probes
A 717 base pair cDNA fragment of the mouse VGlut2 gene (bps 1268- 2004, NM_080853) was cloned into a PCRII vector (Invitrogen) from mouse cDNA (Cheng et al., 2004). DIG labeled anti-sense VGlut2 cRNA probes were generated using PCR products as template and T7 RNA polymerase (Roche, Ambion) as previously described (Gray et al., 2010). cRNA probes were purified using Quick Spin columns (Roche) and quantified by spectrophotometry. Probes were used at a concentration of 1 μg/ml. Experiments using sense cRNA probes showed no specific localization.
IHC and ISH Image Acquisition
Fluorescent and brightfield images were acquired using a Nikon 90i microscope (Nikon Instruments, Melville, NY), Roper H2 cooled CCD camera (Photometrics, Tucson, AZ), and Optigrid Structured Illumination Confocal with a Prior (Rockland, MA) motorized translation stage. Pseudo-colored images were acquired in Volocity (Perkin Elmer, Waltham, MA), and modified in Photoshop (Adobe, San Jose, CA) or ImageJ (National Institutes of Health, Bethesda, MD) and exported as 8 bit JPEG images. Images were filtered and levels were modified for clarity.
Antibodies
Chicken anti-beta galactosidase (βgal) 1:4000 (Abcam, Cambridge, MA), Rabbit anti-βgal 1:1000 (Covance, Princeton, NJ), Goat anti-FoxP2 1:2000 (Abcam), Chicken anti-green fluorescent protein (GFP) 1:1000 (Aves Labs, Tilgard, OR), Rabbit anti-GFP 1:2000 (Invitrogen, Carlsbad, CA), Goat anti-Lhx9 1:1000 (Santa Cruz Biotechnology (SCBT), Santa Cruz, CA), Rabbit anti-neurokinin 1 receptor (NK1R) 1:2000 (Advanced Targeting Systems, San Diego, CA, Millipore, Billerica, MA), Rabbit anti-Pax2 1:250 (Invitrogen), Goat anti-Phox2b 1:500 (SCBT), Rabbit anti-Phox2b 1:20,000 (C. Gordis, École Normale Supérieure, Paris, France), Goat anti-somatostatin (SST) 1:600 (SCBT), Rabbit anti-SST 1:500 (SCBT), Guinea pig anti-SST2aR 1:8000 (Gramsch Labs, Schwabhausen, Germany), Sheep anti-tyrosine hydroxylase/tryptophan hydroxylase 1:1000 (Millipore). Chicken anti-TH 1:200 (Aves Labs). Secondary antibodies were species specific and conjugated with FITC, Alexa 488, DyLight 488, Cy3, C5, or DyLight 649 (Invitrogen or Jackson Immunoresearch, West Grove, PA). No specific staining was seen in the absence of any primary antibody.
Results
Figure 1A is a schematic showing the 16 hypothesized hindbrain progenitor domains divided into eight dorsal (d) and eight ventral (v) domains based on previous work, hypothesized from homologies to spinal cord development, and/or data presented below. The medulla contains 15 of these domains, lacking the dB2 domain (Gaufo et al., 2004; Sieber et al., 2007). Strong evidence for the existence of the dorsal domains has previously been described (Gaufo et al., 2003; Sieber et al., 2007; Gray, 2008; Pagliardini et al., 2008; Rose et al., 2009a; Storm et al., 2009). Within the hindbrain, most ventral domains have not been extensively described and are estimated from published work (Garcia-Campmany et al., 2010; Crone et al., 2012). The neurons of the spinal trigeminal nucleus (SpV) are derived from later born subsets of interneurons similar to what is seen in dorsal spinal cord (Figure 1B) (Glasgow et al., 2005; John et al., 2005; Sieber et al., 2007). Each domain expresses a unique combinatorial pattern of TF expression. For each domain, I have listed a subset of TFs expressed either in progenitor cells (italics) or within post-mitotic neurons (Figure 1A, middle). Additionally, each domain produces neurons with defined neurotransmitter expression although this is the first systematic analysis for many of these populations (Cheng et al., 2004; Glasgow et al., 2005). For example, neurons derived from the dA3 domain are glutamatergic and express the TFs Lmx1b and Phox2b (Figure 1A, right) (Qian et al., 2001).
In the E12.5 mouse much of hindbrain neurogenesis is complete, however, domains are relatively easy to visualize as both progenitor and newly born postmitotic neurons are present adjacent to the ventricular zone. Figure 1B shows a cartoon of the location of the dA1-v0 progenitor domains and the migration path of subsets of their neural derivatives (color coded as in Figure 1A). Gray box (Figure 1B) and arrows (Figures 1C–E) indicate mixed Ptf1a- and Lmx1b- derived domains that will form the SpV. Figures 1C–E show the use of combinations of TFs to identify discrete developmental domains. The approximate dorso-ventral lineage boundaries (dA1-v0) are indicated in relation to the location of neurons derived from Lmx1b (Figure 1C), Ptf1a (Figure 1D), or Dbx1-derived lineages (Figure 1E), or expressing FoxP2 (Figures 1C,D) or Phox2b (Figure 1C) proteins. The specific localization of GABAergic neurons is also indicated (Figure 1E). These data point out both the initial strict developmental organization of the hindbrain, but as well as the extensive migration of at least some medullary populations.
The initial laminar development of the hindbrain suggests the majority of interneurons within the hindbrain might remain limited to highly circumspect regions and that neurons derived from different progenitor domains might have little overlap (Figures 1B–E). This has been seen in both xenopus and zebrafish hindbrain (Nikundiwe and Nieuwenhuys, 1983; Ruiz i Altaba and Jessell, 1991; Kinkhabwala et al., 2011; Koyama et al., 2011), but the extent to which this is true in mammals is unclear. To address this, I analyzed the localization of neurons within the perinatal medulla derived from 5 developmental domains: Atoh1 expressing dA1 (Figure 1F), Lmx1b expressing dA3 dB3 and v3l, and Dbx1 expressing v0 (Figure 1H) interneurons (Figure 1G). Together these data include the locations of neurons from 8 of the 15 medullary progenitor domains: dA1, dA3–dA4, dB3, v0v-c, and v3l and include a large percentage of medullary glutamatergic neurons as well as all aminergic and subsets of cholinergic (see below) and GABAergic neurons (Helms and Johnson, 1998; Pressman et al., 2000; Moran-Rivard et al., 2001; Pierani et al., 2001; Cheng et al., 2004; Gray, 2008; Miesegaes et al., 2009; Rose et al., 2009a). As expected for linage-specific TFs, each gene labeled neurons in discrete locations consistent with previous work. For comparison I also analyzed the localization of a subset of GABAergic neurons in glutamic acid decarboxylase 1-green fluorescent protein (GAD1-GFP) transgenic mice (Figure 1I) (Chattopadhyaya et al., 2004). GABAergic neurons are present throughout most of the medulla.
Figures 1F–I show the localization of gene reporters yellow fluorescent protein (YFP), β-galactosidase (βgal), and GFP for four mouse lines (Atoh1-Cre, Lmx1b-βgal, Dbx1-βgal, and GAD1-GFP) in P0 hindbrain at the level of the rostral medulla. In agreement with the highly controlled expression of TFs, the localization of reporter gene expressing cells was consistent in multiple mice indicating that fate-mapping is an efficient way to identify developmentally defined subsets of hindbrain neurons. Importantly, neither Atoh1 nor Dbx1 proteins are expressed in post-mitotic neurons. Similarly, GAD1 protein is largely limited to synaptic terminals. Hence, a fate-mapping approach is the only way to clearly identify these populations. Given their distinct developmental lineages, fate-mapped populations show unique and largely non-overlapping patterns of localization that only partially overlap with GAD1 expressing regions. For example, Atoh1-derived neurons clearly label the external cuneate and linear nuclei (Li, Figure 1F), while Lmx1b-derived neurons are present within the NTS and raphe nuclei (Figure 1G). Thus, the localization of significant numbers of medulla neurons is consistent with a limited migration from the progenitor zone. In contrast, all four lineages are also expressed in the ventrolateral medulla and within adjacent intermediate reticular regions. Hence each lineage appears to maintain stereotyped subpopulations with limited dorso-ventral mixing. Some regions, such as the ventrolateral medulla and regions of the reticular formation show possibly overlapping populations. This raises questions as to what extent and where do distinct developmental subpopulations intermingle within the medulla? Answering this might be an important step to define regions of specific lineage for the future understanding of connectivity and gene expression. To address this, I set out to map the regions of expression for each multiple TF lineages onto a single reference brain set.
Mapping TF Lineages in the Medulla
Figure 2A is a sagittal line drawing of the adult mouse hindbrain modified from Paxino's atlas of the adult mouse brain at the level of the lateral reticular nucleus (LRN) (Franklin, 1997). The approximate boundaries of rhombomeres 6 and 7 are indicated. The caudal boundary of rhombomere 5 is based on the caudal extent of labeling in EGR2 (early growth factor 2, aka Krox20) transgenic mouse lines (Voiculescu et al., 2001; Manzanares et al., 2002). The rostral boundary of rhombomere 7 is based on the rostral extent of HoxA4 expression while the caudal boundary is an estimate based on size (Rivkin and Cordes, 2008; Huang et al., 2012). Figures 2B–J outlines the regions where distinct developmentally defined cells are located within the neonatal medulla at approximately 100 μm rostro-caudal resolution. Identified regions are indicated (see abbreviations). Atoh1-, Dbx1-, and Lmx1b- derived populations are present along the entire length of the medulla. For example, the dA3 Lmx1b/Phox2b population that specifies NTS and medullary catecholaminergic neurons has no direct homolog in the cervical spinal cord and ends near the hindbrain/spinal boundary (Figure 2J). Atoh1- and Dbx1- derived populations both continue to the sacral spinal cord (not shown). In general, the localization of developmentally defined populations are clearly not organized within a strictly nuclear organization as within the thalamus, nor are the populations largely intermingled as is seen in spinal cord (Helms and Johnson, 2003; Gray et al., 2004; Garcia-Campmany et al., 2010).
Figure 2. Atlas of reticular formation developmental origin in neonate mouse medulla. (A) Mid-sagittal cartoon showing approximate region of mapping (red dashed box). Boxes below hindbrain indicate rhombomere 6 and 7 boundaries. Blue lines indicate pseudo-rhombomere 7–10 boundaries. Italicized letters indicate rostro-caudal position of sections in map. Image modified from Franklin (1997). (B–J) Outlines of medullary sections from rostral (B) to caudal (J) are shown. Sections are separated by 100 μm. Colored lines indicate regions where cells expressing or derived from specific TF lineage are present in P0 mouse (see legend). Red indicates regions of Lmx1b and Phox2b co-expression. Location of motoneurons and monoaminergic populations are included for reference. Scale bar = 500 μm. See abbreviations for explanation of text.
The medulla contains many populations identifiable using Nissl staining (Altman and Bayer, 1980a,b; Kalia and Fuxe, 1985; Vanderhorst and Ulfhake, 2006). Most of these also correspond to populations where a single lineage is predominant. Several of these populations are located adjacent to their progenitor domains, (Figures 1B,C) consistent with limited migration, and show limited population mixing. For example, Atoh1-derived, dA1 neurons of the vestibular, gracilis, and cuneate nuclei lie dorsal to the subset of dA3 Lmx1b- and Phox2b-derived neurons that form the NTS (Figures 2C–H). Note that by P0, not all Lmx1b-derived NTS neurons continue to express Phox2b likely due to down regulation of Phox2b protein as is seen in other populations (Figure 3C) (Pattyn et al., 1997; Dubreuil et al., 2000). Other populations with known patterns of migration such as the dA1, Atoh1-derived pre-cerebellar glutamatergic neurons of the LRN (Figures 2E–J) and their continuation the Li (Figures 2C,D) (Rose et al., 2009a), as well as the dA4, FoxP2 expressing IO are also clearly defined (Yamada et al., 2007; Storm et al., 2009). In addition, portions of the prepositus hypoglossi and nucleus of Roller (Pr, nRO, Figures 2B,D) are also dA1, Atoh1-derived populations as previously described (Fu et al., 2009; Rose et al., 2009a; Ray et al., 2011). The nRO and Pr lie near the midline and projects to cerebellum similar to the Atoh1-derived, pre-cerebellar neurons in the spinal cord (Brodal, 1952; Miesegaes et al., 2009).
Figure 3. Segmental organization of combinatorial patterns of gene expression within rostral medulla hindbrain lineages. Pseudo-color fluorescent confocal mosaic hemi-sections from P0 transgenic mice at the level of pseudo-rhombomere 7 (A–F) and 8 (G–L). Images from Lmx1b-βgal (A–C,G–I), Dbx1-βgal (D,E,J,K), and Atoh1-Cre; R26YFP (F,L) mice showing localization of lineage reporter (green) β-Gal (A–E,G–K) or YFP (F,L) with reference genes (magenta) TH (A,G) FoxP2 (B,F,H,K,L) Phox2b (C,I) Pax2 (D), SST2aR (E), or SST (J). Boxed region in each image is expanded to right showing overlapping (top), and single colors magenta (middle), and green (bottom). Arrows indicate co-expression. Arrowheads indicate absence of co-expression. See Figures 2C,E for identification of specific regions. Scale bar = 500 μm.
Defining the Reticular Formation
Outside of the clearly identifiable medullary regions, i.e., within the reticular formation, the localization of developmentally defined populations remained highly stereotyped. In addition to the NTS, Lmx1b, and Phox2b are co-expressed in both dorsal and ventral TH expressing neurons (Figures 2, 3A,G, 4A,G, 6C,G), as previously described (Pattyn et al., 1997, 2000a; Qian et al., 2002). Lmx1b and Phox2b also define the non-TH expressing intermediate reticular formation (IRt) at rostral medullary levels (Figures 2C,I). These neurons have been shown to express Phox2b in the adult rat, but their co-expression with Lmx1b suggests they are developmentally related to the NTS and may be involved in secondary viscerosensory processing (Kang et al., 2007).
The reticular zone just medial to the spinal nucleus of the trigeminal nerve (SpV) has been shown to be important for the coordination of pain and eye blink reflex pathways (Almeida and Lima, 1997; Almeida et al., 1999; Lima and Almeida, 2002; Leite-Almeida et al., 2006; Smit et al., 2006), and receives direct cortical and spinal input (Desbois et al., 1999). Lmx1b-derived neurons were present within the parvocellular reticular formation and dorsal medullary reticular nucleus (PCRt, MdD, Figures 2B–H). Neither of these populations co-expressed Phox2b (Figures 3I, 4C). This suggests these populations may be derived from later born Lmx1b-derived neurons that migrate to the SpV and may correspond developmentally and possibly functionally to late-born, deep dorsal horn neurons in the spinal cord (Ding et al., 2004; Glasgow et al., 2005).
The distribution of v0, Dbx1-derived neurons is less localized to discrete regions, but still shows a clear spatial organization. A subpopulation within the rostral medulla is located lateral to their developmental origin (Figures 2B,C). It lies ventral to the vestibular nuclei and medial to the NTS and largely overlapping to the Pr (Figures 3E,F) with scattered neurons extending ventrally. This suggests Dbx1-derived neurons make up a significant part of the Pr nuclei although whether these are glutamatergic or GABAergic is unknown (McCrea et al., 1979). In the spinal cord, the majority of Dbx1-derived neurons migrate ventro-medially toward the midline (Pierani et al., 2001; Lanuza et al., 2004). A similar population is present within the mid to caudal medulla extending into the spinal cord (Figures 2C–J). In the spinal cord, these largely GABAergic neurons have been proposed to play a role in coordinating alternating activity during locomotion (Lanuza et al., 2004).
Dbx1-derived neurons are also present within a narrow stripe extending from the dorsomedial to ventrolateral surfaces of the medulla. Within the medial medulla, this population is clearly separate from the medially migrating population described above (Figures 2C–F, 3D,E,J,K). Within the intermediate reticular formation (IRt), Dbx1-derived neurons form a narrow stripe that partially overlaps with Lmx1b/Phox2b neurons (Figures 2B–D) but does not overlap with the dorsal medullary reticular nucleus (MdD) neurons (Figures 2E–H). Within the caudal medulla (Figures 2G–J, 4E,L), the stripe of Dbx1-derived neurons is less apparent due to both the size of the population and the more compact area of the medulla.
The ventrolateral medulla contains neurons from multiple progenitor domains including catecholaminergic dA3, Lmx1b/Phox2b- derived neurons, small populations of undescribed FoxP2 neurons, and dA1, Atoh1-derived neurons. It also contains an expansion, relative to the spinal cord, of the v0v, Dbx1-derived stripe forming the neurons of the respiratory column (Gray et al., 2010). This developmental variety is consistent with previous results regarding the heterogeneity of ventral respiratory and cardiovascular control regions and will be discussed in more detail below.
Figure 2 also includes the localization of FoxP2. FoxP2 is co-expressed by several different lineages. However, this protein and its expression are highly conserved in rats and mice and persist in adult rat brain (Alvarez et al., 2005; Stein and Loewy, 2010; Geerling et al., 2011; Miller et al., 2011, 2012; Shin et al., 2011). FoxP2 was previously found expressed in subsets of Atoh1- and Lmx1b-derived pontine neurons as well as several subpopulations of spinal cord neurons (Alvarez et al., 2005; Prasad et al., 2008; Geerling et al., 2011; Miller et al., 2012). The availability of high-quality, commercially available antibodies makes it a good marker for defining specific hindbrain populations. FoxP2 is expressed within the Ptf1a-derived, dA4 population that forms the IO in nearly every neuron (Figures 2D–J, 3H, 4E,I). It is also expressed within a subset of vestibular nuclei neurons (Figure 3B) and throughout the medulla in small, scattered populations (Figures 3H, 4B,H). As FoxP2 was expressed along the entire length of the medulla, its co-localization was analyzed in Atoh1-, Dbx1-, and Lmx1b-derived populations. FoxP2 was not co-expressed with Phox2b within the medulla. FoxP2 was also not expressed in medullary dA1, Atoh1-derived neurons (Figures 3F,L, 4F,K) except for a small number of the caudal most IO neurons. This latter co-expression may represent leakage of Atoh1-driven recombinase expression into the most caudally derived IO neurons (Chen and Keens, 2004; Tsuda et al., 2005). FoxP2 was co-expressed in a small subset of Lmx1b-derived neurons in the ventral medulla (Figures 3B,H, 4B,H) from the rostral medulla to the spinal cord border with the population becoming more apparent at caudal levels. Based on their location relative to other Lmx1b populations, these neurons likely represent a subset of dB3 interneurons. FoxP2 was not expressed in Dbx1-derived neurons within the ventral medulla, but was co-expressed in a subset of neurons ventrolateral to the XII motor nucleus (Figure 4E) similar to spinal cord (Prasad et al., 2008).
Figure 4. Segmental organization of combinatorial patterns of gene expression within caudal medullary hindbrain lineages. Pseudo-color fluorescent confocal mosaic hemi-sections from P0 transgenic mice at the level of pseudo-rhombomere 9 (A–F) and 10 (G–L). Images from Lmx1b-βgal (A–C,G,H,J), Ptf1a-Cre; R26YFP (D, I) Dbx1-βgal (E,L), and Atoh1-Cre; R26YFP (F,K) mice showing localization of lineage reporter (green) βGal (A–C,E,G,H,J,L), or YFP (D,F,I,K) with reference genes (magenta) TH (A,G), FoxP2 (B,D–F,H,I,K), Phox2b (C,J), or Pax2 (L). Arrows indicate co-expression. Boxed regions are expanded to right showing overlapping (top), and single colors magenta (middle), and green (bottom). Scale bar = 500 μm.
Combinatorial Coding and the Pseudo-Rhombomeric Model
These data are consistent with the hypothesis that the organization of the medullary reticular formation is a direct consequence of developmental lineage. Previous work has shown much of pontine organization is the direct result of early segmental-like patterning (Krumlauf et al., 1993). Puelles and colleagues, working in chick, proposed the medulla is similarly patterned and consists of multiple pseudo-rhomobomeres with specific neuronal populations being derived from specific rostro-caudal regions of the early neuroepithilum (Cambronero and Puelles, 2000; Marin et al., 2008). Based on homology with chicken hindbrain, Figure 2A includes the approximate pseudo-rhombomeric boundaries. Whether this organization is present within mouse hindbrain is unclear.
As yet, no TFs have been identified in the mouse with rostral or caudal boundaries that correspond to the proposed pseudo-rhombomeric boundaries similar to Hox genes. In the chick the LRN and IO are proposed to be derived from pseudo-rhombomere 9 (pr9) progenitors. In the mouse, both Li and the LRN are Atoh1-derived and have been proposed to be continuous with Li neurons sitting dorsal to the nucleus ambiguous (NA) and LRN on the ventral surface (Fu et al., 2009). Li neurons, however, are limited to the approximate region of pr7 along with the compact formation of the NA (cNA) with a diffuse transition until it forms the LRN in pr9 (Figures 3F,L, 4F,K). Thus, at some basic level, there is extensive anatomical conservation within the medulla between species at least within highly recognizable structures. If this hypothesis is accurate, however, it should be possible to find distinct differences in gene expression between developmentally related neurons over short rostro-caudal distances.
To address whether pseudo-rhombomeric organization might provide a useful way to analyze the organization of the medulla, the combinatorial expression of TF lineage was analyzed to determine whether discrete subpopulations might be genetically identifiable. Figures 3, 4 show confocal mosaic hemisections of Lmx1b, Ptf1a, Dbx1, and Atoh1 transgenic reporter mice co-stained with various antibodies for comparison. Sections correspond to approximate pseudo-rhombomeric boundaries (pr7; Figures 3A–F, pr8; Figures 3G–L, pr9; Figures 4A–F, pr10; Figures 4G–L). In contrast to this hypothesis, several populations were found whose locations were either continuous across the hindbrain or were more consistent with existing rhombomeric populations. Atoh1-derived neurons consist of at least two distinct subpopulations. First are pre-cerebellar neurons such as the LRN that express the TF BarH-like 1 (BarHL1) and express vesicular glutamate transporter 1 (VGlut1) (Bermingham et al., 2001; Gray et al., 2004). Second are small populations of interneurons that express the related TFs Lhx9 and Lhx2 (lim homeobox 2, 9) and vesicular glutamate transporter 2 (VGlut2). In the ventral medulla, the VGlut2 and Lhx9 expressing subset of interneurons are ventral to Dbx1- and Lmx1b-derived populations and are in addition to the Atoh1-derived Li and LRN neurons (Figure 6C) (Helms and Johnson, 2003; Gray et al., 2010; Machold et al., 2011). In the pr7 region, these dA1 neurons are scattered surrounding the rostroventrolateral medulla (RVLM) region (Figure 5D). In pr8–9 they are located ventral to Dbx1-derived and Lmx1b-derived glutamatergic neurons, overlying the LRN (Figures 6C,F-G, 7I) (Gray et al., 2010). Similarly, a subset of Dbx1-derived cells expresses Pax2 across the entire ventral medulla (Figures 3D, 4L). In neither case is there any obvious segmental organization. The Lmx1b/Phox2b neurons of the IRt extend to the approximate rostral rhomobomere 7 boundary (Figures 2B–D, 3C), and Lmx1b/FoxP2 expressing neurons extend the approximate length of rhombomere 7 (Figures 2F–H, 4B,H).
Figure 5. Pseudo-rhombomere 7 specific patterns of gene expression. Pseudo-color fluorescent confocal mosaic images from P0 transgenic mouse at the level of pseudo-rhombomere 7. (A) Schematic image modified from Figure 2C indicating location of co-expressing populations shown in (B–I). (B–I) Images from Dbxl-βgal (B,G,H), Lmx1b-βgal (C), Atoh1-Cre; R26YFP (D–F) and Ptf1a-Cre; R26YFP (I) mice showing localization of lineage reporter β-gal (B,C, magenta, G,H, blue), or YFP (D–F, green) with ChAT (B,C, green), Lhx9 (D, magenta), NK1R (E, magenta, H, red), SST2aR (F,I, magenta, G, red), and Phox2b (G,H, green). Boxed regions in (B–F,I) are expanded to right showing overlapping (right, top), and single colors magenta (middle), and green (bottom). Boxed regions in (G,H) are expanded (inset) with single colors red (right, top), green (middle), and blue (bottom). Scale bar = 500 μm.
Figure 6. Pseudo-rhombomere 8 specific patterns of gene expression. Pseudo-color fluorescent confocal mosaic images from P0 transgenic mouse at the level of pseudo-rhombomere 8. (A) Schematic image modified from Figure 2E indicating location of co-expressing populations shown in (B–H). (B–H) Images from Lmx1b-βgal (B), Atoh1-Cre; Rosa26YFP (C,F,G), Dbx1-βgal (D,E),and wild type (H) mice showing localization of lineage reporter (green) βgal (B,D, green, E, blue), or YFP (C,F,G) with TH (B), SST2aR (C,E,H), NK1R (E,H), Phox2b (E), and Lhx9 (F,H). Text color indicates gene color in images. Boxed region in (B–D,F–H) is expanded to right showing overlapping (right, top), and single colors magenta (middle), and green (bottom). Boxed region in (E) is expanded (top) with single colors red (right, top), green (middle), and blue (bottom). Scale bar = 500 μm.
Figure 7. Pseudo-rhombomere 9 specific patterns of gene expression. Pseudo-color fluorescent confocal mosaic images from P0 transgenic mouse at the level of pseudo-rhombomere 9. (A) Schematic image modified from Figure 2G indicating location of co-expressing populations shown in (B–I). (B–I) Images from Dbx1-βgal (B,D,E), Lmx1b-βgal (C), wild type (F), and Atoh1-Cre; R26YFP (G–I) mice showing localization of lineage reporter (green) β-gal (B–E) or YFP (G–I) with SST2aR (B,C,H), NK1R (D,E,G), or Lhx9 (I). Text color indicates gene color in images. Boxed region in (B–E,G–I) is expanded to right showing overlapping (right, top), and single colors magenta (middle), and green (bottom). Boxed region in (E) is expanded (bottom left) with single colors red (right, top), green (middle), and blue (bottom). Scale bar = 500 μm.
Alternately, it is possible that segmental organization may not appear as the generation of novel hindbrain populations, but is present as differences in gene expression within developmentally related populations. Because of the importance of populations within the ventrolateral medulla in homeostatic control, the expression patterns of multiple genes have been analyzed in some detail providing an additional test. I analyzed the expression of ChAT, somatostatin peptide (SST), SST2a receptor (SST2aR), and neurokinin 1 receptor (NK1R) across the medulla (Pilowsky, 2008; Pilowsky et al., 2009). The hindbrain contains a number of distinct populations of cholinergic interneurons, most notably within the rostral pons (Vanderhorst and Ulfhake, 2006). At least two distinct subpopulations of ChAT expressing interneurons are present within the rostral medulla exclusively within the pr7 region (Figure 5A). One population is Dbx1-derived and is dorsal to the cNA (Figure 5B). A second population is Lmx1b-derived and lies within the pr7 region (Figure 5C). This region overlaps the RVLM region important for control of vasomotor tone (Chalmers et al., 1992, 1994; Guyenet, 2006; Stornetta et al., 2012). This population does not express FoxP2 or Phox2b.
Strong cell-body IHC expression of SST peptide is limited to a subset of Dbx1-derived, preBötC interneurons (Figure 3J) (Stornetta et al., 2003; Llona et al., 2004; Llona and Eugenin, 2005; Bouvier et al., 2010; Gray et al., 2010). While the preBötC abuts the approximate rostral boundary of rhombomere 7 (Figures 2A,E, 6A), its caudal boundary is more consistent with the pr8/pr9 than rhombomere 7/8 boundary (Figure 7A). SST2aR is expressed on distinct subsets of neurons throughout the ventral medulla as well as other regions (Schindler et al., 1997; Burke et al., 2008; Gray et al., 2010). Lmx1b-derived TH neurons co-express SST2aR across the ventral medulla with no clear boundary (Figure 7C) (Burke et al., 2011). Within Dbx1-derived neurons, SST2aR expression is more complex. It is not expressed on Dbx1 neurons in pr7, but is expressed on Dbx1 neurons within the preBötC (pr8, Figure 6E) as well as within the rVRG (pr9, Figure 7B). Within the preBötC, SST2aR is co-expressed with SST peptide indicating a possible auto-regulatory role (Gray et al., 2010).
Lhx9 expressing neurons dorsal to the LRN (pr9) express SST2aR (Figures 7F,H) but more rostral (pr7–8) neurons do not (Figures 5F, 6H). Within pr7, r Dbx1-derived V0 neurons do not express SST2aR (Figure 5G). Lmx1b- and Phox2b-derived, TH expressing dA3 neurons, however, do express SST2aR, but they represent only a subset of SST2aR neurons (Figure 5G). Recently, a population of non-catecholaminergic, glutamatergic neurons that express high levels of SST2aR within the RVLM of the rat was identified (Burke et al., 2008). Based on anatomy and pharmacology, it was proposed these neurons are fundamental for the generation of the basal vasomotor tone, but their relationship to other brainstem SST2aR expressing populations was unknown. An identical population is present in the mouse RVLM (Figure 5I). This population of SST2aR expressing neurons is derived from Ptf1a expressing progenitors and is completely limited to the RVLM/ventral pr7 region (Figures 5F,G,I). This is surprising as Ptf1a-derived neurons are almost exclusively inhibitory within the medulla except for FoxP2 expressing glutamatergic, IO within pr9–10 (Figures 4D,I). These data suggest that the functionally identified region represent a previously unidentified developmental population consistent with a specific functional role.
This pattern of limiting peptide receptor expression to subsets of neurons within specific rostro-caudal population is not ubiquitous. NK1R is expressed on Dbx1-derived neurons throughout the ventral medulla, although its expression is highest within the preBötC (Figures 5H, 6D, 7D,E) (Gray et al., 1999, 2010; Guyenet et al., 2002). Similarly, NK1R is expressed on a subset of Lhx9 expressing, Atoh1-derived neurons across multiple pseudo-rhombomeres (Figures 5E, 7G) (Rose et al., 2009b; Gray et al., 2010). Thus, while NK1R expression is not regionally restricted, it is clearly co-localized with other genes in a region specific manner.
Transmitter Identity
One major component of neural identity, neurotransmitter, is a direct consequence of developmental program. The expression of neurotransmitter generating enzymes such as glutamic acid decarboxylases (GAD1-2), or transmitter specific transporters such as the vesicular glutamate transporters (VGlut1-3, Slc17A6-8) begins co-incident with the specification of neural identity (Cheng et al., 2004). In the hindbrain, all three VGlut proteins are present, however, VGlut1 is largely limited to the subset of Atoh1-derived pre-cerebellar subpopulations such as the LRN, and VGlut3 is expressed in a subset of caudal raphe neurons (Hisano et al., 2002; Stornetta et al., 2002a,b; Boulland et al., 2004; Fremeau et al., 2004; Stornetta et al., 2005). Hence, VGlut2 (Slc17A6) is the major enzyme coordinating a glutamatergic phenotype in the hindbrain. The data presented suggest neurons derived from different developmental lineages migrate into specific anatomical regions. This raised the question whether TF lineage could identify distinct glutamatergic populations.
Figures 8A–C shows (ISH) for VGlut2 at three levels of the medulla corresponding to pseudo-rhombomeres 7–9 (Figures 8D, 9A,G). Schematic outlines indicate the relative positions of neurons derived from Dbx1, FoxP2, Lmx1b, and/or Phox2b lineages. Chx10 (ceh-10 homeodomain containing homolog 10) is a defining TF for the v2a population and has recently been shown to be essential for a large medial VGlut2 expressing population (estimated in Figures 8B,C) (Crone et al., 2012). As indicated in Figure 1, these TFs are expressed in subsets of glutamatergic neurons, but also in other populations including GABAergic, catecholaminergic, cholinergic, and serotonergic neurons. To more directly test whether glutamatergic populations correspond to specific developmental lineages, combined ISH for VGlut2 and IHC for reporter genes was performed in the medulla.
Figure 8. Developmental origin of medullary reticular formation glutamatergic neurons. Brightfield in situ hybridization of VGlut2 mRNA from P0 mouse brain overlain with modified outlines from brain outlines from Figures 2C (A, pr7), 2E (B, pr8), and 2G (C, pr9). Colored boxes indicate populations derived from distinct developmental lineages (see legend). (D) Schematic image modified from Figure 2C indicating location of glutamatergic populations of pr7 shown in (E–I). (E–I) Images showing inverted VGlut2 mRNA (magenta) and βgal (green) from Dbx1-βgal (E,G), and Lmx1b-βgal (F,H,I). Single color images shown to right. VGlut2 (top, brightfield), β-Gal (bottom). Arrows indicate co-expression. Arrowheads indicate absence of co-expression. Scale bar = 500 μm.
Figure 9. Developmental origin of medullary reticular formation glutamatergic neurons. Schematic image modified from Figure 2E (A) or from Figure 2G (G) indicating location of glutamatergic populations of pr8 (B-F) or pr9 (H-K). (B-F, G-K) Images showing inverted VGlut2 mRNA (magenta), βgal (green), and FoxP2 (J1, green) from Dbx1-βgal (B, C, H, I), Lmx1b-βgal (D-F, J2-K) and wild type (J1) mice. Note (J1) and (J2) are from the same region from different animals. Single color images shown to right. VGlut2 (top, brightfield), βGal (bottom). Arrows indicate co-expression. Arrowheads indicate absence of co-expression. Scale bar = 500 μm.
Within pr7, the majority of NTS glutamatergic neurons are Lmx1b- and Phox2b- derived (not shown). The lateral MdD, Lmx1-derived population shows a high percentage of Lmx1b derived glutamatergic neurons (Figure 8H). Some of the remaining glutamatergic neurons may be dA1, Atoh1-derived neurons (Figure 1F) (Rose et al., 2009a). Ventral to the NTS, the IRt region has a high density of glutamatergic neurons derived from both Dbx1 and Lmx1b lineages (Figures 8F,G). Within this region, most Lmx1b-derived are glutamatergic. Dbx1-derived neurons consist of a mixture of glutamatergic, GABAergic, and cholinergic neurons as well as glia.
The RVLM contains both Dbx1- and Lmx1b-derived glutamatergic neurons (Figures 8E,I). Most dA3, Lmx1b-, and Phox2b-derived neurons co-express VGlut2 and TH, as in rat (Stornetta et al., 2002b). Nearly 50% of Dbx1-derived cells co-express VGlut2. The majority of non-glutamatergic Dbx1-derived βgal expressing cells, within this region, are glia (Fogarty et al., 2005; Gray et al., 2010).
Within pr8 (Figure 9A), the Lmx1b-derived glutamatergic population lateral to the NTS persists (Figure 9E). Ventral to the NTS, the IRt region contains a continuation of the pr7 dA3, Lmx1b-, and Phox2b-derived population as well as a smaller unlabeled additional population (Figure 9D). These unknown neurons are not Dbx1-derived and they do not express FoxP2. Based on their location, they may be a subset of Ptf1a-derived, dA4 interneurons, although this remains to be shown.
At this level, Dbx1-derived glutamatergic neurons extend from directly lateral to the XIIn to the ventral medullar surface (Figures 9C,H) and show limited overlap with other populations (Figures 9B,C). The dorsal region corresponds with regions of XII pre-motor neurons identified by tracing and calcium imaging studies (Dobbins and Feldman, 1995; Koizumi et al., 2008). The ventrolateral population corresponds to glutamatergic preBötC respiratory neurons. Serotonergic Lmx1b-derived neurons do not express VGlut2 as previously shown (Figure 9F) (Ding et al., 2003).
Figure 9G shows the schematic from Figure 8C and indicates the location of pr9 populations. Similar to pr7 and pr8, Dbx1 glutamatergic neurons are present ventrolateral to dorsomedial (Figures 9H,I) and both the NTS and dorsal population of Lmx1b derived neurons are still present (Figure 9K). Pr9–10 contains a large population of FoxP2 expressing neurons in the ventral reticular formation (Figures 2F–H, 4B,H). These neurons are nearly all glutamatergic (Figure 9J1) and most are Lmx1b derived (Figure 9J2). The Lmx1b/FoxP2 expressing neurons likely represent previously undescribed population of dB3 interneurons.
Discussion
The medulla is a complex structure consisting of multiple heterogeneous populations in close proximity. Outside of populations recognizable by either Nissl stain or by the small number for which genetic markers have been identified, the overall organization of this vital brain region has remained largely unknown. In contrast, during early development, the different classes of neurons are formed in an orderly fashion along the neural tube. I hypothesized that aspects of this early developmental organization persist and form the basis for an orderly pattern of neural organization in the developed medulla.
Focusing on developmental progenitor populations that generate glutamatergic neurons, I used a fate-mapping strategy in multiple transgenic mouse lines coupled with ISH and IHC to identify and map populations of neurons derived from Atoh1, Dbx1, and Lmx1b expressing lineages. Briefly, the major finding is that the medulla is structurally organized in both the dorso-ventral and rostro-caudal axes. Except for some specific exceptions (see below), glutamatergic neurons of the medullary reticular formation are organized into a series of dorso-ventral stripes that correspond to paths of migration from early progenitor domains. These stripes only partially overlap. Within a single developmentally derived stripe, however, there are clear differences in gene expression between ventral and dorsal regions.
Rostro-caudally, similar differences in gene expression within a developmental domain roughly correlate with hypothesized pseudo-rhombomes identified in avian brainstem (Cambronero and Puelles, 2000; Marin et al., 2008). The presence of specific developmentally derived populations, such as the IRt and v0c cholinergic neurons (see below), provides some evidence consistent with this model. Also consistent are the boundaries of peptide receptor expression within Dbx1 neurons of the ventrolateral medulla. The difficulty is that in the absence of clear genetic boundary markers similar to that shown in pons such as Egr2 (Krox20) (Voiculescu et al., 2001; Manzanares et al., 2002), these descriptions remain somewhat anecdotal in mammals. Regardless, however, the pseudo-rhombomeric model allows for a reproducible and understandable way of defining the medulla that should allow for a better estimation of anatomical location for both this work and future studies.
Within the approximate pr7 region (Figures 2B,C) there are multiple previously unknown or under described populations. Just ventral to the NTS, the IRt has previously been described as a Phox2b expressing population in adult rat (Kang et al., 2007). Based on fate-mapping, I show that this glutamatergic population (Figures 8F, 9D) is derived from the dA3, Lmx1b, and Phox2b expressing domain similar to the NTS, although it does not receive direct vagal input from the periphery.
Ventral to IRt and dorsomedial to the cNA is a population of cholinergic interneurons derived from Dbx1 expressing progenitors (Figure 5B) that may be similar to Pitx2 expressing, Dbx1-derived, v0c interneurons that make large C-boutons onto spinal motoneurons. In spinal cord, these neurons are important for the cholinergic modulation of motoneuron function and they make large c-bouton synapses onto lumbar motoneurons (Miles et al., 2007; Zagoraiou et al., 2009; Miles and Sillar, 2011). Unlike the spinal cord, however, these neurons are not located adjacent to the 4th ventricle, the medullary equivalent of the central canal. Previous work suggests Pitx2 is not expressed within the hindbrain (Diez-Roux et al., 2011), but these neurons may be the source of large cholinergic boutons present on cranial motoneurons in pig and mouse brainstem including the XII. These neurons are present in adult rat where a subset has been shown to project to XIIn (Travers et al., 2005).
Ventral to the cNA, in addition to the well-known RVLM catecholaminergic and BötC glycinergic neurons there are several additional populations. First, a small population of cholinergic neurons are present adjacent to lateral portion of the raphe magnus and just caudal to the VIIn (Figure 5C). The functional role of this population is unknown although it has recently been shown to project to brain regions important for sensory, but not autonomic, respiratory, or endocrine regulation (Stornetta et al., 2012). Additionally they may be responsible for fast cholinergic EPSPs found in cNA motoneurons (Zhang et al., 1983) or cholinergic modulation of NTS or respiratory function (Bieger, 2001; Shao and Feldman, 2009). Given their location adjacent to the raphe, this population may be derived from the V3l, Lmx1b domain that also produces serotoninergic neurons (Cheng et al., 2003; Ding et al., 2003; Craven et al., 2004; Pattyn et al., 2004; Alenina et al., 2006; Zhao et al., 2006).
The RVLM has long been known to contain glutamatergic populations modulating vasomotor tone, the most well-known being Lmx1b-derived catecholaminergic neurons (Figure 6B). It was hypothesized some subset of these neurons might be responsible for generating basal tone as ablation of this region blocks neurogenic hypertension (Varner et al., 1994; Pilowsky et al., 2009), although the ablation of spinally projecting catecholaminergic has only limited effect on basal blood pressure (Guyenet et al., 2001; Madden and Sved, 2003). Burke and colleagues identified, in adult rat, a small population of non-catecholaminergic neurons, spinally projecting, SST2aR expressing, glutamatergic neurons and showed that local application of SST into the RVLM caused dose-dependent sympathoinhibition and hypotension (Burke et al., 2008). They proposed these neurons play a role in generating vasomotor tone. Interestingly, the mouse RVLM also contains a possibly equivalent SST2aR expressing population (Figures 5F,G,I). These neurons are a small subpopulation of Ptf1a derived interneurons (possibly dA4, Figure 5I). Nearly all Ptf1a-derived neurons, however, are inhibitory with only the IO known to express VGlut2 (Figures 4D,I) (Yamada et al., 2007). As the IO is derived from more caudal brainstem structures, I propose these SST2aR neurons represent a novel population of glutamatergic Ptf1a derived neurons limited to the RVLM consistent with previous hypotheses of a distinct, non-catecholaminergic, glutamatergic population in control of blood pressure (Lipski et al., 1995; Schreihofer and Guyenet, 1997).
The proposed pr8 region (Figures 2D,E) contains a continuation of the Lmx1b and Phox2b derived IRt interneurons (Figures 8B, 9D). Ventrolateral to the NTS are glutamatergic neurons of the PCRt and MdD (Figures 8A–C,F). Many of these neurons are Lmx1b, but not Phox2b derived suggesting they may represent a subset of late born neurons derived from the progenitor domain from which the SpV forms (Figures 1B,C) and be similar in development and function to deep dorsal horn glutamatergic neurons (Helms and Johnson, 2003). These neurons extend to the medullary/spinal boundary consistent with this possible developmental origin. Neurons within the region containing dorsal Lmx1b, PCRt population have been implicated in facilitating nociceptive behavior (Almeida et al., 1999). These neurons receive ascending innervation from dorsal horn projection neurons as well as descending input from multiple cortical areas (Almeida and Lima, 1997; Desbois et al., 1999). Previously, neurons within the MdD region been implicated in the eye blink reflex as they express cFos after supraorbital nerve stimulation and project to the orbicularis oculi muscle innervating VII motoneurons (Smit et al., 2006).
Ventral to the scNA are the subset of glutamatergic SST, SST2aR, and NK1R expressing respiratory neurons of the preBötC (Figures 3J, 6D,E). These neurons are a subset of the column of v0v, Dbx1-derived glutamatergic neurons essential for breathing. Recent work suggests this population overlaps the rostral-most region of rhombomere 7, although the exact relationship between preBötC SST neurons and rhombomeric and pseudo-rhombomeric boundaries is still unclear. Most ventrally is the most rostral border of the dA4, Ptf1a derived IO neurons.
One additional population that is most apparent at the pr8 level is a dorsal continuation of glutamatergic v0v, Dbx1-derived neurons that extends toward the dorsal midline (Figures 8B, 9C). At this level, there is a complete segregation between the Dbx1 and Lmx1b populations. This population, however, extends from pr7 to at least pr9. Rostrally, it overlaps with Lmx1b-derived IRt population (Figures 8A,F,G).
The proposed pr9 region (Figures 2F–H) contains several distinct populations. Most dorsal is the Lmx1b and Phox2b expressing Area Postrema (AP, Figures 2F, 4J). The AP includes several distinct subpopulations including a population of hydroxysteroid dehydrogenase 2 and Phox2b expressing, glutamatergic neurons activated by salt-deprivation (Geerling and Loewy, 2008). Ventral to the NTS is a continuation of the Lmx1b derived PCRt and MdD populations that begin in pr8. At this level is the first appearance of a newly described population of Lmx1b-derived, FoxP2 expressing neurons that extends into pr10 (Figures 2F–I, 4B,H). This population of glutamatergic neurons, likely because of its small size and relative sparse distribution, has no currently known function. Based on its location, I hypothesize these neurons are dB3, Lbx1-, and Lmx1b-derived.
The location of the Lmx1b/Phox2b derived dA3, IRt population overlaps with regions previously identified as important for viscerosensory integration. In adult rats and mice, quinine induces strong cFos immunoreactivity in both the NTS and within the ventral IRt population in both GABAergic and non-GABAergic populations (Dinardo and Travers, 1997; Travers et al., 2007). This region receives direct cortical input and is reciprocally connected to gustatory centers within the NTS and parabrachial nuclei (Norgren, 1978; Herbert et al., 1990; Shammah-Lagnado et al., 1992; Dinardo and Travers, 1997; Travers et al., 1997). In total, there are four major dA3, Lmx1b/Phox2b derived populations; the AP, NTS, IRt, and catecholaminergic A1–2/C1–2. Historically, the NTS has been regarded primarily as the way station for transmitting visceral sensory input to higher processing centers. These findings suggest the dA3 population may be capable of much more extensive and independent function than largely assumed.
Within the intermediate reticular formation, the majority of glutamatergic neurons between the NTS dorsally and ventral medullary surface are derived from only two lineages, the Lmx1b- and Phox2b-derived dA3 and the Dbx1-derived v0v. In the ventrolateral medulla these populations overlap with the v0v, Dbx1 neurons being essential for respiratory output and the catecholaminergic and glutamatergic dA3, A1/C1 neurons being important for coordinating responses to stress. Dorsally, these populations overlap in the IRt at the pr7 level, but are clearly segregated at more caudal levels.
Ventral to the dA3, IRt populations lies the stripe of Dbx1-derived neurons, many of which are glutamatergic, v0v neurons (Figures 8A,E). With the pr7 region, this population overlaps with glutamatergic premotor neurons that project to both XII and V motor pools (Dinardo and Travers, 1997). Neurons within this region are strongly rhythmically active during licking but not swallowing and expressed cFos with oral quinine administration (Travers et al., 1997). Within pr8–9, dorsal v0v glutamatergic populations are located in the region known to contain presumptive glutamatergic premotor neurons of the XIIn based on calcium imaging and trans-synaptic labeling experiments (Dobbins and Feldman, 1995; Fay and Norgren, 1997; Koizumi et al., 2008). As these neurons are developmentally related to neurons essential for respiratory rhythm generation, it suggests the Dbx1 population may play an essential role in rhythmic motor output for multiple behaviors, not just breathing (Bouvier et al., 2010; Gray et al., 2010).
The pattern of organization I describe here is, at least in part, consistent with proposals put forward by Johnson over 100 years ago (Johnson, 1902) and which have been recently described in the organization of transmitter populations in zebrafish (Kinkhabwala et al., 2011; Koyama et al., 2011). It is also partially consistent with Nieuwenhuys' topographical description of hindbrain organization (Nieuwenhuys, 2011) with the addition of a more direct testing of the relationship between developmental and adult location. It is important to note, however, that this proposed schematic has several limitations. Dorso-ventrally it is most consistent with populations within the intermediate reticular formation. The ventrolateral medulla, in contrast, shows extensive mixing of multiple developmental populations (dA1, dA3, dB1, dB3, and v0v) while the dorsal medulla contains multiple subpopulations within clearly defined nuclear structures, such as the NTS with some variation at the boundaries depending upon location.
Combined with the discrete progenitor domains present during early development, I hypothesize the medulla is organized into a “reticular lattice” with clear dorso-ventral and rostro-caudal regions of shared development, gene expression, and possibly function. The developmental origins of diverse reticular formation populations can be defined by anatomical location and neurotransmitter phenotype. Broadly, the fate-mapping data described here combined with previous connectivity and activity data from both rats and mice suggest both a genetic and anatomical separation between sensory and motor processing. While Johnson proposed this general hypothesis over a century ago (Johnson, 1902), here I show that the two major glutamatergic lineages, dA3 and v0v, are adjacent to each other, in spite of their distant developmental origins. Whether this linkage between viserosensory and motor outputs is evolutionarily conserved is unknown.
Conflict of Interest Statement
The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
I would like to thank Guang-Yi Ling and George McMurray for technical assistance. I would also like to thank Arthur Loewy for comments on the text, Frank Constantini for Rosa26-YFP mice, Christos Goridis for sharing Phox2b antibody, Alessandra Pierani for Dbx1-βgal mice, David Rowitch for Atoh1-Cre mice, Randy Johnson for Lmx1b-βgal mice, and Christopher Wright for Ptf1a Cre mice. This work was supported by the US National Institutes of Health HL089742 and Australian NHMRC APP102818. This research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Abbreviations
A1/C1, A1/C1 catecholaminergic group; A2/C2, A2/C2 catecholaminergic group; Ach, acetylcholine; AP, area postrema; Ascl1, achaete-scute homolog 1; Atoh1, atonal homolog 1; βgal, beta-galactosidase; bHLHb5, basic helix loop helix b5; BötC, Bötzinger Complex; ChAT, choline acetyltransferase; Chx10, ceh-10 homeodomain containing homolog; cNA, compact Nucleus Ambiguus; Cre, cre-recombinase; Cu, cuneate nucleus; Dbx1, developing brain homeobox 1; DMX, dorsal motor nucleus of the vagus; ECu, external cuneate; En1, engrailed 1; Evx1, evenskipped 1; FoxP2, forkhead box P2; GABA, gamma aminobutyric acid; GAD1, glutamic decarboxylase 1; GATA3, GATA binding protein 3; Glu, glutamate; GFP, green fluorescent protein; Gly, glycine; Gr, gracile nucleus; IO, inferior olive; IRt, internal reticular formation; Lbx1, ladybird homeobox 1; Lhx9, LIM homeobox 9; Li, linear nucleus; Lmx1b, LIM homeobox transcription factor 1 beta; LRN, lateral reticular nucleus; MdD, dorsal reticular nucleus of the medulla; Mo5, trigeminal motor nucleus; MVe, medial vestibular nucleus; MVePC, medial vestibular nucleus parvocellular; Ngn1, neurogenin 1; NKx2.2, NK2 transcription factor related, locus 2; nRO, nucleus of Roller; NA, nucleus ambiguus; NK1R, neurokinin 1 receptor; NTS, nucleus of the tractus solitarius; Olig1, oligodendrocyte transcription factor 1; Pax2, paired box 2; PCRt, parvocellular reticular region; Pet1, plasmacytoma expressed transcript 1; pFRG, parafacial respiratory group; Phox2b, paired-like homeobox 2b; Pitx2, paired-like homeodomain transcription factor 2; Pr, prepositus hypoglossi; Pr7–10, pseudo-rhombomere 7–10; preBötC, preBötzinger Complex; Ptf1a, pancreas specific transcription factor, 1a; Py, pyramidal tract; RMg, raphe magnus; RPa, raphe palidus; ROb, raphe obscurus; RTN, retrotrapezoid nucleus; R26, Rosa26; RVLM, rostroventrolateral medulla; SpV, spinal nucleus of the trigeminal nerve; SpVe, spinal vestibular nucleus; SST, somatostatin; SST2aR, somatostatin 2a receptor; TF, transcription factor; TH, tyrosine hydroxylase; TPH, tryptophan hydroxylase; VII, facial motonucleus; VGlut2, vesicular glutamate transporter 2 (SLC17A6); XII, hypoglossal motonucleus; YFP, yellow fluorescent protein; 5-HT, serotonin.
References
Abbott, S. B., Kanbar, R., Bochorishvili, G., Coates, M. B., Stornetta, R. L., and Guyenet, P. G. (2012). C1 neurons excite locus coeruleus and A5 noradrenergic neurons along with sympathetic outflow in rats. J. Physiol. 590, 2897–2915.
Alenina, N., Bashammakh, S., and Bader, M. (2006). Specification and differentiation of serotonergic neurons. Stem Cell Rev. 2, 5–10.
Almeida, A., Cobos, A., Tavares, I., and Lima, D. (2002). Brain afferents to the medullary dorsal reticular nucleus: a retrograde and anterograde tracing study in the rat. Eur. J. Neurosci. 16, 81–95.
Almeida, A., and Lima, D. (1997). Activation by cutaneous or visceral noxious stimulation of spinal neurons projecting to the medullary dorsal reticular nucleus in the rat: a c-fos study. Eur. J. Neurosci. 9, 686–695.
Almeida, A., Storkson, R., Lima, D., Hole, K., and Tjolsen, A. (1999). The medullary dorsal reticular nucleus facilitates pain behaviour induced by formalin in the rat. Eur. J. Neurosci. 11, 110–122.
Altman, J., and Bayer, S. A. (1980a). Development of the brain stem in the rat. I. Thymidine-radiographic study of the time of origin of neurons of the lower medulla. J. Comp. Neurol. 194, 1–35.
Altman, J., and Bayer, S. A. (1980b). Development of the brain stem in the rat. II. Thymidine-radiographic study of the time of origin of neurons of the upper medulla, excluding the vestibular and auditory nuclei. J. Comp. Neurol. 194, 37–56.
Alvarez, F. J., Jonas, P. C., Sapir, T., Hartley, R., Berrocal, M. C., Geiman, E. J., et al. (2005). Postnatal phenotype and localization of spinal cord V1 derived interneurons. J. Comp. Neurol. 493, 177–192.
Baumgardt, M., Miguel-Aliaga, I., Karlsson, D., Ekman, H., and Thor, S. (2007). Specification of neuronal identities by feedforward combinatorial coding. PLoS Biol. 5:e37. doi: 10.1371/journal.pbio.0050037
Ben-Arie, N., Bellen, H. J., Armstrong, D. L., McCall, A. E., Gordadze, P. R., Guo, Q., et al. (1997). Math1 is essential for genesis of cerebellar granule neurons. Nature 390, 169–172.
Bergquist, H., and Källěn, B. (1954). Notes on the early histogenesis and morphogenesis of the central nervous system in vertebrates. J. Comp. Neurol. 100, 627–659.
Bermingham, N. A., Hassan, B. A., Wang, V. Y., Fernandez, M., Banfi, S., Bellen, H. J., et al. (2001). Proprioceptor pathway development is dependent on Math1. Neuron 30, 411–422.
Bieger, D. (2001). Rhombencephalic pathways and neurotransmitters controlling deglutition. Am. J. Med. 111, 85–89.
Boulland, J. L., Qureshi, T., Seal, R. P., Rafiki, A., Gundersen, V., Bergersen, L. H., et al. (2004). Expression of the vesicular glutamate transporters during development indicates the widespread corelease of multiple neurotransmitters. J. Comp. Neurol. 480, 264–280.
Bouvier, J., Thoby-Brisson, M., Renier, N., Dubreuil, V., Ericson, J., Champagnat, J., et al. (2010). Hindbrain interneurons and axon guidance signaling critical for breathing. Nat. Neurosci. 13, 1066–1074.
Briscoe, J., Pierani, A., Jessell, T. M., and Ericson, J. (2000). A homeodomain protein code specifies progenitor cell identity and neuronal fate in the ventral neural tube. Cell 101, 435–445.
Brodal, A. (1952). Experimental demonstration of cerebellar connexions from the perihypoglossal nuclei (nucleus intercalatus, nucleus praepositus hypoglossal and nucleus of roller) in the cat. J. Anat. 86, 110–129.
Brodal, A. (1957). The Reticular Formation of the Brain Stem: Anatomical Aspects and Functional Correlations. Edinburgh: Oliver and Boyd.
Brohl, D., Strehle, M., Wende, H., Hori, K., Bormuth, I., Nave, K. A., et al. (2008). A transcriptional network coordinately determines transmitter and peptidergic fate in the dorsal spinal cord. Dev. Biol. 322, 381–393.
Brunet, J. F., and Pattyn, A. (2002). Phox2 genes - from patterning to connectivity. Curr. Opin. Gen. Dev. 12, 435–440.
Burke, P. G., Li, Q., Costin, M. L., McMullan, S., Pilowsky, P. M., and Goodchild, A. K. (2008). Somatostatin 2A receptor-expressing presympathetic neurons in the rostral ventrolateral medulla maintain blood pressure. Hypertension 52, 1127–1133.
Burke, P. G., Neale, J., Korim, W. S., McMullan, S., and Goodchild, A. K. (2011). Patterning of somatosympathetic reflexes reveals nonuniform organization of presympathetic drive from C1 and non-C1 RVLM neurons. Am. J. Physiol. Regul. Integr. Comp. Physiol. 301, R1112–R1122.
Cambronero, F., and Puelles, L. (2000). Rostrocaudal nuclear relationships in the avian medulla oblongata: a fate map with quail chick chimeras. J. Comp. Neurol. 427, 522–545.
Chalmers, J., Arnolda, L., Llewellyn-Smith, I., Minson, J., Pilowsky, P., and Suzuki, S. (1994). Central neurons and neurotransmitters in the control of blood pressure. Clin. Exp. Pharmacol. Physiol. 21, 819–829.
Chalmers, J. P., Kapoor, V., Llewellyn-Smith, I. J., Minson, J. B., and Pilowsky, P. M. (1992). Central control of blood pressure. Eur. Heart J. 13, 2–9.
Chattopadhyaya, B., Di Cristo, G., Higashiyama, H., Knott, G. W., Kuhlman, S. J., Welker, E., et al. (2004). Experience and activity-dependent maturation of perisomatic GABAergic innervation in primary visual cortex during a postnatal critical period. J. Neurosci. 24, 9598–9611.
Chen, M. L., and Keens, T. G. (2004). Congenital central hypoventilation syndrome: not just another rare disorder. Paediatr. Respir. Rev. 5, 182–189.
Chen, P., Johnson, J. E., Zoghbi, H. Y., and Segil, N. (2002). The role of Math1 in inner ear development: uncoupling the establishment of the sensory primordium from hair cell fate determination. Development 129, 2495–2505.
Cheng, L., Arata, A., Mizuguchi, R., Qian, Y., Karunaratne, A., Gray, P. A., et al. (2004). Tlx3 and Tlx1 are post-mitotic selector genes determining glutamatergic over GABAergic cell fates. Nat. Neurosci. 7, 510–517.
Cheng, L., Chen, C. L., Luo, P., Tan, M., Qiu, M., Johnson, R., et al. (2003). Lmx1b, Pet-1, and Nkx2.2 coordinately specify serotonergic neurotransmitter phenotype. J. Neurosci. 23, 9961–9967.
Craven, S. E., Lim, K. C., Ye, W., Engel, J. D., De Sauvage, F., and Rosenthal, A. (2004). Gata2 specifies serotonergic neurons downstream of sonic hedgehog. Development 131, 1165–1173.
Crone, S. A., Viemari, J. C., Droho, S., Mrejeru, A., Ramirez, J. M., and Sharma, K. (2012). Irregular breathing in mice following genetic ablation of V2a neurons. J. Neurosci. 32, 7895–7906.
Dampney, R. A., Goodchild, A. K., Robertson, L. G., and Montgomery, W. (1982). Role of ventrolateral medulla in vasomotor regulation: a correlative anatomical and physiological study. Brain Res. 249, 223–235.
Dauger, S., Pattyn, A., Lofaso, F., Gaultier, C., Goridis, C., Gallego, J., et al. (2003). Phox2b controls the development of peripheral chemoreceptors and afferent visceral pathways. Development 130, 6635–6642.
Desbois, C., Le Bars, D., and Villanueva, L. (1999). Organization of cortical projections to the medullary subnucleus reticularis dorsalis: a retrograde and anterograde tracing study in the rat. J. Comp. Neurol. 410, 178–196.
Diez-Roux, G., Banfi, S., Sultan, M., Geffers, L., Anand, S., Rozado, D., et al. (2011). A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol. 9:e1000582. doi: 10.1371/journal.pbio.1000582
Dinardo, L. A., and Travers, J. B. (1997). Distribution of fos-like immunoreactivity in the medullary reticular formation of the rat after gustatory elicited ingestion and rejection behaviors. J. Neurosci. 17, 3826–3839.
Ding, Y. Q., Marklund, U., Yuan, W., Yin, J., Wegman, L., Ericson, J., et al. (2003). Lmx1b is essential for the development of serotonergic neurons. Nat. Neurosci. 6, 933–938.
Ding, Y. Q., Yin, J., Kania, A., Zhao, Z. Q., Johnson, R. L., and Chen, Z. F. (2004). Lmx1b controls the differentiation and migration of the superficial dorsal horn neurons of the spinal cord. Development 131, 3693–3703.
Dobbins, E. G., and Feldman, J. L. (1995). Differential innervation of protruder and retractor muscles of the tongue in rat. J. Comp. Neurol. 357, 376–394.
Dubreuil, V., Hirsch, M. R., Pattyn, A., Brunet, J. F., and Goridis, C. (2000). The Phox2b transcription factor coordinately regulates neuronal cell cycle exit and identity. Development 127, 5191–5201.
Dubreuil, V., Thoby-Brisson, M., Rallu, M., Persson, K., Pattyn, A., Birchmeier, C., et al. (2009). Defective respiratory rhythmogenesis and loss of central chemosensitivity in Phox2b mutants targeting retrotrapezoid nucleus neurons. J. Neurosci. 29, 14836–14846.
Dymecki, S. M., Rodriguez, C. I., and Awatramani, R. B. (2002). Switching on lineage tracers using site-specific recombination. Methods Mol. Biol. 185, 309–334.
Dymecki, S. M., and Tomasiewicz, H. (1998). Using Flp-recombinase to characterize expansion of Wnt1-expressing neural progenitors in the mouse. Dev. Biol. 201, 57–65.
Esser, M. J., Pronych, S. P., and Allen, G. V. (1998). Trigeminal-reticular connections: possible pathways for nociception-induced cardiovascular reflex responses in the rat. J. Comp. Neurol. 391, 526–544.
Fay, R. A., and Norgren, R. (1997). Identification of rat brainstem multisynaptic connections to the oral motor nuclei using pseudorabies virus. I. Masticatory muscle motor systems. Brain Res. Brain Res. Rev. 25, 255–275.
Feldman, J. L., Del Negro, C., and Gray, P. A. (2013). “Understanding the Rhythm of Breathing: So Near, Yet So Far,” in Annual Review of Physiology, Vol. 75, eds D. Julius and D. E. Clapham (Palo Alto: Annual Reviews), 423–452.
Fogarty, M., Richardson, W. D., and Kessaris, N. (2005). A subset of oligodendrocytes generated from radial glia in the dorsal spinal cord. Development 132, 1951–1959.
Franklin, K. B. J. (1997). The Mouse Brain in Stereotaxic Coordinates. San Diego, CA: Academic Press.
Fremeau, R. T. Jr., Voglmaier, S., Seal, R. P., and Edwards, R. H. (2004). VGLUTs define subsets of excitatory neurons and suggest novel roles for glutamate. Trends Neurosci. 27, 98–103.
Fu, Y., Tvrdik, P., Makki, N., Palombi, O., MacHold, R., Paxinos, G., et al. (2009). The precerebellar linear nucleus in the mouse defined by connections, immunohistochemistry, and gene expression. Brain Res. 1271, 49–59.
Garcia-Campmany, L., Stam, F. J., and Goulding, M. (2010). From circuits to behaviour: motor networks in vertebrates. Curr. Opin. Neurobiol. 20, 116–125.
Gaufo, G. O., Thomas, K. R., and Capecchi, M. R. (2003). Hox3 genes coordinate mechanisms of genetic suppression and activation in the generation of branchial and somatic motoneurons. Development 130, 5191–5201.
Gaufo, G. O., Wu, S., and Capecchi, M. R. (2004). Contribution of Hox genes to the diversity of the hindbrain sensory system. Development 131, 1259–1266.
Geerling, J. C., and Loewy, A. D. (2008). Central regulation of sodium appetite. Exp. Physiol. 93, 177–209.
Geerling, J. C., Stein, M. K., Miller, R. L., Shin, J. W., Gray, P. A., and Loewy, A. D. (2011). FoxP2 expression defines dorsolateral pontine neurons activated by sodium deprivation. Brain Res. 1375, 19–27.
Glasgow, S. M., Henke, R. M., MacDonald, R. J., Wright, C. V., and Johnson, J. E. (2005). Ptf1a determines GABAergic over glutamatergic neuronal cell fate in the spinal cord dorsal horn. Development 132, 5461–5469.
Gray, P. A. (2008). Transcription factors and the genetic organization of brain stem respiratory neurons. J. Appl. Physiol. 104, 1513–1521.
Gray, P. A., Fu, H., Luo, P., Zhao, Q., Yu, J., Ferrari, A., et al. (2004). Mouse brain organization revealed through direct genome-scale TF expression analysis. Science 306, 2255–2257.
Gray, P. A., Hayes, J. A., Ling, G. Y., Llona, I., Tupal, S., Picardo, M. C., et al. (2010). Developmental origin of preBotzinger complex respiratory neurons. J. Neurosci. 30, 14883–14895.
Gray, P. A., Rekling, J. C., Bocchiaro, C. M., and Feldman, J. L. (1999). Modulation of respiratory frequency by peptidergic input to rhythmogenic neurons in the preBotzinger complex. Science 286, 1566–1568.
Guyenet, P. G., Schreihofer, A. M., and Stornetta, R. L. (2001). Regulation of sympathetic tone and arterial pressure by the rostral ventrolateral medulla after depletion of C1 cells in rats. Ann. N.Y. Acad. Sci. 940, 259–269.
Guyenet, P. G., Sevigny, C. P., Weston, M. C., and Stornetta, R. L. (2002). Neurokinin-1 receptor-expressing cells of the ventral respiratory group are functionally heterogeneous and predominantly glutamatergic. J. Neurosci. 22, 3806–3816.
Helms, A. W., and Johnson, J. E. (1998). Progenitors of dorsal commissural interneurons are defined by MATH1 expression. Development 125, 919–928.
Helms, A. W., and Johnson, J. E. (2003). Specification of dorsal spinal cord interneurons. Curr. Opin. Neurobiol. 13, 42–49.
Herbert, H., Moga, M. M., and Saper, C. B. (1990). Connections of the parabrachial nucleus with the nucleus of the solitary tract and the medullary reticular formation in the rat. J. Comp. Neurol. 293, 540–580.
Hisano, S., Sawada, K., Kawano, M., Kanemoto, M., Xiong, G., Mogi, K., et al. (2002). Expression of inorganic phosphate/vesicular glutamate transporters (BNPI/VGLUT1 and DNPI/VGLUT2) in the cerebellum and precerebellar nuclei of the rat. Brain Res. Mol. Brain Res. 107, 23–31.
Hoshino, M., Nakamura, S., Mori, K., Kawauchi, T., Terao, M., Nishimura, Y. V., et al. (2005). Ptf1a, a bHLH transcriptional gene, defines GABAergic neuronal fates in cerebellum. Neuron 47, 201–213.
Huang, W. H., Tupal, S., Huang, T. W., Ward, C. S., Neul, J. L., Klisch, T. J., et al. (2012). Atoh1 governs the migration of postmitotic neurons that shape respiratory effectiveness at birth and chemoresponsiveness in adulthood. Neuron 75, 799–809.
Jansen, A. S., Nguyen, X. V., Karpitskiy, V., Mettenleiter, T. C., and Loewy, A. D. (1995). Central command neurons of the sympathetic nervous system: basis of the fight-or-flight response. Science 270, 644–646.
John, A., Wildner, H., and Britsch, S. (2005). The homeodomain transcription factor Gbx1 identifies a subpopulation of late-born GABAergic interneurons in the developing dorsal spinal cord. Dev. Dyn. 234, 767–771.
Johnson, J. B. (1902). An attempt to define the primitive functional divisions of the central nervous system. J. Comp. Neurol. 12, 87–106.
Kalia, M., and Fuxe, K. (1985). Rat medulla oblongata. I. Cytoarchitectonic considerations. J. Comp. Neurol. 233, 285–307.
Kalia, M., Fuxe, K., and Goldstein, M. (1985a). Rat medulla oblongata. II., Dopaminergic, noradrenergic (A1 and A2) and adrenergic neurons, nerve fibers, and presumptive terminal processes. J. Comp. Neurol. 233, 308–332.
Kalia, M., Fuxe, K., and Goldstein, M. (1985b). Rat medulla oblongata. III. Adrenergic (C1 and C2) neurons, nerve fibers and presumptive terminal processes. J. Comp. Neurol. 233, 333–349.
Kalia, M., Woodward, D. J., Smith, W. K., and Fuxe, K. (1985c). Rat medulla oblongata. IV. Topographical distribution of catecholaminergic neurons with quantitative three-dimensional computer reconstruction. J. Comp. Neurol. 233, 350–364.
Kang, B. J., Chang, D. A., MacKay, D. D., West, G. H., Moreira, T. S., Takakura, A. C., et al. (2007). Central nervous system distribution of the transcription factor Phox2b in the adult rat. J. Comp. Neurol. 503, 627–641.
Kawaguchi, Y., Cooper, B., Gannon, M., Ray, M., MacDonald, R. J., and Wright, C. V. (2002). The role of the transcriptional regulator Ptf1a in converting intestinal to pancreatic progenitors. Nat. Genet. 32, 128–134.
Kinkhabwala, A., Riley, M., Koyama, M., Monen, J., Satou, C., Kimura, Y., et al. (2011). A structural and functional ground plan for neurons in the hindbrain of zebrafish. Proc. Natl. Acad. Sci. U.S.A. 108, 1164–1169.
Koizumi, H., Wilson, C. G., Wong, S., Yamanishi, T., Koshiya, N., and Smith, J. C. (2008). Functional imaging, spatial reconstruction, and biophysical analysis of a respiratory motor circuit isolated in vitro. J. Neurosci. 28, 2353–2365.
Koyama, M., Kinkhabwala, A., Satou, C., Higashijima, S., and Fetcho, J. (2011). Mapping a sensory-motor network onto a structural and functional ground plan in the hindbrain. Proc. Natl. Acad. Sci. U.S.A. 108, 1170–1175.
Krumlauf, R., Marshall, H., Studer, M., Nonchev, S., Sham, M. H., and Lumsden, A. (1993). Hox homeobox genes and regionalisation of the nervous system. J. Neurobiol. 24, 1328–1340.
Lai, C. S., Fisher, S. E., Hurst, J. A., Vargha-Khadem, F., and Monaco, A. P. (2001). A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413, 519–523.
Lanuza, G. M., Gosgnach, S., Pierani, A., Jessell, T. M., and Goulding, M. (2004). Genetic identification of spinal interneurons that coordinate left-right locomotor activity necessary for walking movements. Neuron 42, 375–386.
Lein, E. S., Hawrylycz, M. J., Ao, N., Ayres, M., Bensinger, A., Bernard, A., et al. (2007). Genome-wide atlas of gene expression in the adult mouse brain. Nature 445, 168–176.
Leite-Almeida, H., Valle-Fernandes, A., and Almeida, A. (2006). Brain projections from the medullary dorsal reticular nucleus: an anterograde and retrograde tracing study in the rat. Neuroscience 140, 577–595.
Lima, D., and Almeida, A. (2002). The medullary dorsal reticular nucleus as a pronociceptive centre of the pain control system. Prog. Neurobiol. 66, 81–108.
Lipski, J., Kanjhan, R., Kruszewska, B., and Smith, M. (1995). Barosensitive neurons in the rostral ventrolateral medulla of the rat in vivo: morphological properties and relationship to C1 adrenergic neurons. Neuroscience 69, 601–618.
Llona, I., Ampuero, E., and Eugenin, J. L. (2004). Somatostatin inhibition of fictive respiration is modulated by pH. Brain Res. 1026, 136–142.
Llona, I., and Eugenin, J. (2005). Central actions of somatostatin in the generation and control of breathing. Biol. Res. 38, 347–352.
Lumpkin, E. A., Collisson, T., Parab, P., Omer-Abdalla, A., Haeberle, H., Chen, P., et al. (2003). Math1-driven GFP expression in the developing nervous system of transgenic mice. Gene Expr. Patterns 3, 389–395.
Machold, R., Klein, C., and Fishell, G. (2011). Genes expressed in Atoh1 neuronal lineages arising from the r1/isthmus rhombic lip. Gene Expr. Patterns 11, 349–359.
Madden, C. J., and Sved, A. F. (2003). Cardiovascular regulation after destruction of the C1 cell group of the rostral ventrolateral medulla in rats. Am. J. Physiol. Heart Circ. Physiol. 285, H2734–H2748.
Manzanares, M., Nardelli, J., Gilardi-Hebenstreit, P., Marshall, H., Giudicelli, F., Martinez-Pastor, M. T., et al. (2002). Krox20 and kreisler co-operate in the transcriptional control of segmental expression of Hoxb3 in the developing hindbrain. EMBO J. 21, 365–376.
Manzanares, M., Trainor, P. A., Nonchev, S., Ariza-McNaughton, L., Brodie, J., Gould, A., et al. (1999). The role of kreisler in segmentation during hindbrain development. Dev. Biol. 211, 220–237.
Marin, F., Aroca, P., and Puelles, L. (2008). Hox gene colinear expression in the avian medulla oblongata is correlated with pseudorhombomeric domains. Dev. Biol. 323, 230–247.
McCrea, R. A., Baker, R., and Delgado-Garcia, J. (1979). Afferent and efferent organization of the prepositus hypoglossi nucleus. Prog. Brain Res. 50, 653–665.
Miesegaes, G. R., Klisch, T. J., Thaller, C., Ahmad, K. A., Atkinson, R. C., and Zoghbi, H. Y. (2009). Identification and subclassification of new Atoh1 derived cell populations during mouse spinal cord development. Dev. Biol. 327, 339–351.
Miles, G. B., Hartley, R., Todd, A. J., and Brownstone, R. M. (2007). Spinal cholinergic interneurons regulate the excitability of motoneurons during locomotion. Proc. Natl. Acad. Sci. U.S.A. 104, 2448–2453.
Miles, G. B., and Sillar, K. T. (2011). Neuromodulation of vertebrate locomotor control networks. Physiology 26, 393–411.
Miller, R. L., Knuepfer, M. M., Wang, M. H., Denny, G. O., Gray, P. A., and Loewy, A. D. (2012). Fos-activation of FoxP2 and Lmx1b neurons in the parabrachial nucleus evoked by hypotension and hypertension in conscious rats. Neuroscience 218, 113–125.
Miller, R. L., Stein, M. K., and Loewy, A. D. (2011). Serotonergic inputs to FoxP2 neurons of the pre-locus coeruleus and parabrachial nuclei that project to the ventral tegmental area. Neuroscience 193, 229–240.
Moran-Rivard, L., Kagawa, T., Saueressig, H., Gross, M. K., Burrill, J., and Goulding, M. (2001). Evx1 is a postmitotic determinant of v0 interneuron identity in the spinal cord. Neuron 29, 385–399.
Nichols, D. H., and Bruce, L. L. (2006). Migratory routes and fates of cells transcribing the Wnt-1 gene in the murine hindbrain. Dev. Dyn. 235, 285–300.
Nieuwenhuys, R. (2011). The structural, functional and molecular organization of the brainstem. Front. Neuroanat. 5:33. doi: 10.3389/fnana.2011.00033
Nikundiwe, A. M., and Nieuwenhuys, R. (1983). The cell masses in the brainstem of the South African clawed frog Xenopus laevis: a topographical and topological analysis. J. Comp. Neurol. 213, 199–219.
Norgren, R. (1978). Projections from the nucleus of the solitary tract in the rat. Neuroscience 3, 207–218.
Pagliardini, S., Ren, J., Gray, P. A., Vandunk, C., Gross, M., Goulding, M., et al. (2008). Central respiratory rhythmogenesis is abnormal in lbx1- deficient mice. J. Neurosci. 28, 11030–11041.
Pattyn, A., Goridis, C., and Brunet, J. F. (2000a). Specification of the central noradrenergic phenotype by the homeobox gene Phox2b. Mol. Cell. Neurosci. 15, 235–243.
Pattyn, A., Hirsch, M., Goridis, C., and Brunet, J. F. (2000b). Control of hindbrain motor neuron differentiation by the homeobox gene Phox2b. Development 127, 1349–1358.
Pattyn, A., Morin, X., Cremer, H., Goridis, C., and Brunet, J. F. (1997). Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis. Development 124, 4065–4075.
Pattyn, A., Morin, X., Cremer, H., Goridis, C., and Brunet, J. F. (1999). The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives. Nature 399, 366–370.
Pattyn, A., Simplicio, N., Van Doorninck, J. H., Goridis, C., Guillemot, F., and Brunet, J. F. (2004). Ascl1/Mash1 is required for the development of central serotonergic neurons. Nat. Neurosci. 7, 589–595.
Pierani, A., Moran-Rivard, L., Sunshine, M. J., Littman, D. R., Goulding, M., and Jessell, T. M. (2001). Control of interneuron fate in the developing spinal cord by the progenitor homeodomain protein Dbx1. Neuron 29, 367–384.
Pilowsky, P. M. (2008). Neurochemical phenotypes of cardiorespiratory neurons. Respir. Physiol. Neurobiol. 164, 12–17.
Pilowsky, P. M., Lung, M. S., Spirovski, D., and McMullan, S. (2009). Differential regulation of the central neural cardiorespiratory system by metabotropic neurotransmitters. Philos. Trans. R. Soc. Lond. B Biol. Sci. 364, 2537–2552.
Prasad, T., Wang, X., Gray, P. A., and Weiner, J. A. (2008). A differential developmental pattern of spinal interneuron apoptosis during synaptogenesis: insights from genetic analyses of the protocadherin-gamma gene cluster. Development 135, 4153–4164.
Pressman, C. L., Chen, H., and Johnson, R. L. (2000). LMX1B, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye. Genesis 26, 15–25.
Qian, Y., Fritzsch, B., Shirasawa, S., Chen, C. L., Choi, Y., and Ma, Q. (2001). Formation of brainstem (nor)adrenergic centers and first-order relay visceral sensory neurons is dependent on homeodomain protein Rnx/Tlx3. Genes Dev. 15, 2533–2545.
Qian, Y., Shirasawa, S., Chen, C. L., Cheng, L., and Ma, Q. (2002). Proper development of relay somatic sensory neurons and D2/D4 interneurons requires homeobox genes Rnx/Tlx-3 and Tlx-1. Genes Dev. 16, 1220–1233.
Ramanantsoa, N., Hirsch, M. R., Thoby-Brisson, M., Dubreuil, V., Bouvier, J., Ruffault, P. L., et al. (2011). Breathing without CO(2) chemosensitivity in conditional Phox2b mutants. J. Neurosci. 31, 12880–12888.
Ray, R. S., Corcoran, A. E., Brust, R. D., Kim, J. C., Richerson, G. B., Nattie, E., et al. (2011). Impaired respiratory and body temperature control upon acute serotonergic neuron inhibition. Science 333, 637–642.
Rivkin, E., and Cordes, S. P. (2008). Generation of a transgenic mouse line expressing GFP-Cre protein from a Hoxb4 neural enhancer. Genesis 46, 119–124.
Rose, M. F., Ahmad, K. A., Thaller, C., and Zoghbi, H. Y. (2009a). Excitatory neurons of the proprioceptive, interoceptive, and arousal hindbrain networks share a developmental requirement for Math1. Proc. Natl. Acad. Sci. U.S.A. 106, 22462–22467.
Rose, M. F., Ren, J., Ahmad, K. A., Chao, H. T., Klisch, T. J., Flora, A., et al. (2009b). Math1 is essential for the development of hindbrain neurons critical for perinatal breathing. Neuron 64, 341–354.
Ruiz i Altaba, A., and Jessell, T. M. (1991). Retinoic acid modifies the pattern of cell differentiation in the central nervous system of neurula stage Xenopus embryos. Development 112, 945–958.
Schindler, M., Sellers, L. A., Humphrey, P. P., and Emson, P. C. (1997). Immunohistochemical localization of the somatostatin SST2(A) receptor in the rat brain and spinal cord. Neuroscience 76, 225–240.
Schreihofer, A. M., and Guyenet, P. G. (1997). Identification of C1 presympathetic neurons in rat rostral ventrolateral medulla by juxtacellular labeling in vivo. J. Comp. Neurol. 387, 524–536.
Shammah-Lagnado, S. J., Costa, M. S., and Ricardo, J. A. (1992). Afferent connections of the parvocellular reticular formation: a horseradish peroxidase study in the rat. Neuroscience 50, 403–425.
Shao, X. M., and Feldman, J. L. (2009). Central cholinergic regulation of respiration: nicotinic receptors. Acta Pharmacol. Sin. 30, 761–770.
Shin, J. W., Geerling, J. C., Stein, M. K., Miller, R. L., and Loewy, A. D. (2011). FoxP2 brainstem neurons project to sodium appetite regulatory sites. J. Comp. Neurol. 42, 1–23.
Sieber, M. A., Storm, R., Martinez-de-la-Torre, M., Muller, T., Wende, H., Reuter, K., et al. (2007). Lbx1 acts as a selector gene in the fate determination of somatosensory and viscerosensory relay neurons in the hindbrain. J. Neurosci. 27, 4902–4909.
Smit, A. E., Buisseret, P., Buisseret-Delmas, C., De Zeeuw, C. I., Vanderwerf, F., and Zerari-Mailly, F. (2006). Reticulo-collicular and spino-collicular projections involved in eye and eyelid movements during the blink reflex. Neurosci. Res. 56, 363–371.
Srinivas, S., Watanabe, T., Lin, C. S., William, C. M., Tanabe, Y., Jessell, T. M., et al. (2001). Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus. BMC Dev. Biol. 1:4. doi: 10.1186/1471-213X-1-4
Stein, M. K., and Loewy, A. D. (2010). Area postrema projects to FoxP2 neurons of the pre-locus coeruleus and parabrachial nuclei: brainstem sites implicated in sodium appetite regulation. Brain Res. 1359, 116–127.
Storm, R., Cholewa-Waclaw, J., Reuter, K., Brohl, D., Sieber, M., Treier, M., et al. (2009). The bHLH transcription factor Olig3 marks the dorsal neuroepithelium of the hindbrain and is essential for the development of brainstem nuclei. Development 136, 295–305.
Stornetta, R. L., Macon, C. J., Nguyen, T. M., Coates, M. B., and Guyenet, P. G. (2012). Cholinergic neurons in the mouse rostral ventrolateral medulla target sensory afferent areas. Brain Struct. Funct. 218, 455–475.
Stornetta, R. L., Rosin, D. L., Simmons, J. R., McQuiston, T. J., Vujovic, N., Weston, M. C., et al. (2005). Coexpression of vesicular glutamate transporter-3 and gamma-aminobutyric acidergic markers in rat rostral medullary raphe and intermediolateral cell column. J. Comp. Neurol. 492, 477–494.
Stornetta, R. L., Rosin, D. L., Wang, H., Sevigny, C. P., Weston, M. C., and Guyenet, P. G. (2003). A group of glutamatergic interneurons expressing high levels of both neurokinin-1 receptors and somatostatin identifies the region of the pre-Botzinger complex. J. Comp. Neurol. 455, 499–512.
Stornetta, R. L., Sevigny, C. P., and Guyenet, P. G. (2002a). Vesicular glutamate transporter DNPI/VGLUT2 mRNA is present in C1 and several other groups of brainstem catecholaminergic neurons. J. Comp. Neurol. 444, 191–206.
Stornetta, R. L., Sevigny, C. P., Schreihofer, A. M., Rosin, D. L., and Guyenet, P. G. (2002b). Vesicular glutamate transporter DNPI/VGLUT2 is expressed by both C1 adrenergic and nonaminergic presympathetic vasomotor neurons of the rat medulla. J. Comp. Neurol. 444, 207–220.
Strack, A. M., Sawyer, W. B., Hughes, J. H., Platt, K. B., and Loewy, A. D. (1989). A general pattern of CNS innervation of the sympathetic outflow demonstrated by transneuronal pseudorabies viral infections. Brain Res. 491, 156–162.
Travers, J. B., Dinardo, L. A., and Karimnamazi, H. (1997). Motor and premotor mechanisms of licking. Neurosci. Biobehav. Rev. 21, 631–647.
Travers, J. B., Herman, K., Yoo, J., and Travers, S. P. (2007). Taste reactivity and Fos expression in GAD1-EGFP transgenic mice. Chem. Senses 32, 129–137.
Travers, J. B., Yoo, J. E., Chandran, R., Herman, K., and Travers, S. P. (2005). Neurotransmitter phenotypes of intermediate zone reticular formation projections to the motor trigeminal and hypoglossal nuclei in the rat. J. Comp. Neurol. 488, 28–47.
Tsuda, H., Jafar-Nejad, H., Patel, A. J., Sun, Y., Chen, H. K., Rose, M. F., et al. (2005). The AXH domain of Ataxin-1 mediates neurodegeneration through its interaction with Gfi-1/Senseless proteins. Cell 122, 633–644.
Vanderhorst, V. G., and Ulfhake, B. (2006). The organization of the brainstem and spinal cord of the mouse: relationships between monoaminergic, cholinergic, and spinal projection systems. J. Comp. Neurol. 31, 2–36.
Vandunk, C., Hunter, L. A., and Gray, P. A. (2011). Development, maturation, and necessity of transcription factors in the mouse suprachiasmatic nucleus. J. Neurosci. 31, 6457–6467.
Varner, K. J., Vasquez, E. C., and Brody, M. J. (1994). Lesions in rostral ventromedial or rostral ventrolateral medulla block neurogenic hypertension. Hypertension 24, 91–96.
Voiculescu, O., Taillebourg, E., Pujades, C., Kress, C., Buart, S., Charnay, P., et al. (2001). Hindbrain patterning: Krox20 couples segmentation and specification of regional identity. Development 128, 4967–4978.
Wang, V. Y., Rose, M. F., and Zoghbi, H. Y. (2005). Math1 expression redefines the rhombic lip derivatives and reveals novel lineages within the brainstem and cerebellum. Neuron 48, 31–43.
Yamada, M., Terao, M., Terashima, T., Fujiyama, T., Kawaguchi, Y., Nabeshima, Y., et al. (2007). Origin of climbing fiber neurons and their developmental dependence on Ptf1a. J. Neurosci. 27, 10924–10934.
Yang, C., Kim, H. S., Seo, H., Kim, C. H., Brunet, J. F., and Kim, K. S. (1998). Paired-like homeodomain proteins, Phox2a and Phox2b, are responsible for noradrenergic cell-specific transcription of the dopamine beta-hydroxylase gene. J. Neurochem. 71, 1813–1826.
Zagoraiou, L., Akay, T., Martin, J. F., Brownstone, R. M., Jessell, T. M., and Miles, G. B. (2009). A cluster of cholinergic premotor interneurons modulates mouse locomotor activity. Neuron 64, 645–662.
Zhang, M., Wang, Y. T., Vyas, D. M., Neuman, R. S., and Bieger, D. (1983). Nicotinic cholinoceptor-mediated excitatory postsynaptic potentials in rat nucleus ambiguus. Exp. Brain Res. 96, 83–88.
Keywords: brainstem, transcription factors, reticular formation, fate-mapping, development, rhombomeres, hindbrain
Citation: Gray PA (2013) Transcription factors define the neuroanatomical organization of the medullary reticular formation. Front. Neuroanat. 7:7. doi: 10.3389/fnana.2013.00007
Received: 30 January 2013; Paper pending published: 27 February 2013;
Accepted: 19 April 2013; Published online: 14 May 2013.
Edited by:
Kathleen S. Rockland, MIT, USACopyright © 2013 Gray. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
*Correspondence: Paul A. Gray, Department of Anatomy and Neurobiology, Washington University School of Medicine, Box 8108, 660 S. Euclid Ave., St. Louis, MO 63110, USA. e-mail: pgray@pcg.wustl.edu