Foxb1 Regulates Negatively the Proliferation of Oligodendrocyte Progenitors

Oligodendrocyte precursor cells (OPC), neurons and astrocytes share a neural progenitor cell (NPC) in the early ventricular zone (VZ) of the embryonic neuroepithelium. Both switch to produce either of the three cell types and the generation of the right number of them undergo complex genetic regulation. The components of these regulatory cascades vary between brain regions giving rise to the unique morphological and functional heterogeneity of this organ. Forkhead b1 (Foxb1) is a transcription factor gene expressed by NPCs in specific regions of the embryonic neuroepithelium. We used the mutant mouse line Foxb1-Cre to analyze the cell types derived from Fobx1-expressing NPCs (the Foxb1 cell lineage) from two restricted regions, the medulla oblongata (MO; hindbrain) and the thalamus (forebrain), of normal and Foxb1-deficient mice. Foxb1 cell lineage derivatives appear as clusters in restricted regions, including the MO (hindbrain) and the thalamus (forebrain). Foxb1-expressing NPCs produce mostly oligodendrocytes (OL), some neurons and few astrocytes. Foxb1-deficient NPCs generate mostly OPC and immature OL to the detriment of neurons, astrocytes and mature OL. The axonal G-ratio however is not changed. We reveal Foxb1 as a novel modulator of neuronal and OL generation in certain restricted CNS regions. Foxb1 biases NPCs towards neuronal generation and inhibits OPC proliferation while promoting their differentiation.


INTRODUCTION
Oligodendrocytes (OL) produce and maintain the myelin sheaths around axons of the central nervous system (CNS). In addition, OL can also provide trophic support to axons and promote their viability (Emery, 2010;Mitew et al., 2014). Defects in myelination, the process by which OL wrap axons in layers of myelin, cause severe pathological conditions in humans. In addition, pathological conditions affecting the maturation of the brain white matter in premature infants are on the rise, and their most common result is mental retardation. Since myelination occurs mostly during CNS development, much research has focused on the development of OL. In particular, the mechanisms regulating the proliferation and differentiation of OL, the cells responsible for the formation of the white matter, are currently under intense scrutiny (Goldman and Kuypers, 2015;Marinelli et al., 2016).
OL generate from bipolar, migratory oligodendrocyte progenitor cells (OPC), probably heterogeneous in morphology and physiology, that arise from specific zones of the neuroepithelium ventricular zone (VZ). OPC are identified by the expression of a series of specific antigens, including NG2 chondroitin sulfate proteoglycan (NG2), platelet-derived growth factor-alpha receptor (PDGFRα) and oligodendrocyte transcription factor 2 (Olig2). The OPC specifically express a number of transcription factors as they migrate to colonize the CNS and produce OL. Each phase in the development of OL (OPC, premyelinating OL and myelinating OL) is associated with intense expression of specific sets of transcription factors; once at the final destination, OL mature and acquire the expression of specific markers: MBP, PLP, MAG and Claudin11 among others and acquire their typical morphology as well as the ability to myelinate (Noll and Miller, 1993;Rowitch and Kriegstein, 2010;de Castro et al., 2013;Goldman and Kuypers, 2015). A key point in this pathway, the decision by the OPC to stop proliferating and start producing OL, is under strong control (Dugas et al., 2010).
There are different dorsal and ventral VZ specific areas generating OPC in the hindbrain (Davies and Miller, 2001;Vallstedt et al., 2005). Here we report expression of transcription factor gene Forkhead b1 (Foxb1) in one of the ventral OPC-generating regions in the hindbrain. Foxb1 belongs to a gene family encoding hundreds of transcription factors whose DNA binding domain has a winged helix configuration (Weigel and Jäckle, 1990;Carlsson and Mahlapuu, 2002). Foxb1 is expressed widespread in the early developing VZ of the neural tube and is later restricted to areas of the spinal cord, hindbrain, thalamus and hypothalamus (Ang et al., 1993;Kaestner et al., 1993Kaestner et al., , 1996Alvarez-Bolado et al., 1999;Zhao et al., 2007). Involvement of Foxb1 in OL development has not been reported.
Here we use a Foxb1-Cre knockin-knockout mouse line together with reporter mouse lines Z/AP and ROSA26R in order to approach the following questions: (1) Which specific cell types of the CNS are generated by Foxb1-expressing VZ (i.e., what is the Foxb1 cell lineage in the brain)? (2) What is the role of Foxb1 in oligodendrocyte development? Our results show that Foxb1 is a novel player in OL development, whose role involves inhibiting OPC proliferation and promoting oligodendrocyte maturation.

Mouse Handling
All mouse lines were housed and fed according to the German Animal Welfare Act (Tierschutzgesetz) and the European Communities Council Directive in the Interfacultary Biomedical Facility (IBF), University of Heidelberg. The authorization for collecting mice brain and handling animal samples was approved by the Regierungspraesidium Karlsruhe, Baden-Wuerttemberg. The experiments were carried out in the Neuroanatomy Department, University of Heidelberg and all the procedures were performed according to the Animal Welfare Act. Adult mice were killed by cervical dislocation. The staining protocol for some antibodies required mice to be anesthetized with isofluorane and then intracardially perfused with fixative. For embryos, pregnant mice were sacrificed by cervical dislocation and E12.5, E15.5 or E18.5 pups were taken out of the uterus and processed for histology.

Foxb1-Cre Mouse Line
In this mouse line, transcriptional activation of the Foxb1 locus initiates expression of Cre recombinase and enhanced green fluorescent protein (EGFP; as well as Foxb1 itself in heterozygotes; Zhao et al., 2007Zhao et al., , 2008.

Z/AP Reporter Mouse Line
In Foxb1 Cre x Z/AP mice, Foxb1-expressing cells and their progeny permanently express human placental alkaline phosphatase (hPLAP; Lobe et al., 1999). hPLAP is a GPI-linked cell surface marker. In this reporter line, cells not expressing Cre recombinase are labeled by expression of β-galactosidase (negative control).

ROSA26R Mouse Reporter Line
When dealing with antibodies detecting proteins enriched in the cell nucleus (for instance, transcription factors, like Olig2), the use of a lineage reporter also expressed in the cell nucleus makes it easier to ascertain cellular colocalization of both marker and reporter. ROSA26R (Soriano, 1999) is such a reporter mouse line, carrying β-galactosidase as reporter gene; upon Cre recombination, antibody detection of β-galactosidase produces a characteristic punctate pattern in the cell nucleus (Soriano, 1999). In Foxb1 Cre x ROSA26R mice the presence of β-galactosidase in the nucleus of Cre-expressing cells can be detected from E8.5 on (Zhao et al., 2007(Zhao et al., , 2008.

Labeling Alkaline Phosphatase Activity
Phosphatase/NBT staining has been described (Lobe et al., 1999;Gierut et al., 2014). Briefly, brains or embryos were dissected in PBS buffer on ice; fixed in 4% paraformaldehyde solution with 0.02% NP-40 and 0.01% sodium deoxycholate at 4 • C for 30 min; washed in PBS three times for 30 min at 4 • C; incubated in PBS at 72 • C for 30 min to inactivate endogenous alkaline phosphatase; rinsed three times in PBS for 10 min at room temperature; washed in alkaline phosphatase buffer two times 10 min; stained with 100 mg/ml NBT and 50 mg/ml BCIP in AP buffer at 4 • C until optimal results appeared; washed in PBS extensively to reduce the background; mounted in Mowiol.

Labeling of Thalamic Neurons through Transfection with Two-Reporter Construct
We cloned a DNA construct carrying a constitutive GFP reporter and a Cre-recombination-dependent tdTomato reporter. Every cell transfected will express the green GFP reporter, but transfected cells expressing Cre will express the red tdTomato reporter instead. Our construct was based on MSCV FLIPi P2G_Thy1.1 Dbl (p53, PTEN), a gift from Richard Hynes (Addgene plasmid #19746; Stern et al., 2008). We introduced the following modifications for our purposes: (1) removal of the cassette Puromycin 2a-GFP-Thy1.1-miR-WRPE; (2) insertion of the reporter tdTomato in reverse orientation in the place of Thy1.1-miR; (3) addition of the CAG promoter. The resulting DNA construct was transfected into the thalamus of E12.5 wild type mice through in utero electroporation. The electroporation technique has been described before (Tabata and Nakajima, 2001;Haddad-Tóvolli et al., 2013).

Proliferation Assay
For proliferation studies, 50 mg/kg of body weight of Bromodeoxy-uridine (BrdU) was intraperitoneally injected as aqueous solution into P10 mice three times, at 4 h intervals (Bu et al., 2004). Mice were sacrificed 2 h after the last injection. The brains were dissected and fixed in 4% PFA overnight at 4 • C, washed in PBS for 4-6 h, cryoprotected in 0.1 M PBS containing 30% sucrose, embedded in OCT compound on Dry Ice and stored at −80 • C. Previous to immunodetection of BrdU and Olig2, cryosections (20 µm) were incubated in 1 M HCl for 10 min on ice and then in 2 M HCl for 30 min at 37 • C and neutralized with 0.1 M sodium borate buffer at room temperature.

Confocal Microscope
The results were observed and analyzed under a confocal laserscanning microscope (Zeiss LSM 510) with ZEN 2010 software.

Electron Microscopy and G-Ratio
The G-ratio was calculated on measurements performed on electron microscopy photographs of transverse sections of medulla oblongata (MO). The tissue samples were obtained from Foxb1 Cre/+ and Foxb1 Cre/Cre mouse brains (age P56, three mice per genotype), then processed according to current electron microscopy protocols. The diameter of 80 randomly chosen axons and the corresponding fibers (axon + myelin) were measured for each individual mouse. The data were analyzed with the Mann-Whitney test.

Statistical Analysis
Cell countings were performed on 20 µm sections from the brains of three animals per genotype. Sagittal sections were cut in four series (A, B, C and D) from an area spanning the middle (rostro-caudally) of the hindbrain. Eight sections were counted per mouse. The counting bin for marker-labeled cells was 600 µm × 600 µm in MO. The counting bin for Olig2 plus BrdU was 0.1 mm 2 in MO. The localization of the bins was chosen randomly. Statistical assessment was performed with Prism 5 software (GraphPad Software, San Diego, CA, USA). The Mann-Whitney test was used and the results are represented in bar graphs with mean ± SD; * p < 0.05, * * p < 0.01, * * * p < 0.005.

Foxb1 Is Expressed in Oligodendrocyte-Generating Regions of the Embryonic Hindbrain
Foxb1 is expressed in two narrow longitudinal bands in the VZ of the brainstem (Alvarez-Bolado et al., 1999) reminiscent of the domains of expression of OPC marker genes Olig1 and Olig2 . We asked if the lineage of the Foxb1-expressing neuroepithelium included OL and if Foxb1 was involved in oligodendrocyte development. We approached this question by using a lineage-labeling mouse line, the Foxb1-Cre-EGFP x Z/AP. Foxb1-Cre-EGFP is a knockin-knockout of the Cre recombinase and the expression reporter EGFP into the Foxb1 locus (Zhao et al., 2007). By crossing these lines with the Z/AP reporter line (Lobe et al., 1999), Foxb1-expressing neuroepithelial cells as well as their entire progeny (even if they do not express Foxb1) will permanently express hPLAP in this way becoming identifiable. First, we examined the brains of mouse embryos heterozygous for this insertion. Foxb1-heterozygotes have normal phenotype (Dou et al., 1997;Alvarez-Bolado et al., 2000;Kloetzli et al., 2001) and were used here as proxies for the wild type. Treating early embryonic brains with a procedure to detect alkaline phosphatase activity, we detected as expected the bands in the hindbrain (Figures 1A-C). Later in development, we detected AP+ cells in the MO ( Figure 1D).
By staining MO sections of these mice for hPLAP, we labeled large groups of cells with multiple processes in brains of every developmental age ( Figure 2). As development proceeds, Foxb1-lineage cells form clusters in the brainstem as well as axon-like structures (Figures 2A-C). An internal control is built in the reporter mouse Z/AP (Lobe et al., 1999), so that cells not undergoing a Cre recombination (i.e., not expressing the Cre driver, in this case Foxb1) express β-galactosidase as a reporter instead. We labeled expression of both markers on brainstem sections to confirm that the hPLAP-expressing clusters did not overlap with β-galactosidase-expressing regions (Figures 2D-F).

The Foxb1 Lineage Includes Neurons as well as Large Numbers of Oligodendrocytes
In order to identify the cellular components of these clusters, we colocalized hPLAP with neuron-specific markers (either β-tubulin-III or NeuN) on Foxb1 Cre/+ x Z/AP brains and found a number of double-labeled cells (Figures 3A-F). We confirmed this on primary culture of Foxb1 Cre/+ x Z/AP brain cells (Figures 3G-I). Colocalizing astrocyte-specific protein glial fibrillary acidic protein (GFAP) with hPLAP also showed a small  number of Foxb1-lineage astrocytes (not shown). As expected, no hPLAP-labeled cells expressed microglial marker Iba-1, since microglia originates outside of the neural tube and therefore far from the Foxb1-expressing neuroepithelium (not shown).
The finding that only small numbers of hPLAP-labeled brain cells were neurons or astrocytes suggested that the  Figures 4A-C), in principle confirming this impression. The appearance of the tissue was however complex and did not provide appropriate cellular resolution (Figures 4A-C). Expression of Claudin11, a marker of mature OL (Bronstein et al., 2000), colocalized with profiles morphologically similar to myelinated axons (Figures 4D-F). On primary cultures of cells from the MO of Foxb1 Cre/+ x Z/AP mice, Claudin11 and hPLAP colocalized on cells with unequivocal mature oligodendrocyte morphology, including the characteristic lamellae (Figures 4G-I). Expression of Galactocerebroside C (GalC), a marker of mature as well as immature OL, also colocalized with hPLAP on sections (Figures 4J-L) and on primary cultures (Figures 4M-O).

Foxb1-Lineage
If most of the observed Foxb1-lineage brain cells are OL, it follows that some OPC must also belong to this lineage. To confirm this, we colocalized Foxb1-lineage reporters with OPC markers Olig2 and NG2 (Figure 5). Since Olig2 protein localizes to the cell nucleus, in order to colocalize it with a reporter we crossed our Foxb1 Cre/+ x Z/AP mice with the reporter mouse line ROSA26R (Soriano, 1999), whose cells express β-galactosidase as reporter upon Cre recombination. We found numerous cells expressing both this reporter and Olig2 (Figures 5A-C) in the MO of Foxb1 Cre/+ x ROSA26R mice. The β subunit of the receptor for PDGFRβ as well as NG2 specifically colocalize in OPC (Richardson et al., 1988;Hart et al., 1989). We found also many cells where NG2 colocalized with hPLAP in histological sections of the MO (Figures 5G-I) as well as in culture (Figures 5J-L; see cell abundance quantitation below, Figure 8).

Foxb1-Lineage Cell Clusters
OPC originate from certain spatially restricted regions of the neural tube. They then migrate and proliferate to supply the entire CNS with OL. A current question concerns the possibility that OL from different origins have differential properties and if OL from any given region can be used to substitute for OL in any other region of the brain (replacement therapy). In this context, we asked if the basic composition of the Foxb1 lineage in the hindbrain was similar to that of another regionally restricted subpopulation of Foxb1-lineage brain cells situated not in the hindbrain but in the forebrain. The thalamus is a forebrain region with strong Foxb1 developmental expression and a large part of the thalamus is of Foxb1 lineage (Zhao et al., 2007(Zhao et al., , 2008. Clusters expressing hPLAP were obvious in the thalamus ( Figure 6A). A characteristic property of the thalamus with important functional consequences is the presence of many neurons sending axonal projections to the cortex. We used in utero electroporation with a plasmid expressing upon Cre recombination the red reporter tdTomato (see ''Materials and Methods'' Section for details), which fills the cell body and axons. The results showed abundant Foxb1-lineage thalamo-cortical neurons ( Figure 6B). We confirmed the presence of OL, neurons and astrocytes colocalizing hPLAP on primary thalamic culture (Figures 6C-K; see cell abundance quantitation below, Figure 9).

The Foxb1-Lineage in Foxb1 Mutant Mice Produces Abnormally Large Numbers of OPC
Comparison of Foxb1 Cre/+ x Z/AP and Foxb1 Cre/Cre x Z/AP mouse brains after whole mount histochemical demonstration of AP activity showed very increased staining in the homozygotes (Figures 7A-D). This suggested that Foxb1 had an influence on the cell abundance and maybe also identity. To investigate this, we performed cell countings on tissue of heterozygotes and homozygotes labeled with specific cell markers as well as hPLAP. Our results show, first, that in homozygotes there are more Foxb1-lineage cells (Figure 8A). We also found that, in homozygotes, Foxb1-lineage neurons, astrocytes and mature OL were reduced (Figures 8B-E). However, OPC were increased (Figures 8F,G). Interestingly, a first approach to the abundance of different Foxb1-lineage cell types in the thalamus yielded similar results (Figures 9A-D). This suggests that all Foxb1lineage OL are functionally homogeneous.
Although the exact proportion of Foxb1-lineage cells to other brain cells is not central to our study, we thought it was of some interest to obtain at least a rough approximation to this value for neurons, OL and OPC. Therefore we counted non-hPLAP  (i.e., non-Foxb1-lineage) cell in the bins used to quantitate the hPLAP-expressing (Foxb1-lineage) cells. The results are as follows: (1) mature plus immature OL (i.e., GalC-expressing cells) belonging to the Foxb1-lineage are 73.17% of the total GalC-positive cells per bin in heterozygotes, and 90.00% in homozygotes; (2) OPC (i.e., NG2-expressing cells) belonging to the Foxb1-lineage are 45.40% of all NG2-positive cells per bin in heterozygotes and 75.89% in homozygotes; and (3) neurons (i.e., cells expressing beta-tubulin III) belonging to the Foxb1lineage are 30% of all beta-tubulin III-expressing cells per bin in heterozygotes and 24.78% in homozygotes. As could be expected, OL and OPC of the Foxb1 lineage ''crowd out'' the non-Foxb1 lineage ones in homozygotes, while the proportion of Foxb1- lineage neurons becomes slightly smaller. These data however cannot be directly compared to our cell countings summarized in Figure 10, since those are represented in percent of hPLAPexpressing cells (as opposed to percent of all cells in the bin).
We concluded that, in the Foxb1-deficient MO, the OPC increase to the expense of neurons and mature OL (Figure 10).

OPC Proliferation Increased in Foxb1 Homozygotes
In order to confirm this increase in OPC, we wanted to use another OPC marker, Olig2. Since Olig2 is localized in the nucleus, we wanted a reporter of the Foxb1 lineage also localized in the nucleus. For this reason we used a different reporter, the ROSA26R mouse line (Soriano, 1999). In this line, Cre recombination causes expression of β-galactosidase which can be seen in the nucleus. We colocalized Olig2 and β-galactosidase on MO sections of heterozygotes and homozygotes (Figures 11A-F). Cell counting confirmed a significant increase of Olig2+ cells in the homozygotes ( Figure 11G). Additionally, we labeled dividing cells with BrdU (see ''Materials and Methods'' Section for details) and then labeled the tissues with BrdU and Olig2 (Figure 12). We found that, in homozygous mutants, more Olig2-expressing cells were dividing than in heterozygotes.

The G-Ratio Is Not Altered in the Foxb1-Deficient Hindbrain
Finally, we asked if there would be any obvious defect in myelination in the hindbrain of our mutants. The phenotype of Foxb1-deficient mice includes several behavioral and CNS developmental defects (Dou et al., 1997;Labosky et al., 1997;Alvarez-Bolado et al., 2000;Radyushkin et al., 2005; see ''Discussion'' Section). However, alterations suggesting myelination defects have not been described in these mice. This suggests that the OL in this mutant are able to myelinate correctly. To test this hypothesis, we measured axon and fiber diameter on electron microscopy images from the hindbrain of homo-and heterozygotes and found that the G-ratio    (Friede and Bischhausen, 1982) does not change in the mutants (Figure 13).

DISCUSSION
Lineage analysis of a mouse mutant line reveals transcription factor Foxb1 as a novel player in oligodendrocyte development, promoting neuron generation and OPC differentiation over OPC generation and proliferation. This novel function of Foxb1 is in line with the reported functions of the Fox superfamily of transcription factors, which regulate genetic cascades controlling proliferation, differentiation, metabolism, aging, survival and apoptosis (Carlsson and Mahlapuu, 2002). A case in point is the Foxo subfamily, consisting of negative regulators of genes crucial for cell cycle progression (Lam et al., 2013). Foxb1 is reportedly essential for the survival of a specific subpopulation of spinal motoneurons (Dou et al., 1997) and of a subset of hypothalamic cells (Alvarez-Bolado et al., 2000). However, a relation of Foxb1 with OL or the control of cell proliferation has not been described before.
In the Foxb1 null mutant mouse, the OL lineage increases to the detriment of the neuronal lineage. All neurons and macroglia share an early progenitor in the VZ of the embryonic neuroepithelium (Battiste et al., 2007;Pinto and Götz, 2007;Kriegstein and Alvarez-Buylla, 2009). Since part of the neuroepithelium belongs to the Foxb1 lineage (i.e., expresses Foxb1 or derives from Foxb1-expressing neural progenitor cells, NPCs), we have to assume that Foxb1-deficient NPCs are biased towards OPC generation. Therefore, a general function (direct or indirect) of Foxb1 would be to modulate a complex genetic cascade which has been given the name of neurogenesis/gliogenesis switch (Martynoga et al., 2012). In the cortex, the most extensively researched CNS region, neurogenesis requires Fox transcription factor genes like Foxc1 and Foxg1; reviewed in Martynoga et al. (2012). Foxb1, not expressed in the cortical VZ, could fulfill a similar role in other neuroepithelial regions.
Another consequence of Foxb1 deficiency is the predominance of OPC and immature OL over mature OL, indicating an additional function of Foxb1 inhibiting OPC proliferation and promoting their differentiation. Other members of the Forkhead gene family have roles in OL development. Foxj3 seems to have the opposite function to Foxb1, by stimulating OPC proliferation (Dugas et al., 2010). Foxa2 is essential for the induction and/or differentiation of OL in zebrafish (Norton et al., 2005) and Foxg1 inhibits the glial fate choice (including oligodendroglia; Brancaccio et al., 2010).
Our results suggest that Foxb1 would be one of many components in a cascade of genetic activation regulating a series of choices made by NPCs and the OPCs that derive from them. This function of Foxb1 would be exerted in the spatially restricted groups of NPCs expressing this gene, the ones giving rise to cell groups in the hindbrain and thalamus (and possibly also in the mammillary body (MBO) of the hypothalamus). Because other Fox genes are involved in similar functions in the cortex, we can assume that, to a degree, different restricted regions of neuroepithelium regulate the generation of the corresponding brain cells by using different members of the same gene families. Each of these members might perform a similar job but with some differences upon which the morphological and functional heterogeneity of CNS regions in the adult would ultimately be based.
Foxb1 is widely expressed in the neuroepithelium of the thalamus, hypothalamus, hindbrain and spinal cord (Alvarez-Bolado et al., 1999;Zhao et al., 2007Zhao et al., , 2008. Accordingly, we have observed clusters of Foxb1 lineage in thalamus, MBO (hypothalamus), pons and MO (we did not investigate the spinal cord) but not, for instance, in the cortex ( Figure 6A). Therefore, here we uncover specific, spatially restricted subpopulations of OPC and OL characterized by belonging to the Foxb1 lineage and whose proliferation is modulated by Foxb1. In the rodent CNS, OPC originate in discrete loci of the dorsal and ventral neuroepithelium (Woodruff et al., 2001;Rowitch, 2004;Kessaris et al., 2006;Rowitch and Kriegstein, 2010;Huang et al., 2013). Origin heterogeneity has some correlate in cellular properties like proliferation (Young et al., 2013) and marker expression (Butt et al., 1998b;Kleopa et al., 2004). Besides, different morphological classes of OL (Bjartmar et al., 1994;Butt et al., 1998a;Anderson et al., 1999) have been described, perhaps related to place of origin.
To address the question of the functional equivalence of OL of heterogeneous origins, we compared the main characteristics of lineage and phenotype between MO and thalamus. In both regions the Foxb1 lineage consists mostly of neurons and OL, together with some astrocytes. Interestingly, a robust portion of the thalamo-cortical bundle tract was labeled by our reporter (Figure 6A), indicating that a large number of thalamo-cortical projection neurons belong to the Foxb1 lineage. The Foxb1 null phenotype is similar in both regions: reduction of neurons, astrocytes and mature OL in favor of immature OL. In principle, this agrees with previous work indicating that OL from OPC originated in different CNS regions are not very different functionally (Kessaris et al., 2006;Psachoulia et al., 2009;Tripathi et al., 2011;Clarke et al., 2012; although white matter and gray matter OL are functionally different from each other; Viganò et al., 2013). But the two subpopulations that we have compared share Foxb1 lineage. Obviously OL from non-Foxb1-expressing regions will express different proliferation modulators. This implies that there must be a series of restricted neuroepithelial ''patches'' differentially expressing transcription factors which specifically modulate aspects of OL production.
Finally, a myelination phenotype could in principle be expected in the Foxb1 mouse mutants. However, neurological signs demyelination (like ataxia, unsteady gait, ocular paralysis, weakness and loss of sensation) have not been observed by us or other authors in these mutants. In addition, the G-ratio remained unchanged in the homozygous brainstem. We conclude that Foxb1 is not required for normal myelination.

CONCLUSION
Forkhead transcription factor Foxb1 is a novel modulator of neuronal and OL generation acting in certain restricted CNS regions. Foxb1 biases NPCs towards the neuronal and to a lesser degree the astrocytic lineages and inhibits the proliferation of OPC, favoring their differentiation. Foxb1-lineage OL are a novel subpopulation whose specific properties as well as their ability to replace other subpopulations (for instance, telencephalic OL) as part of a therapeutic approach are open questions.

AUTHOR CONTRIBUTIONS
YZ and EH performed experiments and analyzed results; TZ made the original observations and performed key preliminary experiments; XZ generated the Foxb1-Cre mutant line, assisted with the experiments and analyzed results; GA-B and XZ directed the project; YZ, EH and GA-B wrote the article; all authors revised the manuscript and approved the final version.