Abstract
Twenty years ago, the scientific community exhibited relatively little interest in the study of microglial cells. However, recent technical and conceptual advances in this field have greatly increased interest in the basic biology of these cells within various neurodegenerative diseases, including multiple sclerosis, Alzheimer’s disease, and traumatic brain/spinal cord injuries. The main functions of these cells in the normal central nervous system (CNS) remain poorly understood, despite considerable elucidation of their roles in pathological conditions. Microglia populate the brain before birth and remain in close lifelong contact with CNS-resident cells under the influence of the local microenvironment. Within the CNS parenchyma, microglia actively interact with two main cell types, astrocytes and neurons, which produce many factors that affect microglia phenotypes in the normal CNS and during neuroinflammation. These factors include interleukin (IL)-34, macrophage colony-stimulating factor, transforming growth factor-β, and IL-4, which promote microglial expansion, survival, and differentiation to an anti-inflammatory phenotype in the normal CNS. Under inflammatory conditions, however, astrocytes produce several pro-inflammatory factors that contribute to microglial activation. The interactions of microglia with neurons in the normal and diseased CNS are especially intriguing. Microglia are known to interact actively with neurons by facilitating axonal pruning during development, while neurons provide specific factors that alter microglial phenotypes and functions. This review focuses mainly on the roles of soluble neuronal factors that affect microglial phenotypes and functions and the possible involvement of these factors in the pathology of neurodegenerative diseases.
Introduction
Microglia are central nervous system (CNS)-resident myeloid cells that originate from common erythro-myeloid progenitors (EMPs), which themselves originate from embryonic stem cells (ESCs) in the yolk. Microglia populate the brain during early fetal development (; ). Later, microglia harbor the ability to self-renew locally and remain in the CNS microenvironment throughout life, where they comprise 10–15% of all cells in the brain and spinal cord. In this respect, microglia differ from resident macrophages in other tissues, which originate from hematopoietic stem cells (HSCs) (), although resident myeloid Langerhans cells in several tissues, such as the skin, represent a mixture of cells derived from ESCs and HSCs (). Under pathological conditions such as irradiation or inflammation, HSC-derived myeloid cells may also enter the CNS and acquire the characteristics of ESC-derived microglia, thus leading to a mixed population of HSC- and ESC-derived CNS-resident macrophages similar to that of dermal Langerhans cells ().
Currently, we understand that the phenotypes and functions of microglia are influenced strongly by the local CNS microenvironment. Even in a diseased CNS, microglia in unaffected areas exhibit a normal phenotype and are referred to as homeostatic microglia, whereas microglia proximal to the damaged area exhibit a distinct disease-associated phenotype (). Under normal conditions, homeostatic microglia are maintained at appropriate densities in various regions of the brain, mostly via local self-renewal (; ). During disease, microglia in damaged areas often exhibit heterogeneous and mixed-activation phenotypes and may play a beneficial or detrimental role, depending on the area, extent, and nature of neuronal damage and the stage of the disease (; ; ). Therefore, it is important to understand how the phenotypes and functions of microglia are determined by specific signals from other CNS-resident cells, such as astrocytes and neurons. This review discusses the nature of such signals and mechanisms of adaptation to the local microenvironment.
Epigenetic Changes Mediate Adaptation of the Microglia to Tissue-Specific Microenvironments
Modern studies have demonstrated that the adaptation of macrophages to local tissue microenvironments is mediated by epigenetic changes in chromatin (i.e., chromatin remodeling). This process enables the binding of several key transcription factors (TFs) that mediate microglial differentiation (; ). Like other tissue-resident macrophages, microglia reside in the CNS under the influence of tissue-derived factors that drive the expression of lineage-specific TFs such as PU.1 and CEBPα (). Both CEBPα and PU.1 are induced by macrophage colony-stimulating factor-1 (CSF-1) or its analog, interleukin (IL)-34 (), which are produced by astrocytes and neurons (; ). These factors drive the survival, renewal, and lineage-specific differentiation of microglia (). In addition to lineage-specific TFs, tissue-specific TFs complement and modulate the functions of core lineage-specific factors (; ), including SMAD family TFs driven by transforming growth factor (TGF) β, which is produced by astrocytes and neurons (). We found that mature microglia very strongly express TGFβ1 mRNA (unpublished observation), indicating that self-TGFβ1 could maintain SMAD2/3 expression in an autocrine manner. Several other factors, including but not limited to V-Maf musculoaponeurotic fibrosarcoma oncogene homolog B (MAFB), interferon response factor (IRF)8, Sal-like (SALL)1, and peroxisome proliferator-activated receptor (PPAR)γ, contribute to the transcriptional control of microglia identity in the normal CNS (, ; ). Under inflammatory conditions, other inducible TFs, such as nuclear factor (NF)κB, NF-of activated T cells (AT), and signal transducer and activator of transcription (STAT)1/3, contribute further to the phenotypes of activated microglia (). The cooperative binding of various lineage- and tissue-specific TFs, such as PU.1, CEBPα, IRF8, SMAD2/3, and SALL1, induce the modification of chromatin and generation of primed enhancers for gene expression, which is characterized by monomethylated H3K4 (H3K4me1). In the diseased CNS, inflammatory stimuli [e.g., IL-6, tumor necrosis factor (TNF)] induces the binding of additional factors, such as NFκB, NF-AT, and STAT1/3, and the acetylation of H3K27 (H3K27Ac) (). Thus, the actions of multiple TFs induce epigenetic changes that lead to the remodeling of chromatin and the formation of a specific mature microglial phenotype. The exact mechanism underlying this highly complex process remains elusive.
Epigenetic Changes in the Activation and Polarization of Macrophages and Microglia
The phenotypes and functions of immune cells such as microglia and macrophages depend on the type of activation. One example is the existence of pro-inflammatory M1-like macrophages, which are activated by interferon (IFN)γ and/or lipopolysaccharide (LPS), and M2-like macrophages, which are activated by IL-4 and/or IL-13 and associated with the resolution of inflammation and repair of damaged tissues (; ). The phenotypes of M1 and M2 macrophages are plastic, and the existing model of the activation and polarization spectrum oversimplifies the M1–M2 phenotypic dichotomy, especially in vivo (; ). Nevertheless, in vitro studies have clearly delineated a distinct pattern of specific TF expression in M1 macrophages, which is characterized by STAT1, STAT2, IRF4, and NFκB. In contrast, the M2 macrophage phenotype is mediated by STAT6, GATA3, and PPARγ (; ; ). Regarding specific markers, M1 macrophages express nitric oxide (NO) produced by the enzyme NOS2, high levels of major histocompatibility (MHC) class II and CD86 receptors, and the cytokines TNF and IL-6. In contrast, M2 macrophages express arginase (Arg1), extracellular matrix-binding lectin (Ym1/Chi3l3), and the chemokine CCL22, a heparin-binding protein (; ).
Histone methylation and acetylation are associated with both the M1 and M2 states of activated macrophages and microglia (; ). The methylation of H4R3 has been shown to positively regulate M2 by inducing the expression of the M2-associated TF PPARγ in mouse peritoneal macrophages (PMs) activated with IL-4 (). H3K4 methylation also positively regulates M2 polarization in human macrophages activated with M-CSF and IL-4 (). The enzyme JMJD3, known also as H3K27 demethylase, has been shown to be critical to the upregulation of IRF4 and Arg1 in mouse bone marrow-derived macrophages (BMDMs) stimulated with IL-4 (). The expression of JMJD3 is also upregulated in IL-4-treated mouse microglia, leading to H3K27 demethylation (). Moreover, the acetylation of H3K9 and H3K14 in the Tnf, Il6, Nos2, and H2Ab (MHC class II) promoter regions is a critical inducer of the expression of these M1-associated molecules in LPS-stimulated mouse microglia ().
Similar to other tissues, the CNS produces IL-4 via neurons and possibly astrocytes. This cytokine contributes to the expression of M2-like markers and may also induce the expression of the M2-associated TF PPARγ in mature microglia (, ; ). We found that normal microglia express Ym1 in a CNS-derived IL-4-dependent manner (). More recent studies based on single-cell RNA sequencing demonstrated that mouse microglia express Arg1, especially during the embryonic and early postnatal stages (). However, the initial concept of microglial polarization was criticized recently, as microglia were shown to express M1 and M2 markers simultaneously at the single-cell level (). We found this unsurprising, as we discovered long ago that microglia exhibited dual activation and an M1/M2 mixed phenotype in the context of experimental autoimmune encephalitis (). We believe that criticism of the concept of microglial polarization was mainly due to the misconception that microglia must exist in one of two mutually exclusive states (M1 or M2). More recent studies of macrophages and microglia demonstrated that these activation states are impermanent and somewhat dynamic. We also demonstrated that IL-4-activated macrophages exhibit a high level of plasticity, and that this is due to a high level of Egr2, which enables the cells to react to other activation stimuli (). Interestingly, mouse and human microglia express multiple early response genes, including Egr2, even at a single-cell level, which suggests a high level of cellular plasticity (). Importantly, therefore, microglia are exposed to a milieu of different cytokines (e.g., IL-4, TNF) during inflammation, and the state of activation represents a dynamic superposition of different activation pathways, rather than the mutual exclusion of the M1 and M2 states.
Role of Microrna in Microglial Phenotypes and Functions
In addition to histone methylation and acetylation, other epigenetic mechanisms regulate gene expression in microglia. One well-known mechanism involves the suppressive actions of regulatory microRNAs (miRNAs) against gene expression. MiRNAs are short (22–23 nucleotides) non-coding RNAs that bind complementarily to the mRNAs of target genes and either repress the translation or induce the degradation of these mRNAs (). In both cases, translation of the target gene and protein expression are decreased. The roles of miRNAs in microglial functions were reviewed recently (). Moreover, a recent study demonstrated the microglial–neuronal transfer of exosome-associated miRNAs. M1-activated microglia were shown to produce extracellular vesicles containing the microglia-specific miRNA miR-146a-5p, which is not detected in neurons. Upon transfer, this miRNA downregulated the expression of the genes encoding presynaptic synaptotagmin-1 and postsynaptic neuroligin-1 (). In this review, we focus on the roles of two neuronal miRNAs, miR-124 and miR-9, which are transferred from neurons to microglia and/or macrophages. Our screening of microRNAs that are expressed in microglia but not in resident PMs or BMDMs revealed the strong expression of miR-124 in the microglia (). Interestingly, miR-124 is expressed strongly in neurons and is responsible for the differentiation of neuronal progenitor cells (NPCs) into mature neurons (). We determined that miR-124 targeted CEBPα, a critical TF for macrophage and microglial differentiation. CEBPα was expressed in mouse embryonic (until E14) and early postnatal microglia (E15–P14) but not in mature microglia (P60), whereas miR-124 was expressed strongly in mature microglia, but not in embryonic and early postnatal microglia. The transfection of BMDMs with miR-124 decreased the expression of CEBPα and PU.1 and the pro-inflammatory cytokines TNF and IL-6, and increased the expression of the anti-inflammatory factors Arg1, Fizz1, and TGFβ1 (). Indeed, exposure to the pro-inflammatory stimuli TNF and IL-6 increased the expression and DNA binding of CEBPα and PU.1, which in turn increased the induction of downstream gene expression (). The upregulation of Arg1, Fizz1, and TGFβ1 in macrophages transfected with miR-124 was consistent with the phenotypes of M2-like macrophages activated with IL-4 or IL-13 (). Indeed, we found that IL-4 or IL-13 induced the expression of longer pre-miR-124 transcripts in BMDMs and lung resident macrophages in a STAT6-dependent manner, whereas this process was not observed in mature microglia from a normal CNS (). Therefore, the microglial expression of neuronal miR-124 was upregulated via mechanisms other than the intrinsic transcription of longer miR-124 precursors and subsequent processing and maturation into functional miR-124. Further experiments indicated the horizontal transfer of miR-124 and miR-9 from neurons to microglia (). Similar to miR-124, miR-9 is expressed strongly in neurons. This miRNA deactivates macrophages and microglia by targeting NFκB, the expression of which is induced in microglia by inflammatory stimuli (). Therefore, both miR-124 and miR-9 promote an anti-inflammatory phenotype in the normal CNS. These findings also indicate that normal neurons send continuous signals to microglia to maintain the latter cells in a quiescent state.
Horizontal Transfer of Mirna From Neurons to Microglia
Our understanding of the induction of miR-124 expression in mature microglia led us to hypothesize that this miRNA is transferred from mature neurons to microglia. Although previous reports described the transfer of miRNA between cell types (, ), most demonstrated the transfer of miRNAs via exosomes or microparticles (). We investigated in detail the presence of the neuronally abundant microRNAs, miR-124 and miR-9, in the extracellular space. Notably, both miR-124 and miR-9 were secreted actively by electrically active neurons, which was confirmed by using tetrodotoxin (TTX) to block secretion (). However, both miRNAs were secreted in various forms, including naked single-strand RNA (ssRNA), naked double-strand RNA (dsRNA), and ssRNA or dsRNA complexed with proteins, and within exosomes. Importantly, some proportion of miR-9 was co-localized with exosomes, whereas miR-124 was not associated with exosomes. Rather, miR-124 formed complexes with high-density lipoproteins (HDLs), which are produced in the CNS by astrocytes. These HDL–miR-124 complexes translocated efficiently into the cytoplasm of microglia and macrophages via scavenger receptors. This finding highlights an important mechanism by which functional neurons send continuous signals to the microglia to provide instruction and maintain a resting (non-activated) phenotype in the normal CNS (). We propose that neuronal electric and synaptic activity decreases, miR-124 and miR-9 secretions are blocked, and the microglial phenotype shifts from resting to activated during neurodegeneration.
Analogous Regulation of Gene Expression in Microglia and Neurons
We hypothesized that gene expression is regulated similarly, in neurons and microglia, as both cell types are closely associated with each other and exposed to the same microenvironment. Several findings support our hypothesis. First, we observed that microglia express neuronal miRNAs such as miR-124 and miR-9 (). Second, microglia produce neuronal trophic factors such as brain-derived neurotrophic factor (BDNF) (). Third, microglia express Egr1, c-Jun, and c-Fos, which are products of neuronal early response genes (). Fourth, microglia express Sall1, which, together with Egr1, is associated with neuronal maturation and synaptic pruning (). Egr1, c-Jun, and c-Fos are hallmarks of neuronal synaptic activity (), while Egr2 is involved in macrophage activation, polarization, and plasticity (). However, c-Fos forms complexes with c-Jun to form activator protein-1 (AP-1), a very potent TF associated with macrophage activation (). AP-1 induces the expression of pro-inflammatory genes in macrophages and microglia (; ). Alone, c-Fos suppresses the expression of M1-associated genes such as Nos2, Tnf, and Il6 (; ). CEBPβ is another interesting TF that is regulated in macrophages by Egr1–3 and the cAMP pathway (, ). CEBPβ is important for cortical neurogenesis and may thus induce the expression of both myeloid and neuronal genes (). Sall1 also regulates cortical neurogenesis () and serves as a unique marker of microglia. The miRNA miR-124 inactivates the transcriptional repressor REST, which in turn inhibits the expression of neuronal genes in non-neuronal cell types (). Mir-124 is expressed in microglia and M2 macrophages. Sall1-deficient or miR-124 inhibitor-treated microglia lose their processes that are typical for adult microglia in normal CNS (ramified form) and take a more activated amoeboid form, indicating that the resting microglial phenotype might be maintained by neuronal genes (; , ). In other words, neurons and mature microglia share similar expression patterns for several genes. We believe that these neuronal genes may contribute to the unique phenotypes of microglia in the CNS. However, the induction of neuronal gene expression in microglia remains unclear and must be addressed. We propose that neuronal gene expression in microglia is associated with similar epigenetic changes that occur in both cell types during development. During neural lineage commitment, H3K27 in the promoter regions of many neural lineage genes is demethylated by the enzyme JMJD3 (), similar to the effects of IL-4 on mouse BMDMs. Simultaneously, H3K27 is methylated in non-neuronal cells (including non-activated peripheral macrophages) (). These findings indicate similar epigenetic changes in microglia, M2 macrophages, and neuronal cells.
Besides the demethylation of H3K27 in M2 macrophages, miR-124 is upregulated by the IL-4 and cAMP pathways in mouse BMDM (), while microglia receive horizontal transfers of miR-124 and miR-9 from neurons (). Therefore, we propose that neuronal miR-124 and miR-9 inhibit REST in microglia, leading to the expression of several neuronal genes, similar to the consequences of miR-124 and miR-9 overexpression in fibroblasts (). As the deactivation of REST and upregulation of miR-124 were shown to be associated with the modification of the neuronal BAF chromatin remodeling complex during neuronal lineage commitment (), we hypothesized that BAF would also be modified in the microglia, compared with non-activated BMDM. To test this hypothesis, we investigated the neuronal BAF chromatin remodeling complex (), which regulates the expression of neuronal genes during differentiation from embryonic stem cells (ESCs) to neuronal progenitor cells (NPCs) from NPCs to mature neurons (), in neurons, peritoneal macrophages (PMs), BMDMs, and microglia (Figure 1A). In the ESC stage, the esBAF complex exists, and the co-factors BAF53A and SMARCC1 are expressed predominantly. In the NPC stage, the npBAF complex retains BAF53A but includes two new factors, BAF45A and SMARCC2. Finally, in mature neurons, the nBAF complex comprises BAF45B and BAF53B. The expression of the neuronal genes BEX, SYT1, MAP2, and TUBB3 increased gradually during the ESC→ NPC→neuron transition path (Figure 1A). We similarly compared the expression levels of transcripts encoding factors in the esBAF, npBAF, and nBAF complexes in mature microglia, BMDMs, PMs, and cultured mature cortical neurons, as described in our earlier studies (, ; , ). We observed a similar expression of BAF53A and SMARCC1, which encode esBAF components, between microglia and neurons and between microglia and BMDMs. However, these genes were expressed at significantly higher levels in microglia than in PMs (Figures 1B,E). We observed a similar pattern in the expression of BAF45A and SMARCC2, which encode npBAF components. These genes were expressed similarly in microglia and neurons, at similar or slightly higher levels in microglia relative to BMDMs, and at significantly higher levels in microglia than in PMs (Figures 1C,F). However, BAF53B and BAF45B, which encode nBAF components, were only expressed at detectable levels in neurons and microglia, but not BMDMs and PMs (Figures 1D,G). The neuronal genes BEX, SYT1, and MAP2 were expressed in neurons and microglia, but not in BMDMs and PMs (Figure 1H). TUBB3, the most abundant neuronal gene, was not expressed in microglia, indicating that the previous results could not be attributed to the contamination of microglia preparations with neuronal cells (Figure 1H, TUBB3). Therefore, in contrast with other macrophages, microglia express factors associated with the nBAF complex, as well as several neuronal genes. Although the roles of neuronal gene products such as MAP2 in the microglial phenotype remain unclear, we propose that these factors contribute to the unique phenotype of mature microglia in the normal CNS.
FIGURE 1
Roles of Neuronal Soluble Factors in the Maintenance of the Microglial Phenotype
Following our discovery of the horizontal transfer of neuronal miR-9 and miR-124 from electrically active neurons to microglia, we hypothesized that the microglial phenotype is influenced strongly by soluble neuronal factors (Table 1 and Figure 2). Accordingly, these soluble neuronal factors exhibit great potential for future therapeutic interventions targeting neurodegenerative diseases. Both astrocytes and neurons can produce IL-4, TGFβ1, and IL-34, which greatly affect the microglial phenotype, as discussed previously (Table 1). Neuronal IL-4 might further contribute to H3K27 demethylation in microglia (). Neurons also produce the chemokines CCL2, CCL12, and CX3CL1 (both membrane-bound and soluble forms), which can induce microglial migration toward neurons (CCL2 and CCL12) and microglial deactivation (CX3CL1) (). Neuronal growth factor (NGF) and BDNF also contribute to the anti-inflammatory microglial phenotype (Table 1; ; ). Neurotransmitters are other important molecules released by electrically active neurons that can directly affect microglia. Common neurotransmitters, such as serotonin, dopamine, and GABA, deactivate microglia, while glutamate activates these cells (Table 1; ). ATP is released by activated and damaged neurons and contributes to microglial activation and inflammation (). The neuronal microRNAs miR-124 and miR-9 are transferred to the microglial cytoplasm, where they downregulate the expression of CEBPα and NFκB and deactivate the cells (Table 1; ). Finally, the complement components C1q and C3 mediate neuronal axonal pruning by microglia via complement receptors (Table 1). Interestingly, C1q expression is induced in neurons via a TGFβ1-mediated mechanism, while C3 is present in neuronal synapses (). In summary, many factors, including pro- and anti-inflammatory stimuli, affect communication between neurons and microglia. The balance of these stimuli determines the ultimate phenotype of microglia in the normal or diseased CNS (Figure 2).
TABLE 1
| Class of mediators | Neuron-derived mediators | Changes during neuroinflammation/neurodegeneration | Effect on microglia |
| Cytokines | IL-4 | Decreased | Promote anti-inflammatory phenotype and expression of: Ym1, Fizz1, TGFβ1 (, ; ; ) |
| TGFβ1 | Decreased | Promote homeostatic phenotype of microglia in normal adult CNS () | |
| IL-34 | Increased | Homeostatic maintenance, proliferation, and survival of microglia (; ; ) | |
| Chemokines | CCL2 | Increased | Microglia migration, activation, and proliferation () |
| CXCL12 | Increased | Microglia migration and activation () | |
| CX3CL1 (soluble form) | Decreased | Deactivate microglia () | |
| Growth Factors | NGF | Increased | Promote anti-inflammatory phenotype of microglia () |
| BDNF | Increased | Suppress release of NO in microglia. Promote anti-inflammatory phenotype () | |
| Neurotransmitters | Serotonin (5HT) | Decreased during TBI-induced neuroinflammation | Decreased IFNγ-induced activation of macrophages and possibly microglia () |
| Dopamine | Decreased | Possibly suppress microglia activation via DR2 () | |
| Glutamate | Decreased | Promote microglia activation and expression of TNF and NO () | |
| GABA | Decreased | Inhibit microglia activation and release LPS-induced TNF and IL-6 () | |
| Low-molecular-weight mediators | ATP | Increased | Activate microglia () |
| microRNAs | miR-124 miR-9 | Decreased Decreased | Deactivate microglia () |
| Complement | C3 | Increased | Mediate synaptic pruning by microglia () |
| C1q | Increased |
Neuron-derived soluble factors that affect the activation state of microglia in normal CNS and during neuroinflammation and neurodegeneration.
FIGURE 2
Concluding Remarks
Microglia represent a unique population of resident myeloid cells in the CNS. The phenotypes of these cells are influenced strongly by the local microenvironment and determined by the specific regulation of gene expression at the epigenetic level. Currently, neuronal cells are thought to actively influence the phenotypes of microglia. In the normal CNS, electrically and synaptically active neurons maintain microglia in a deactivated state, whereas changes in the balance of inhibitory vs. activating stimuli in the contexts of neuroinflammatory and neurodegenerative diseases cause immediate changes in the microglial phenotype and induce activation. A further understanding of the interactions of neurons and microglia in the normal CNS would ultimately lead to the discovery of new pathways. This information would suggest potential mechanisms by which homeostasis could be restored in pathological settings, as well as potential treatment options for neurodegenerative diseases such as multiple sclerosis, Alzheimer’s disease, and Parkinson’s disease.
Statements
Author contributions
TV and EP conceived the review and study. TV, AY, and MD performed the experiments. TV, TS, and EP analyzed the data. TS and EP prepared the manuscript.
Funding
This work was supported by Research Grant Council–General Research Fund, reference no. 14113316 (Hong Kong Government, Hong Kong), and by Research Grant Council–Areas of Excellence Fund grant (Hong Kong Government, Hong Kong), reference no. AoE/M-604/16.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as constituting a potential conflict of interest.
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Summary
Keywords
microglia, neurons, neuroinflammation, transcriptional regulation, microRNA
Citation
Veremeyko T, Yung AWY, Dukhinova M, Strekalova T and Ponomarev ED (2019) The Role of Neuronal Factors in the Epigenetic Reprogramming of Microglia in the Normal and Diseased Central Nervous System. Front. Cell. Neurosci. 13:453. doi: 10.3389/fncel.2019.00453
Received
14 June 2019
Accepted
23 September 2019
Published
11 October 2019
Volume
13 - 2019
Edited by
Xuping Li, Houston Methodist Research Institute, United States
Reviewed by
Maria Angeles Arevalo, Spanish National Research Council (CSIC), Spain; Gyun Jee Song, Catholic Kwandong University, South Korea
Updates
Copyright
© 2019 Veremeyko, Yung, Dukhinova, Strekalova and Ponomarev.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Eugene D. Ponomarev, eponomarev@cuhk.edu.hk; eugpon@gmail.com
This article was submitted to Non-neuronal Cells, a section of the journal Frontiers in Cellular Neuroscience
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