Department of Anatomy, Keio University School of Medicine, Tokyo, Japan
The central nervous system (CNS) and the immune system are both intricate and highly organized systems that regulate the entire body, with both sharing certain common features in developmental mechanisms and operational modes. It is known that innate immunity-related molecules, such as cytokines, toll-like receptors, the complement family, and acquired immunity-related molecules, such as the major histocompatibility complex and antibody receptors, are also expressed in the brain and play important roles in brain development. Moreover, although the brain has previously been regarded as an immune-privileged site, it is known to contain lymphatic vessels. Not only microglia but also lymphocytes regulate cognition and play a vital role in the formation of neuronal circuits. This review provides an overview of the function of immune cells and immune molecules in the CNS, with particular emphasis on their effect on neural developmental processes.
The central nervous system (CNS) and the immune system have much in common. The most prominent characteristic of either system is their ability to transmit information to distant parts of the body with extraordinary specificity and diversity. In the immune system, the diversity of acquired immune cells–T cells and B cells–is generated by the stochastic VDJ recombination of T cell receptors (TCRs) and immunoglobulin (Ig) genes, and somatic hypermutation of TCRs (at least in the shark) (Ott et al., 2018) and immunoglobulins. For example, the human heavy chain region contains 38–46 variable (V) gene segments, 23 diversity (D) gene segments, and 6 joining (J) gene segments, and one segment of each type is selected in each lymphocyte by a mechanism called VDJ recombination. Moreover, the many different combinations of heavy- and light-chain variable regions that pair to form the antigen-binding site result in at least 1011 different receptors. The diversity of immunoglobulins is magnified by somatic hypermutation that occurs after the initiation of immune response and introduces point mutations into the rearranged variable region to enhance the reactivity to antigen. As for T cells, theoretically, 1015 TCRs can be produced by using almost the same mechanism as for immunoglobulins. This mechanism is critical for the evolution of the vertebrate adaptive immune system, because the genome with its limited size (approximately 3 billion nucleotides) could not directly encode all the possible antigen receptors. On the other hand, the human brain contains approximately 1011 neural cells that are classified into hundreds of different neuronal subtypes based on cell morphology, gene expression profile, and axon/dendrite projection patterns. For example, 21 neuronal subtypes are identified in the human frontal cortex by single-cell methylomes (Luo et al., 2017). Each neuron collects inputs from and sends outputs to many other specific neurons–on average, 103 for both inputs and outputs for a mammalian neuron. In addition, glial cells, which outnumber neurons approximately 10 times, cover synapses and control the neural network. It is known that each human astrocyte can contact and encompass nearly 2 × 106 synapses (Oberheim et al., 2006). In this way, specific and diverse neural networks are established, although the precise underlying molecular mechanisms have not been completely illustrated. During the generation of diversity, some non-functional or autoreactive TCR-expressing T cells and undesirable neurons could emerge. These T cells undergo apoptosis in the thymus by a mechanism known as positive and negative selection, and some neurons are removed by apoptosis or lose their synaptic connections through synaptic pruning. Moreover, both systems possess memory mechanisms. In the immune system, after invasion of bacteria, viruses, and other disease-causing organisms, the appropriate acquired immune cells that can respond to specific antigens are expanded and stored as memory T and B cells, so they can immediately generate an accelerated and more robust antibody-mediated immune response when the pathogen is encountered again. On the other hand, synaptic plasticity, including long-term potentiation (LTP) and long-term depression (LTD), underlie memory in the nervous system. In addition, both systems use the mechanisms of accelerators and brakes. In the immune system, there are immunosuppressive T/B cells (Treg, Breg) (Sakaguchi et al., 2008; Rosser and Mauri, 2015) and their imbalance results in allergy and autoimmunity. On the other hand, CNS neurons are classified into excitatory and inhibitory neurons, and the appropriate balance between these two populations is critical for neuronal networks to function normally (Yizhar et al., 2011). During the formation of neural circuits, both excitatory neurons and inhibitory interneurons undergo extensive cell death in the critical window of postnatal development (Southwell et al., 2012) and the survival of interneurons depends on the activity of excitatory pyramidal neurons (Wong et al., 2018). Of note, acquired immune system cells and highly developed myelination in the nervous system appeared at nearly the same time during evolution, around the evolution from jawless to cartilaginous fish (Zalc et al., 2008). It would be interesting if this was not mere coincidence but the two phenomena were causally linked. In addition, our understanding of the CNS has recently dramatically changed from an “immune privileged site” to a “special immune-controlled site.” In 2015, it was discovered that functional lymphatic vessels line the dural sinuses, and are able to carry both fluid and immune cells from the cerebrospinal fluid to the deep cervical lymph nodes (Louveau et al., 2015). The importance of meningeal lymphatic vessels for waste clearance was confirmed because impairment of meningeal lymphatic function caused cognitive impairment in mice (Da Mesquita et al., 2018). These discoveries shed more light on the interaction between the CNS and the immune system. Moreover, emerging evidence suggests that an increasing number of molecules that are typically associated with the immune system are also expressed in various CNS regions and play crucial roles in brain development. This review summarizes the reports on the function of immune cells (Figure 1) and immune molecules (Table 1) mainly in CNS development during the embryonic and early postnatal periods, with some attention paid to their function in more mature brains.
Contribution of Immune Cells to CNS Function
In the steady state, many lymphocytes reside mostly in the meninges and choroid plexus; however, a few lymphocytes are also found in the brain parenchyma, such as in the fimbria of the dorsal hippocampus and anterior olfactory nucleus, as clearly illustrated by reconstitution of green fluorescent protein-expressing lymphoid cells in Rag2–/– mice (Song et al., 2016). The most dominant immune cells in the brain are microglia, which comprise 80% of brain immune cells. Other immune cells identified in the brain include myeloid cells, monocytes/macrophages, dendritic cells, T cells, B cells and natural killer (NK) cells (Korin et al., 2017). Lymphocytes (including T cells, B cells, and NK cells), which are identified as a CD45hi population, are scarce in the CNS, with approximately 10,000 per hemisphere in adult naïve mice (Pösel et al., 2016). However, it is now clear that these limited numbers of immune cells have a significant impact on brain function. In particular, T cells have been implicated in complex brain processes including spatial learning, memory, emotional behavior, and stress responsiveness. For example, in mice undergoing the Morris-water-maze test (MWM), CD4+ T cells (helper T cells), but not CD8+ T cells (cytotoxic T cells), are recruited to the meninges, and secrete interleukin (IL)-4. IL-4 skews macrophages and microglia to an M2 (anti-inflammatory) phenotype, and induces the production of brain-derived neurotrophic factor by astrocytes, leading to the improvement of spatial learning and memory (Kipnis et al., 2004; Ziv et al., 2006; Wolf et al., 2009; Derecki et al., 2010; Radjavi et al., 2014). Previous studies have also demonstrated that B cells are not required for these processes because B cell-deficient μMT mice do not exhibit learning disabilities (Wolf et al., 2009; Radjavi et al., 2014).
In contrast to the adult brain, data regarding the interaction of immune cells and neural cells— except for microglia—during developmental stages are quite limited. However, epidemiological studies have demonstrated a link between maternal infection and the onset of neurodevelopmental disorders, such as autism spectrum disorder (ASD), schizophrenia, epilepsy, cerebral palsy, anxiety, and major depressive disorder, pointing to the association between the immune system and neural development (reviewed in Knuesel et al., 2014; Estes and McAllister, 2016). Animal models using rodent and non-human primates have also clearly demonstrated a causal relationship between maternal infection and ASD- and schizophrenia-related behavioral abnormalities. It is widely accepted that a major consequence of maternal immune activation (MIA) are changes in microglial morphology, distribution, and the expression level of several marker proteins. Moreover, it is known that microglia have multifaceted functions during normal brain development. It has recently been reported that acquired immune cells are also engaged in the developmental processes of the CNS.
Neonatal Immune Cell Population
Analyses of embryonic and neonatal immune populations in the CNS remain limited; however, one report illustrated that a small number of lymphocytes infiltrated the developing mouse brain even at embryonic day 16 (E16) and, among the investigated cell types, including CD4+ T cells, CD8+ T cells, and B cells, B cells are the most abundant in the CNS, peaking at approximately 5% of total lymphocytes (Tanabe and Yamashita, 2018b). Another study, using CD11c/EYFP transgenic mice, clearly illustrated that CD11c+ (also known as integrin αX and complement component 3 receptor 4 subunit) cells—which include monocytes, macrophages, dendritic cells, granulocytes, and NK cells—were present along the ventricles and within the adjacent parenchyma at E16 and postnatal day 2 (Bulloch et al., 2008). However, there have been no detailed reports describing the subpopulation of immune cells in the developing brain.
Microglial Function in CNS Development
Microglia are tissue-resident macrophages that play essential roles in innate immunity and have an origin that is different from other immune cells. Hoxb8-negative microglia arise from erythromyeloid precursors in the yolk sack during primitive hematopoiesis and infiltrate the brain at E9.5 in mice (Ginhoux et al., 2010), immediately after the onset of angiogenesis and neurogenesis. In contrast, Hoxb8-positive microglia infiltrate the brain at E12.5 (De et al., 2018). Although microglia are initially located along the meninges and ventricles, after E14 they distribute broadly throughout the cortex and then change their distribution to avoid the cortical plate. After E18, they again enter the cortical plate and begin to distribute to the entire cortex and increase their numbers dramatically (Reemst et al., 2016). During these dynamic changes in microglial distribution, the neural system undertakes highly orchestrated processes, including angiogenesis/vascularization, proliferation and migration of neurons and glia, programed cell death of neural stem cells and neurons, formation of synapses, myelination and establishment of neuronal circuits. Microglia contribute virtually to all of these events (reviewed in Kettenmann et al., 2013; Wu et al., 2015). For example, microglia regulate angiogenesis/vascularization by clearing excess vessels and participating in vessel anastomosis (Fantin et al., 2010), control the number of neural stem cells by phagocytosis (Cunningham et al., 2013), and regulate the survival of neurons in layer 5 via insulin-like growth factor 1 secretion (Ueno et al., 2013). They also modulate major events in forebrain wiring. These include the regulation of invasion of tyrosine hydroxylase-positive dopaminergic interneurons into the subpallium, the laminar positioning of parvalbumin-positive cortical interneurons (Squarzoni et al., 2014), and the control of axon projection through the corpus callosum (Pont-Lezica et al., 2014). Moreover, microglia regulate synaptic formation and synaptic pruning (through activation of the classical complement cascade) (Stevens et al., 2007; Miyamoto et al., 2016); they also regulate myelination by promoting the survival and differentiation of oligodendrocyte precursor cells (OPCs) and the maturation of oligodendrocytes (Pang et al., 2013; Shigemoto-Mogami et al., 2014).
Role of T Cells During CNS Development
In contrast to the contribution of T cells in adult brain function, very little is known about their function during embryonic and neonatal stages. One of the few explored contributions is their involvement in the pathophysiology of neonatal brain injury. Using postmortem brains from human preterm infants with periventricular leukomalacia, and animal models of preterm brain injury and sepsis-induced white matter brain injury, it was shown that γδ T cells—which have a distinctive TCR and have features of non-MHC-restricted antigen recognition and abundant cytokine secretion capacity—were responsible for injury in the developing brain, and that depletion of γδ T cells resulted in protection from injury (Zhang et al., 2017; Albertsson et al., 2018; Nazmi et al., 2018). Moreover, other groups have also demonstrated that T-helper 17 (Th17) lymphocytes coordinate neuroinflammatory responses in lipopolysaccharide (LPS)-sensitized hypoxic-ischemic injury in neonates (Yang et al., 2014). It has been also reported that TCRβ –/–γ–/– mice, which lack both αβ T cells and γδ T cells, exhibit altered size of several areas of the brain and lose sex differences (Rilett et al., 2015). Our knowledge of T cell involvement in CNS development is still fragmented and more work on T cell function in normal CNS development is needed.
B Cells in Oligodendrogenesis
As mentioned above, B cells accumulate in the neonatal brain and decline in number with age. Most of these B cells are IgMhi B-1a cells (Tanabe and Yamashita, 2018b), which have innate-like characteristics and participate in maintaining tissue homeostasis (Baumgarth, 2011). These B-1a cells are suggested to be mature and are recruited to the meningeal space and lateral ventricle depending on the chemokine receptor CXCR5 and in response to CXCL13 secreted from the choroid plexus. B-1a cells secrete natural IgM antibody and promote the proliferation of OPCs through the Fc receptor for IgM (Fcα/μR). Antibody depletion of B-1a cells diminishes the number of oligodendrocytes and results in reduction of myelinated axons in neonatal mouse brains (Tanabe and Yamashita, 2018b). However, depletion of B-1a cells by antibody treatment also resulted in a decrease in the number of microglia in the subventricular zone. Therefore, it has not yet been completely ruled out that B-1a cells may also affect oligodendrogenesis indirectly through microglia. More detail is provided in Tanabe and Yamashita (2018a, b).
Molecules That Play Important Roles in Both the Nervous System and the Immune System
It is known that these two systems share molecular mediators of communication in establishing the ability to monitor and respond to changes in the internal milieu and outside environment. Some of these are discussed in this section.
MHC Class I
MHC class I (MHCI) genes, known to be important for antigen presentation, are polygenic and polymorphic genes, comprising three classes (H2-K, -D, and -L) and multiple variants in mice. They were shown to be expressed in neurons at axons, dendrites and synapses, and in glial cells, especially highly during early postnatal stages. The function of MHCI is well reviewed in Elmer and McAllister (2012) and McAllister (2014). In brief, they are engaged in activity-dependent refinement and plasticity in the visual system, and regulate synaptic plasticity and motor learning in the cerebellum. An important question in this field is whether the diversity of MHCI is necessary for these functions. Synapse elimination and eye-specific axonal segregation in the lateral geniculate nucleus (LGN) were impaired in mice deficient in H2-Kb and H2-Db (KbDb–/–), and were rescued by expressing a single MHCI molecule H2-Db in neurons (Lee et al., 2014). However, whether each MHCI has specific functions and whether its polymorphism is related to CNS development and cognitive function related to diseases such as autism and schizophrenia remain to be elucidated.
The other major question concerns the MHCI signaling pathway. The TCR is the most widely known receptor for MHCI; however, no TCR protein has been detected in the CNS (Syken and Shatz, 2003). In contrast, CD3ζ, a component of the TCR, is expressed in the LGN during development (described below). Moreover, messenger RNA for PirB (paired Ig-like receptor B), an innate Ig-like transmembrane receptor for MHCI that antagonizes the integrin and MAP kinase signaling cascades (Takai, 2005), is highly expressed in neurons of the cerebral cortex, olfactory bulb, and granule cells of the cerebellum (Syken et al., 2006). Of note, mice deficient for CD3ζ (Huh et al., 2000) or PirB (Syken et al., 2006) also exhibit defects in the activity-dependent refinement of connections, similar to β2m–/–TAP1–/– and KbDb–/– mice. Other immune receptors, such as KIR (killer cell immunoglobulin-like receptor) (Bryceson et al., 2005) and Ly49 (a member of the NK family of innate immune receptors) (Zohar et al., 2008), are also believed to be potential neuronal receptors for MHCI. Moreover, whether MHCI molecules in the CNS really present antigens, and if so, what kinds of antigens are presented and whether they are essential for establishing specific neural networks remains to be answered.
The Complement Family
The classical complement family, an immune pathway that functions to eliminate pathogens and apoptotic cells, also plays an important role in synaptic remodeling. Its function has been reviewed several times, such as in Veerhuis et al. (2011) and Stephan et al. (2012). In brief, complement is produced by neurons and glial cells, especially by microglia and astrocytes, from early developmental periods to adulthood. Complement receptors CR3 (also known as CD11b/CD18, Mac-1, and integrin αMβ2) and CR5 are expressed in resident microglia. These complement proteins are engaged in synaptic refinement of retinal ganglion cell (RGC) projections to the dorsal LGN of the visual thalamus and they are also implicated in neurogenesis, migration, and neuronal survival during development and adulthood. The complement family play these important functions by cooperating with other proteins, because C1q co-localizes with H2-D and H2-K at synapses (Datwani et al., 2009), and the antibody and pentraxin families are involved in the complement cascade, as discussed below. C1q homologous proteins, including C1ql2 and Cbln1, are also engaged in synaptic formation, as reviewed in Südhof (2017) and Yuzaki (2017). However, much remains to be resolved: What signals control the activation of the complement cascade? Are they used similarly during development and adulthood? What are the critical molecules for synaptic pruning that might be the potential pharmacological targets of developmental and neurodegenerative diseases and injuries?
The blood-brain barrier prevents large molecules, such as antibodies, from entering the brain parenchyma. However, FcγRIIB, a low-affinity membrane receptor for IgG, which negatively regulates B cell receptor-induced signaling, is expressed in Purkinje cells and Bergmann glia in the developing cerebellum. In addition to FcγR, Fcα/μR, a receptor for the Fc region of IgA and IgM, is expressed in OPCs (Nakahara et al., 2003a, b; Tanabe and Yamashita, 2018b). Although the function of these Fc receptors is not yet fully understood, IgG was reportedly detected in the developing rat cortex, and immunohistochemical signals were observed in subplate and other early-generated cortical neurons as well as in retinal and cerebellar neurons during early developmental stages (Upender et al., 1997). The origin of these IgG proteins remains unclear. Because IgG is actively transferred from the mother to the fetus across the placenta using neonatal Fc receptors, and the barrier function of the blood-brain barrier is not complete until E15, maternal antibodies may leak into the fetal brain through blood vessels.
CD3 is the most commonly used T cell marker and is composed of four subunits: CD3δ, CD3ε, CD3γ, and CD3ζ. They assemble to form three types of dimers (δε, γε, ζζ), and serve as a co-receptor for MHC-TCR signaling (Call and Wucherpfennig, 2007). CD3ζ is expressed by retinal neurons located in the RGC layer in the developing retina and is localized at synapses in the inner plexiform layer during the period of synapse formation. CD3ζ participates in the eye-specific segregation of RGC axon projections to the dorsal LGN (Huh et al., 2000) and glutamate receptor (GluR)-mediated synaptic activity-dependent synapse formation of RGCs in the retina and dorsal LGN (Xu et al., 2010). CD3ζ is also expressed by hippocampal neurons and the deficiency of CD3ζ results in enhanced LTP and lack of LTD. CD3ζ activation on hippocampal neurons affects cell morphology by promoting dendritic pruning (Huh et al., 2000; Barco et al., 2005; Baudouin et al., 2008). CD3ε is expressed with FcγR II B on Purkinje cells and Bergmann glia in the cerebellar cortex during development, and both CD3ε-deficient mice and FcγR II B-deficient mice exhibit impaired development of Purkinje cells, enhanced paired-pulse facilitation of parallel fiber-Purkinje cell synapses, and poor rotarod performance at high speed (Nakamura et al., 2007). The precise function of these molecules is summarized in a table in Elmer and McAllister (2012). However, the neuron-specific signaling cascade through CD3 and FcγR II B is yet to be uncovered.
Cytokines are small signaling proteins secreted mostly by immune cells that regulate diverse immunological responses. However, many, such as IL-1α, IL-1β, IL-4, IL-6, IL-10, IL-11, IL-13, IL-18, IL-33, TNF-α, TGF-β and IFN-γ are also expressed in the CNS and are involved in cell survival, proliferation and differentiation, axonal growth and synaptogenesis, as reviewed in Bauer et al. (2007). For example, maternal IL-6 is the central molecule that alters social and cognitive behaviors of the offspring of immune-activated mothers (Smith et al., 2007; Wu et al., 2017), and working memory performance of 2-year-old children can be predicted by measuring maternal IL-6 (Rudolph et al., 2018). It is important to take into consideration that both mother and fetus can produce cytokines, and maternal peripheral and placental cytokines can also reach the fetal brain to directly affect CNS development. If pregnant mice colonized with commensal segmented filamentous bacteria undergo immune activation by infection, high amounts of IL-17a is produced by the mother’s intestinal Th17 cells, is transferred to the fetal brain and binds to IL-17R expressed on neurons, resulting in behavioral and cortical abnormalities that resemble those observed in autism (Choi et al., 2016; Kim et al., 2017; Shin Yim et al., 2017). Moreover, astrocyte-derived IL-33, which is one of the alarmins released by tissue damage, is used for promoting synapse refinement during development (Vainchtein et al., 2018).
Chemokines are chemotactic cytokines, which direct cell migration, and were originally identified as potent attractants for leukocytes to mediate acute and chronic inflammation. However, accumulating evidence suggests that they also play an essential role in mediating neuron-microglia crosstalk in the developing and mature brains, as illustrated in Ransohoff (2009) and Williams et al. (2014).
One of the most recognized examples is the CX3CL1 (also known as fractalkine) signaling pathway (Paolicelli et al., 2014). Briefly, neuron-derived CX3CL1 and its receptor CX3CR1, which is expressed mostly on microglia, promote microglial recruitment to neuronal circuits by increasing their process movement and cellular migration. This signaling also influences the survival of developing neurons, pruning of synapses, synaptic transmission, synaptic plasticity and connectivity, affecting learning, memory, and behaviors. CXCL12 (also known as stromal cell-derived factor-1, SDF-1)-CXCR4 signaling is also required for the appropriate migration of microglia, neural progenitor cells (NPCs), cortical interneurons, and Cajal Retzius cells. It also controls neurogenesis, axon guidance/pathfinding, neurite outgrowth and maintenance of NPCs, as reviewed in Li and Ransohoff (2008), Zhu and Murakami (2012), and Guyon (2014).
Toll-like receptors (TLRs) are pattern recognition receptors involved in the induction of the innate immune response. There are 13 TLRs identified in mice. Among them, TLR 2, 3, 4, 8, and 9 are expressed in the CNS, and their contribution to various phenomena is suggested, including neurite outgrowth, NPC proliferation, structural plasticity, cognition, anxiety, sensory, and motor behaviors, as discussed in Kioussis and Pachnis (2009), Okun et al. (2011), and Khariv et al. (2013). For example, TLR3 is highly expressed during early developmental stages, its activation reduces embryonic NPC proliferation in the subventricular zone and adult NPC proliferation in the dentate gyrus, and it inhibits neural outgrowth. TLR3 signaling has great impact on cognition; TLR3 deficiency causes improved spatial working memory and contextual fear memory, impaired amygdala-dependent cued fear memory and anxiety. However, the endogenous ligands that activate TLRs under physiological conditions, and whether they affect the development of neural circuits and/or cause more acute effects on synaptic plasticity remain unknown.
The pentraxins (PTX) are an evolutionarily conserved family of proteins characterized by a pentraxin protein domain. Some of them, such as C-reactive protein (CRP) and PTX3, are involved in acute immunological responses. It is well known that CRP is a binding partner of C1q and may be involved in synaptic pruning through C1q, and PTX3 can modulate phagocytic activity of microglia and promote functional synapse formation (Jeon et al., 2010; Fossati et al., 2019). Moreover, neural pentraxin 1 (NPTX1) and 2 (NPTX2) mediate synaptic refinement in the developing visual system (Bjartmar et al., 2006) and NPTX2 and neuronal pentraxin receptor (NPTXR) are required for GluA4 expression within parvalbumin-positive fast-spiking interneurons. In Nptx2–/–Nptxr–/– mice, GluA4 is markedly reduced, with consequent reductions in AMPA receptor function in the parvalbumin-positive interneurons, which compromise circuit recruitment of these interneurons, leading to deficits in network rhythmogenesis and behavior (Pelkey et al., 2015).
Function of Major Neuronal Molecules in the Immune System
In contrast to the molecules that were originally discovered in the immune system and later found to have functions in the nervous system, several molecules, such as Protocadherin (Pcdh), and the Eph/Ephrin and Semaphorin families, were first reported in the nervous system. However, they are also regarded as immune-modulatory molecules. Pcdh18 is an activation marker of CD8+ memory T cells that can function as an inhibitory signaling receptor and restrict the effector phase (Vazquez-Cintron et al., 2012). Ephrin-B1(Efnb1) is a specific marker for germinal center (GC) and memory precursor B cells (Laidlaw et al., 2017), and Efnb1 repulsively inhibits GC recruitment and retention of follicular T helper (Tfh) cells. This repulsion requires forward signaling through Eph-B6 on Tfh. Efnb1 also promotes GC Tfh production of IL-21 through forward signaling via Eph-B4 (Lu et al., 2017). Semaphorins, major axon guidance molecules, are also involved in the various phases of physiological and pathological immune responses associated with rheumatoid arthritis, systemic lupus erythematosus, systemic sclerosis and anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis. For example, Sema3A synthesized by activated dendritic cells and T cells downregulates T cell proliferation, activates macrophages, and is also involved in DC transmigration across the lymphatics. Sema4A is related to T cell priming and Th1/Th2 regulation and maintenance of Treg stability (Kumanogoh and Kikutani, 2013; Nishide and Kumanogoh, 2018).
Perspective on Future Directions
As discussed above, the CNS and immune system share many common characteristics; however, some clear fundamental differences do exist, especially with regard to the manner of target molecule/cell recognition. Immune cells can dynamically move around to search for targets and can clonally expand in cell number. The primary means of communication between immune cells include direct contacts with nearby cells that are attracted by chemokines or via secretory molecules. In the nervous system, mature neurons themselves do not proliferate or actively migrate; therefore, where a neuron is located during development is critically important. Moreover, the specific order of signaling between cells in a neural network is essential. For example, when an excitatory neuron A directly projects to neuron B, neuron A would activate neuron B. In contrast, if neuron A indirectly communicates with neuron B through an inhibitory neuron C (i.e., A→C→B), neuron B would be suppressed by the activation of neuron A. The formation of these specific neuronal connections could, if not exclusively, be accomplished by specific and diverse cell adhesion molecules, such as Dscam (Schmucker and Chen, 2009) and clustered Pcdh (Yagi, 2008). For example, the Drosophila Dscam gene could theoretically generate 38,016 isoforms (19,008 for the extracellular domain) by alternative splicing. Interestingly, the Dscam protein is also detected in Drosophila immune-competent cells (hemolymph) and is believed to be involved in bacterial binding followed by phagocytosis, suggesting that this molecular diversity may provide a highly diverse innate immune system in insects (Watson et al., 2005). In these examples, extraordinary diversity and specificity, shared by the nervous system and immune system, may be established based on a common molecular machinery or operational modes between these two systems. From this perspective, to understand the mechanisms of development of the complex brain network, significantly more effort should be directed at uncovering why some molecules or cells that are known to work in acquired immunity are expressed/exist in the developing nervous system.
KM and KN wrote the manuscript.
This work was supported by the Ministry of Education, Culture, Sports, Science and Technology (MEXT)/Japan Society for the Promotion of Science (JSPS) Grants-in-Aid for Scientific Research (KAKENHI) (JP17J04561, JP18K14841, JP16H06482, and JP18K19378), the Naito Foundation, the Takeda Science Foundation, the Keio Gijuku Academic Development Funds, and Keio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and Research.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: MHC, complement, T cell, central nervous system, immune system
Citation: Morimoto K and Nakajima K (2019) Role of the Immune System in the Development of the Central Nervous System. Front. Neurosci. 13:916. doi: 10.3389/fnins.2019.00916
Received: 26 April 2019; Accepted: 16 August 2019;
Published: 03 September 2019.
Harold Cremer, Centre National de la Recherche Scientifique (CNRS), France
Copyright © 2019 Morimoto and Nakajima. 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: Kazunori Nakajima, firstname.lastname@example.org