Our sophisticated thoughts and behaviors are based on the miraculous development of our complex nervous network system, in which many different types of proteins and signaling cascades are regulated in a temporally and spatially ordered manner. Here we review our recent attempts to grasp the principles of nervous system development in terms of general cellular phenomena and molecules, such as volume-regulated anion channels, intracellular Ca2+ and cyclic nucleotide signaling, the Npas4 transcription factor and the FLRT family of axon guidance molecules. We also present an example illustrating that the same FLRT family may regulate the development of vascular networks as well. The aim of this review is to open up new vistas for understanding the intricacy of nervous and vascular system development.
The nervous system has a complex but highly organized structure, providing the basis for our complex and sophisticated thoughts and behaviors. The development of the nervous network system is thus nothing short of a miracle, with many different kinds of proteins and signaling cascades being up- and downregulated in a temporally and spatially ordered manner during this process. One effective approach to gaining an understanding of the principles of nervous system development is to explore commonalities and variations in general cellular phenomena and molecules. In this review, we focus on the functions of ion channels, intracellular calcium ion (Ca2+) and cyclic nucleotide signaling, transcription factors and axon guidance molecules to understand the rules of nervous system development. Interestingly, we also describe how some of these rules are applicable to the development of vascular networks as well. Our aim is to open up new vistas for understanding the intricacy of nervous and vascular system development.
Roles of volume-regulated anion channels during neuronal migration in the developing brain
During proliferation, migration, neurite extension and retraction, among other processes, the cell volume of developing neurons changes dynamically. Cell volume regulation is an essential function in all types of cell and is achieved through regulation of the net influx or efflux of solutes, which is accompanied by passive water movement, across the plasma membrane. The volume-sensitive outwardly rectifying (VSOR) anion channel is a major regulator of anion flux during cell volume regulation and is present on all types of vertebrate cells as the most dominant form of volume-regulated anion channels [1–5]. The VSOR channel is activated in response to cell swelling induced by hypotonic or excitotoxic stimuli or, alternatively, to receptor activation without cell swelling. Opening of the channel provides anions, mainly chloride ions (Cl−), with a pathway through the cell membrane, which in turn may induce either the net influx or net efflux of solutes across the membrane with the help of the electrochemical driving forces of other cations, such as sodium (Na+) ions for influx or potassium ions (K+) for efflux; this process results in an increase or a decrease in cell volume, respectively. The VSOR channel is also permeable to excitatory amino acids, such as glutamate and aspartate, and as such may also play a role in signaling between adjacent cells, especially in the central nervous system (CNS) [5, 6]. Activation of the VSOR channel through triggering by receptor activation is regulated in the immediate vicinity of the activated receptor molecules. In earlier studies carried out by our group (T. Akita) in astrocytes, this activation was found to be mediated by Ca2+-dependent kinases that are activated in regions containing a very high concentration of intracellular Ca2+ within nanometers of the Ca2+-permeable ion channels—the so-called Ca2+ nanodomains [7, 8]. This mechanism provides a basis for selective activation of a limited number of VSOR channels located on a part of the cell surface where a small number of receptors are locally activated, and it is this local activation which may drive the changes in local cell volume required for morphological changes of the cell .
Biophysical and pharmacological characteristics of the VSOR anion channel differ somewhat between cell and tissue types [3, 5]. These characteristics and the roles of the channel have been well explored in the mature CNS, whereas they are still poorly understood in the immature nervous system . Critical roles of the VSOR anion channel in cell proliferation, migration, differentiation and programmed cell death have been elucidated during development in other biological systems [9–11], strongly indicating that it also plays critical roles during nervous system development, as recently found during cerebral cortex development. There are two major streams of neuronal migration in the developing cortex: tangential migration of gamma-aminobutyric acid (GABA)ergic interneurons originating from the ganglionic eminences in the ventral forebrain and radial migration of glutamatergic pyramidal and spiny stellate neurons from the adjacent ventricular zone lining the dorsal telencephalic ventricles in the fetal brain (Fig. 1a). It has long been suggested that GABA released from migrating interneurons regulates the speed of radial migration of glutamatergic neurons [12–15]. We recently confirmed that blockade of GABAA receptors with SR95531 accelerates radial migration , leading to the conclusion that activation of GABAA receptors slows the migration, presumably for proper development of the cerebral cortex. Interestingly, we further found that the major endogenous agonist of GABAA receptors during the radial migration is taurine released through the VSOR channels from neurons—and not GABA . Taurine is known to act as an agonist of the receptors for glycine and GABA [17–19]. In the mature brain, the cytoplasm of both neurons and glia contain taurine at concentrations of 10–20 mM , whereas in the embryonic brain the taurine content is five- to tenfold higher [21, 22]. We also observed that taurine is enriched in the marginal zone (MZ) and in the subplate (SP) of the fetal neocortex  (Fig. 1b), suggesting that both the Cajal-Retzius neuron in the MZ and the SP neuron secrete taurine. Permeability of the VSOR channel to taurine has been demonstrated in mature neurons and glia [23–26] and, more recently, also in neural stem/progenitor cells obtained from both embryonic and adult brains . However, the mechanism of just how VSOR channels are activated to release taurine during the radial migration is not yet resolved. Activation of GABAA receptor Cl− channels depolarizes the membrane of migrating embryonic neurons due to their reversal voltage for Cl− being higher than their resting membrane voltage , and this induces the opening of voltage-gated Ca2+ channels and intracellular oscillatory Ca2+ signaling [12, 15, 27]. If the VSOR channels located at the leading edges of migrating neurons are activated through Ca2+ nanodomains of the oscillatory signaling process, the resulting Cl− efflux with the help of K+ efflux would promote shrinkage of the edges. Therefore, taurine-mediated GABAA receptor activation might enhance VSOR channel activation at the edges of migrating neurons when the edges reach the taurine-rich regions, and this might put a brake on the migration (“VSOR channel hypothesis”; Fig. 1b).
As a regulator of cell volume and intercellular signaling, the VSOR anion channel is likely to play important roles not only in radial migration, but also in tangential migration, proliferation and differentiation of the networks of neurons and glia in the developing brain. It has been demonstrated that normal brain assembly in embryos, including cortical layer formation, axonal fiber projection and morphological synapse formation, depends on neurotransmitters that must be released through as yet unidentified mechanisms that differ from vesicular exocytosis [28, 29]. Therefore, exploring in detail the modes of activation of the VSOR channel and how these relate to the developing processes would shed light on the mystery of fetal brain development in the near future.
Control of neuronal migration by extrinsic and intrinsic programs through modulating Ca2+ and cyclic nucleotide signaling
Newborn neurons often exhibit spontaneous elevations of intracellular Ca2+ level. In this section, T. Kumada discusses results showing that both extrinsically and intrinsically determined patterns of intracellular Ca2+ fluctuations and their interactions with cyclic nucleotide signaling control the speed, mode and direction of neuronal migration. Komuro and Rakic originally demonstrated the relationship between Ca2+ fluctuations and neuronal migration using time-lapse Ca2+ imaging of granule cells migrating from a microexplant of the postnatal cerebellum in culture . These authors noted that the amplitude and frequency of Ca2+ transients in isolated granule cells are positively correlated with the rate of cell movement. In the cerebellar tissue, granule cells change their mode of migration during their trajectory; after they tangentially migrate at the fastest rate in the external granular layer, they change the direction from tangential to radial toward the internal granular layer, where they terminate their migration  (Fig. 2a). Using cerebellar slice culture preparations, Kumada and Komuro confirmed that granule cells exhibited distinct patterns of Ca2+ transients and rates of cell movement in different cerebellar cortical layers, that the frequency of Ca2+ transients was indeed positively correlated with the migration speed during the whole trajectory and finally that the Ca2+ transients ceased before termination of their migration [32, 33] (Fig. 2a). Increasing and decreasing the frequency of Ca2+ transients by experimentally altering the Ca2+ influx increased and decreased the migration speed, respectively, and experimentally eliminating the Ca2+ transients induced a premature termination of migration . Thus, the results confirmed that the layer-specific pattern of Ca2+ transients controls the speed of granule cell migration in each cortical layer. Similar regulation has also been reported in tangentially migrating GABAergic interneurons in the developing neocortex . However, in contrast to these observations, an increase in Ca2+ oscillation frequency has been shown to induce termination of the radial migration of glutamatergic neurons in the developing neocortex [15, 35, 36]. Ca2+ signaling dynamically interacts with the signaling cascades mediated by other second messengers, such as cyclic adenosine monophosphate (cAMP) . By pharmacologically manipulating cAMP and cyclic guanosine monophosphate (cGMP) levels, our group revealed that cAMP signaling acts as a brake on granule cell movement, while cGMP signaling acts as an accelerator . Activation of cAMP signaling decreases the frequency of Ca2+ transients, and this is one of the causes of the decrease in granule cell motility, while activation of cGMP signaling does not affect this frequency .
Depolarizing neuronal activity mediated by neurotransmitters increases the frequency of Ca2+ transients through activation of voltage-gated Ca2+ channels (VGCC), and this may regulate neuronal development prior to synaptogenesis [40, 41]. Komuro and Rakic were the first to show that the N-type VGCC and the NMDA (N-methyl-d-aspartate) subtype of glutamate receptor facilitate granule cell migration in the cerebellar tissue [42, 43]. In immature neurons, GABA also acts as an excitatory neurotransmitter and increases the Ca2+ transient frequency through VGCC activation [15, 27, 35]. The excitatory GABA action is based on raised intracellular Cl− concentrations due to Cl− uptake through the Na+–K+–Cl− cotransporter 1 (NKCC1) in immature neurons . Developmental or experimental expression of Cl−-extruding K+–Cl− cotransporter 2 (KCC2) converts the excitatory action of GABA into an inhibitory action, which reduces the Ca2+ fluctuation frequency and may vary the mode of neuronal migration [34, 45, 46]. This developmental switch in the action of GABA is controlled by cell-intrinsic programs during neuronal differentiation . In addition to VGCC, the release of Ca2+ from internal Ca2+ stores is also involved in the regulation of neuronal migration . Although Ca2+ signaling is known to play a pivotal role in organizing the cytoskeleton, precise detailed knowledge of just how Ca2+ signaling determines the dynamic behavior of developing neurons and the mode of neuronal migration is still lacking.
External cues provided by axon guidance molecules are also known to play important roles in neuronal migration. Some guidance molecules, such as Slit, may induce Ca2+ elevation in the leading processes of migrating neurons in a manner similar to that observed in axonal growth cones [48–50]. Slit-2, a chemorepellent to cerebellar granule cell migration, induces a propagating Ca2+ wave from the leading process to the soma, which is mediated by Ca2+-induced Ca2+ release from the internal stores . Sonic hedgehog, another guidance molecule, also acts as an important trigger of Ca2+ signaling-mediated neural activity, inducing neuronal differentiation . These processes suggest the importance of links between individual external cues and distinct modes of Ca2+ signaling. At specific turning points, the migrating neurons may change their responsiveness to an external cue, as seen in axonal guidance . Interestingly, the intracellular balance between Ca2+ levels and different cyclic nucleotide signaling activities may determine the responsiveness of the migrating neuron to a guidance cue. For example, in embryonic spinal neurons of Xenopus laevis, a higher ratio of cAMP/cGMP in response to netrin-1 binding to DCC (deleted in colorectal cancer) increases Ca2+ currents through VGCCs and intracellular Ca2+ release, resulting in growth cones being attracted to the guidance cue, whereas a lower ratio in response to netrin-1 binding to the DCC–Unc5 complex decreases the Ca2+ currents and Ca2+ release, resulting in repulsion from the cue .
In addition to external cues, which are essential for the selection of migratory paths, cell-intrinsic programs also control neuronal migration. The speed and mode of migration of isolated granule cells dynamically change even without cell–cell contact and in the absence of external guidance cues [54, 55]. The migrating isolated cells exhibit autonomous changes in the direction of migration (i.e. turning) and in the shape of their leading and trailing edges. The changes can be subdivided into several distinct modes of turning, and the cellular morphology in each mode is similar to that observed in the cerebellar tissue  (Fig. 2b). Thus, the changes must be regulated by cell-intrinsic (internal clock) programs, and we have found that Ca2+ and cyclic nucleotide signaling cascades are also involved in these programs [39, 55]. For example, in isolated granule cells, the frequency of Ca2+ transients, which positively correlates with their migration rate, depends on the elapsed time after plating, and termination of their migration is always preceded by a loss of Ca2+ transients, as occurs after 50–60 h of migration in the cerebellar tissue  (Fig. 2a). Importantly, experimental manipulations of Ca2+ and cyclic nucleotide signaling pathways in isolated cells vary the speed of migration, the frequency of turning and the preference for a turning mode in the same way as in the tissue  (Fig. 2b). Thus, the Ca2+ and cyclic nucleotide signaling cascades driven by intrinsic programs regulate the autonomous turnings of migrating granule cells in isolated conditions. The mechanism by which the intrinsic programs drive the signaling cascades, however, remains to be elucidated. The autonomous changes in Ca2+ and cyclic nucleotide signaling by intrinsic programs suggest that the programs may also affect the role of external guidance molecules in directing neuronal migration through regulating the basal activity of these signaling pathways. The mechanism of just how intrinsic programs interact with external cues through Ca2+ and cyclic nucleotide signaling is an important issue which needs to be addressed.
Taken together, Ca2+ and cyclic nucleotide signaling not only mediate the responses to external guidance cues, but they also modulate the responsiveness to guidance cues and control neuronal migration even in the absence of external cues based on cell-intrinsic programs. The intrinsic programs may change the role of external guidance molecules by altering Ca2+ and cyclic nucleotide signaling pathways. Thus, both the speed and the fate of neuronal development must be determined by orchestrated interactions between intrinsic programs and external cues through Ca2+ and cyclic nucleotide signaling.
Transcription factor neuronal Per/Arnt/Sim domain protein 4 (Npas4) regulates sensory experience-dependent development of dendritic spines in newborn olfactory bulb interneurons
Sensory experience regulates neural development in a variety of species and in various brain structures, including the cortex, hippocampus and olfactory bulb (OB) [56–59]. OB interneurons are a good model for studying the modification of neural circuits by sensory inputs from the external world during the postnatal stages. OB interneurons are generated throughout life in the subventricular zone, migrate along the rostral migratory stream and differentiate into GABA-releasing inhibitory interneurons, such as granule cells (GCs) and periglomerular cells (PGCs), in the OB [60–64] (Fig. 3a). Olfactory sensory deprivation or, alternatively, an odor-rich environment can promote suppression or acceleration, respectively, of dendritic morphogenesis and spine formation in newborn OB interneurons [65–71]. However, little is known about the molecular players or the precise mechanisms that integrate odor-induced activity with the developmental processes of OB interneurons.
Using DNA microarray technology and in situ hybridization screenings, our group (S. Yoshihara) newly identified a transcription factor coding gene, neuronal Per/Arnt/Sim domain protein 4 (Npas4), which is expressed in a subset of OB GCs following sensory experience . Npas4 is an immediate early gene activated by neuronal activity via Ca2+-dependent signaling pathways . The transcription factor Npas4 promotes the formation of inhibitory synapses in the developing visual system  and controls the homeostatic inhibitory/excitatory balance that regulates visual cortical plasticity . Moreover, Npas4 interacts with several promoters that are regulated by neuronal activity and mediates BDNF (brain-derived neurotrophic factor) expression in cortical pyramidal and hippocampal CA3 neurons [72, 74–76]. We performed gain- and loss-of-function experiments for the Npas4 gene in OB GCs, based on lentiviral gene transfer. Npas4 overexpression in newborn OB GCs increased the spine density even under sensory deprivation . Furthermore, Npas4 overexpression increased the number of puncta stained by either post-synaptic [post-synaptic density protein 95 (PSD-95) or gephyrin] or pre-synaptic (synaptoporin) markers in the distal region of GC dendrites . Conversely, both Npas4 knockdown and knockout significantly reduced the spine density of OB GCs . These results strongly suggest that Npas4 is both necessary and sufficient on its own for increasing sensory input-dependent synaptogenesis in OB GCs.
To identify the target genes through which Npas4 regulates synaptogenesis in OB interneurons, we performed ChIP-Seq analysis in homogenized OB tissues using the antibody against Npas4 and searched for the gene promoter regions that Npas4 can bind to. As a result, we identified, as a novel target of Npas4, an oncogenic E3 ubiquitin ligase Mdm2 gene that is expressed at low levels in the wild-type OB but at higher levels in the Npas4-knockout OB . Thus, we expected that Npas4 would suppress Mdm2 gene expression. The results of gain-of-function and knockdown experiments for Mdm2 using the lentiviral vector system showed that overexpression and knockdown of Mdm2 reduced and enhanced, respectively, the spine density of GC dendrites compared with controls , thereby confirming Mdm2 as a bona fide target gene of Npas4 whose expression is indeed suppressed by Npas4. To identify the protein targets through which Mdm2 regulates synaptogenesis in the OB interneurons, we next searched for those proteins expressed differentially between wild-type and two Npas4-knockout OB by iTRAQ quantitative proteomics analysis. Proteomics and cell-line analysis revealed that Mdm2 ubiquitinates and promotes degradation of a microtubule-associated protein, doublecortin (Dcx) . Immunohistochemistry studies revealed that the expression of Dcx protein in GC dendrites within both the external proximal layer and the GC layer was twofold lower in the Npas4-knockout OB than in the wild-type OB . Furthermore, overexpression and knockdown of Dcx using the lentiviral vector system enhanced and reduced, respectively, the spine density of GC dendrites compared with controls . These results reveal that Dcx plays an important role in increasing the dendritic spine density of the OB GCs. Taken together, our findings suggest that Npas4 inhibits Mdm2 expression, which in turn prevents ubiquitination and degradation of Dcx, thereby promoting the development of dendritic spines of OB GCs after sensory experience (Fig. 3b).
To reveal the physiological function of spine formation in OB GCs, we examined the odor discrimination learning and memory in OB-specific Npas4-knockout mice generated by the Cre and loxP system. Loss of Npas4 in OB GCs was found to impair the learning of discrimination between two related odors without affecting the olfactory detection ability . This result suggests that spine formation in interneuronal dendrites in the OB neural circuitry is required for odor-associated learning and memory. Hence, through the regulation of activity-dependent synapse development in OB GCs, Npas4 can play an important role in the formation of functional olfactory learning neuronal circuits.
FLRT3 is a Robo1-interacting protein that determines Netrin-1 attraction in developing axons
Axon guidance is the process by which axons navigate to encounter their appropriate synaptic partner within the developing nervous system. Together with neuron migration, axon guidance is one of the most important hallmarks of nervous system development, and much study on this process has rendered many important clues of how it is wired and functions. Results obtained from different animal models have revealed many of the basic principles and the molecular mechanisms involved in the process of axon guidance [77–79]. For example, the tip of the axon has a protrusion, called the “growth-cone,” which is a very motile structure actively exploring the environment for cues that “guide” the axons to reach the proper target. Many of these axon guidance cues have been characterized, and they include five large families, namely, the Netrin, Slit, Ephrin, Semaphorin and classical morphogen families. These cues are sensed by the growth cone through specific receptors located at the surface of the cone, and the receptors activate intracellular signaling cascades which ultimately modify cytoskeleton dynamics. This leads to an attractive or a repulsive response, depending on the cellular context and the type of axon guidance cue and receptor involved. Axon guidance is not continuous but rather a step-wise process in which axons encounter intermediate targets (e.g. the nervous system midline), where they have to make guidance decisions. One intermediate target affects the response to the next one by changing, for example, the composition of receptors at the surface of the growth cone [77, 80]. Moreover, the guidance of a particular set of axons is tightly controlled in time and space and very often is exquisitely coordinated with the migration of other axons or neurons . Interestingly, the molecular mechanisms of axon guidance are not restricted to the nervous system, and they have also been found to be involved in the development of other systems, such as the vascular system (see following section).
Strikingly, the number of cues and receptors involved in axon guidance is relatively low compared to the enormous complexity of the nervous system. Mechanisms of proteolytic cleavage of these proteins, posttranslational modifications, alternative splicing or the presence of co-receptors have been described to fine tune and expand the responses of a particular axon to the environment [80, 82, 83]. More recently, it has been reported in many different contexts that the combination of several axon guidance cues triggers a response that cannot be predicted by the response to any of the cues individually, indicating that axon guidance cues are able to crosstalk. The mechanisms underlying such crosstalk are not known, but this is currently a field of very active research in molecular neurobiology since this is a scenario that resembles more accurately the in vivo situation where axons are challenged with a combination of cues . Also, these studies most probably will provide new insights which will further our understanding of the process of axon guidance and nervous system wiring and function. In this section, recent research carried out by our group (J. Egea; see  for further information) will be discussed. This work has elucidated the crosstalk mechanism of two of the most well-characterized axon guidance cues, netrin and slit, in the development of the thalamocortical axons (TCAs). TCAs convey sensory (with the exception of olfaction) and motor information to the neocortex. They are arranged topographically, with rostral thalamic neurons projecting their axons into the motor cortex and intermediate and caudal thalamic neurons projecting their axons into the somatosensory and visual cortex, respectively. This arrangement is controlled by gradients of axon guidance cues in a ventral structure called the corridor which sorts the axons according to their final destination  (Fig. 4). Rostral TCAs (rTCAs) cross an area in the corridor with the higher expression levels of Netrin, which can be either repulsive if Netrin interacts with Unc5 receptors or attractive if it interacts with DCC receptors, and of Slit, which interacts with Robo receptors, typically triggering repulsion. In order to understand how rTCAs integrate these two signals, we challenged in vitro explant cultures of rostral thalamus with Netrin and Slit, either individually or in combination (Netrin + Slit). Surprisingly, Netrin did not induce any effect, whereas Slit induced repulsion on these axons. Interestingly, Netrin + Slit triggered a net attractive response on rTCAs but not on intermediate axons (iTCAs), a result that may explain the segregation of the two types of projection in vivo . In order to understand the mechanisms involved in the specific attraction of rTCAs towards Netrin + Slit, we performed several in vivo and in vitro experiments. We demonstrated that the axon guidance receptor Robo1, but not Robo2, was necessary for the attractive effect, suggesting that Slit was activating its canonical receptor in this context. We also observed that Netrin + Slit induced a strong increase of the DCC levels on the surface of the growth cone on rTCAs but not on Robo1 knockout rTCAs, suggesting that Robo1 signaling is required. This effect was specific since it was neither observed after the stimulation with Slit or Netrin individually, nor in iTCAs stimulated with Netrin + Slit. Taken together, these results strongly indicated that increased DCC levels are required for the attractive response triggered by Netrin + Slit in rTCAs. Surprisingly, basal levels of DCC, Robo1 and Unc5 were not different between rTCAs and iTCAs, suggesting that a different molecular identity, specific to rTCAs, was responsible for the different behavior towards Netrin + Slit stimulation between rTCAs and iTCAs. In our search for possible candidates we focused on the family of fibronectin leucine-rich transmembrane proteins (FLRT). This family comprises three members (FLRT1–3), all of which have been shown to be involved in a wide variety of functions, including cell adhesion during morphogenesis of the early mouse embryo [88–90], neuronal differentiation [91, 92], regulation of radial migration of pyramidal cells in the cortex by acting as repulsive cues for Unc5 receptors [93, 94], in the control of tangential dispersion of pyramidal cells in the cortex by homophyllic adhesion  and in synapse development . Among these, we observed that FLRT3 displayed a graded expression in the thalamus, from rostral-high to caudal-low. Moreover, we found Robo1 to be one of the candidates for binding to the intracellular domain of FLRT3 in a yeast-two hybrid screening, an interaction that we were able to confirm by co-immunoprecipitation and co-localization assays in transfected cells and in cultures of rTCAs. Based on these observations, we considered the possibility that FLRT3 could participate in the attraction of rTCAs towards Netrin + Slit. To test this possibility, we used FLRT3 knockout explants and observed that the increase in surface DCC levels upon Slit + Netrin stimulation did not occur in this experimental context and that FLRT3 knockout rTCAs were not attracted to Netrin + Slit, demonstrating that FLRT3 plays a key role in this attractive response. We reasoned that if FLRT3 was sufficient to trigger this effect, overexpression of FLRT3 in iTCAs, where FLRT3 expression is normally low, should lead these axons to respond to Netrin + Slit and acquire the projection behavior of rTCAs. Indeed, when FLRT3 was overexpressed in iTCAs, these axons switched their projection into more rostral areas of the cortex, where usually only rTCAs project. Consistent with this observation, rTCAs were found to be more fasciculated in FLRT3 knockout embryos, with a significant number of axons spreading towards medial parts of the cortex. How FLRT3 regulates the attraction towards Netrin + Slit is not clear, but we believe that the interaction with Robo1 changes the intracellular signaling in rTCAs in two ways: on the one hand, FLRT3 inhibits Robo1 repulsive signaling (indeed, the observed repulsion effect of rTCAs towards Slit alone is mediated by Robo2 and not by Robo1), while on the other hand, FLRT3 cooperates with Robo1 in the activation of DCC receptor trafficking to the growth cone surface, an effect that requires the activation of protein kinase A (PKA) signaling. We suggest there is a “threshold” of PKA activity that is achieved upon Slit stimulation through Robo1–FLRT3 and this threshold activity may induce an increase (although undetectable) of surface DCC levels. When Netrin is applied, Netrin binding to DCC raises the level of PKA activity sufficiently high to potentiate a positive feedback loop that induces a further increase of DCC, as previously reported .
In summary, these results demonstrate the key role of FLRT3 in the control of, specifically, rTCA projections (see Fig. 4). The presence of FLRT3 and the modulation of Robo1 signaling results in Slit being a permissive cue for Netrin to induce attraction. These axons respond to Netrin + Slit in a manner (attraction) that cannot be predicted by the effects of individual cues (Netrin, no effect; Slit, repulsion). This observation reinforces the notion that mechanisms of crosstalk between axon guidance cues are important to expand the repertoire of axonal responses during development of the nervous system. Crosstalk depends on the presence of specific molecular identities as, for example, FLRT3 in the rTCAs, which are regulated in time and space. It is important to point out that crosstalk is also context dependent since the same molecules can exert different effects in different tissues. For example, Netrin and Slit interact differently in callosal and commisural axons compared to rTCAs. In callosal axons in the forebrain, DCC, while crossing the midline to project into the contralateral cortex, exerts a hierarchical effect over Robo1 by inhibiting Robo1 signaling to allow crossing of the midline, a territory highly enriched with Slit . In contrast, in the commissural axons of the spinal cord that have crossed the floor-plate, a territory highly enriched with Netrin, into the contralateral side, Robo1 exerts a hierarchical effect over DCC by inhibiting Netrin attraction to avoid re-crossing of axons .
Roles of the FLRT and Unc5 protein families proteins in the development of the nervous and vascular systems
The vasculature forms an elaborated and massive network, much like the nervous system, through which oxygen and nutrients are supplied to all body tissues. During development and remodeling, arteries and veins are first formed by vascular endothelial cells and then supported by smooth muscle cells and pericytes [100, 101]. Tip cells, a subset of endothelial cells, undergo sprouting angiogenesis, leading to the formation of capillaries. Similar to the growth cone in neurons, these cells sense the extracellular environment (e.g. extracellular matrix, growth factors and guidance molecules) to determine their fate (e.g. growth/extension, retraction or diversion). It is well known that canonical axon guidance molecules, such as Netrin and Unc5, Slit and Robo, Semapholins and Neuropilin/Plexin, Ephrin and Eph, are also commonly identified during vascular system development [79, 102].
Unc5 family proteins (Unc5A-D) are known as the receptors for Netrin family proteins to induce axon repulsion during nervous system development (Fig. 5a). In the vascular system, the Unc5B receptor is expressed on endothelial cells, including arterial tip cells (Fig. 5b) . However, the endogenous ligand for Unc5B in the vascular system is still unknown (see below), and its identification has been a major focus of ongoing research in the field of vascular development since the discovery of the importance of Unc5B in vascular morphogenesis more than a decade ago . In this section of the review, potential ligands for Unc5B during vascular development based on the phenotypes of various knockout mice are discussed by S. Yamagishi.
Lu et al. reported that Unc5B is specifically expressed on the endothelial cells of arteries and that disruption of Unc5B genes in the mouse and zebrafish induces an aberrant morphology of tip-cell fillopodia, increased vessel branching and abnormal navigation of vascular network development . Larrivée et al. demonstrated that Unc5B is transiently expressed during the sprouting of capillaries from tumor implants, indicating involvement of Unc5B in angiogenesis . In retinal blood vessels, loss-of-function studies using the antibody or gene knockout against Unc5B demonstrated hypervascularization . Furthermore, most of the conventional Unc5B knockout mice die because of heart failure at embryonic day (E) 12.5 . Navankasattusas et al. subsequently reported that even selective knockout of Unc5B in vascular endothelial cells, using Tie2-Cre mice and Unc5B-floxed mice, is lethal at the same stage as the conventional one because of a placental problem: the number of robust vertical vessel stalks in the placental labyrinth layer is decreased in the conditional Unc5B knockout mice . Taken together, these results support a critical role for Unc5B in vasculature formation. By contrast, although in vitro experiments have shown that classical Unc5B ligands, namely Netrin-1, -4 and Robo-4, exert an Unc5B-dependent repulsive effect on tip cells, knockout mice of these ligands demonstrate only minor hypervascularization [103, 105, 107–109] and do not suffer from heart failure as do Unc5B knockout mice . These results imply the existence of other endogenous ligands for the Unc5B receptor for proper vascular development.
In the context of nervous system development, in 2011 we identified FLRT2 and FLRT3 as axon guidance molecules that produce a repulsive effect by binding to the Unc5B and 5D receptors (Fig. 5a; see preceding section) . Structural and biochemical bases for the FLRT–Unc5 binding were recently resolved by crystallography and the surface plasmon resonance assay . FLRT2 and FLRT3 are cleaved at their extracellular juxtamembrane region by matrix metalloproteinases, and the ectodomains are shed into the extracellular space (Fig. 5b). Binding of the FLRT2 ectodomain to the Unc5D receptor is a repulsive cue for axon guidance and neuronal migration. At E15.5 in mice, FLRT2 is strongly expressed in the cortical plate of the developing neocortex, while its receptor Unc5D is expressed in multipolar neurons, namely, future upper layer neurons, in the subventricular zone. Knockout of FLRT2 facilitates the radial migration of multipolar neurons whereas overexpression of Unc5D slows the migration . Thus, the repulsive cue produced by the FLRT2–Unc5D interaction would slow radial migration. Intriguingly, Unc5D expression in multipolar neurons is transiently downregulated when the neurons migrate through the FLRT2-rich cortical plate, presumably in order to avoid FLRT2 binding . In contrast, FLRT3 is expressed especially in the intermediate zone of the neocortex and the rostral part of the thalamus in E15 mice [85, 95]. Unc5B-positive thalamic neurons are strongly repelled by FLRT3 . The FLRT3–Robo1 coupling in rostral thalamocortical neurons plays an important role in the proper topographical projection of their axons into the neocortex (see preceding section).
In the embryonic cardiovascular system, FLRT2 is expressed in the epicardial sheet and the myocardium of the heart from E9.5 to birth, whereas FLRT3 is transiently expressed in these structures between E9.5 and E12.5 . FLRT3 is also expressed in the postnatal retina during development of Unc5B-expressing retinal blood vessels . Mice with a loss-of-function mutation in FLRT2 die at E11.5/12.5 due to blood pooling, superficial hemorrhage and pericardial edema . In FLRT2-deficient mice, the basement membrane between the epicardium and the myocardium is disorganized, and the epicardial layer is detached from the myocardium, indicating loss of epicardial integrity . Electron microscopy analysis showed that the surface of the epicardium in the FLRT2 mutant is ruffled and uneven and has small hollows . This phenotype shares similarity with that of the FLRT3 knockout embryo in more primitive embryonic structures, in which the basement membrane in the anterior visceral endoderm is highly disorganized and the hollows on the boundary between the visceral endoderm and the definitive endoderm are visible at the mid-streak stage at around E7 . When FLRT2 was ectopically overexpressed in the FLRT3-deficient embryoid bodies, the basement membrane disorganization was clearly improved . Thus, these results indicate that FLRT2 and FLRT3 have an identical function.
Although both Unc5B and FLRT2 mutant mice die at similar developmental stages, the phenotypes of these mutant mice differ somewhat. For example, the thin heart muscle wall in the FLRT2 mutant is not observed in Unc5B knockout mice, whereas the placental vascular defect in Unc5B knockout mice is absent in the FLRT2 mutant [90, 106]. We have also observed that overexpression of a dominant negative form of Unc5B, lacking its intracellular domain, in arterial endothelial cells in vitro does not block repulsive responses of the cells induced by FLRT2 (unpublished data). Conditional knockout mice of FLRT3, another candidate for the Unc5B ligand, produced using Sox2–Cre, which removes all of the FLRT3 genes in the entire embryo and in the labyrinth layer of the placenta, showed a hypervascular phenotype in the retina, similar to that seen in Unc5B knockout postnatal escaper mice [95, 107]. However, these FLRT3 conditional knockout mice are more likely to be born beyond the critical period when most Unc5B knockout mice die . Therefore, neither FLRT2 nor FLRT3 seems to be the unique endogenous ligand for Unc5B. Further analysis using knockout mice of both FLRT2 and FLRT3 or other unknown molecules is needed to identify the endogenous ligand for Unc5B.
In this review, we have mainly focused on nervous system development and attempted to elucidate its principles in terms of ion channels, intracellular signaling, transcription factors and axon guidance molecules. We have also discussed a similar regulation of vascular system development mediated by the same axon guidance molecules. For each molecular category mentioned in this review, there are a tremendous number of molecular subtypes. Nevertheless, some common schemes and principles can clearly be seen in the modes of crosstalk and interactions between different proteins and/or signaling cascades and also in the modes of cellular movement and morphological changes during the system development. We hope that the topics discussed in this review also provide some clues to the developing processes of other biological systems, such as the lymphatic, respiratory, digestive systems, among others, which are also complex and highly regulated in amazing ways.
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We are grateful to the members of Department of Neurophysiology in Hamamatsu University School of Medicine for useful discussions and suggestions on this work and to Gandhervin Kesavamoorhy for his critical reading and constructive comments on an early version of the manuscript. This work was supported by Grants-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (21790216, 23612008 and 26460293 to T.A.; 23111510 23500444 and 26350594 to T.K.; 20163368 and 25430010 to S.Yo.; 23700412, 25122707 and 26670090 to S.Ya.), from the Spanish MICINN (BFU2013-48563-P to J.E.) and from the FP7-PEOPLE-2011-CIG (PCIG9-GA-2011-293980 to J.E.). J.E. was a recipient of a short-term fellowship from the Japan Society for the Promotion of Science (S-14197).
Conflict of interest
The authors declare that they have no conflict of interest.
All authors contributed equally to this work in providing an comprehensive review of different aspects of the subject.
The topics discussed in this review were presented at the symposium entitled “New trends for research on the regulatory mechanism of neuronal development” during the joint meeting of the 120th Annual Meeting of the Japanese Association of Anatomists and the 92nd Annual Meeting of the Physiological Society of Japan, held at Kobe Convention Center on 23 March 2015.
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Akita, T., Kumada, T., Yoshihara, Si. et al. Ion channels, guidance molecules, intracellular signaling and transcription factors regulating nervous and vascular system development. J Physiol Sci 66, 175–188 (2016). https://doi.org/10.1007/s12576-015-0416-1
- Nervous system development
- Anion channel
- Intracellular signaling
- Transcription factor
- Axon guidance
- Vascular system development