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First published online June 6, 2008
doi: 10.1242/10.1242/dev.020511
Meeting Review |
Department of Neurobiology, University of Chicago, Chicago, Il 60637, USA.
e-mail: egrove{at}bsd.uchicago.edu
SUMMARY
The RIKEN Center for Developmental Biology recently held its 2008 Symposium `Turning Neurons into a Nervous System' in Kobe, Japan. The program, organized by Masatoshi Takeichi, Joshua Sanes, Hideki Enomoto and Raj Ladher, provided a rich sampling from current work in developmental neurobiology. Researchers from Japan, Europe and the USA gathered at this meeting to share insights into neural development and to admire the opening of the cherry blossom season.
Introduction
True to its name, the symposium began with a talk by William Klein (M.D. Anderson Cancer Center, TX, USA) on retinal ganglion cell specification and ended with Barry Dickson (Research Institute of Molecular Pathology, Vienna, Austria) describing the genetic control of mating behavior. From Drosophila to humans, the major model systems were well represented at this meeting, including the mouse-the mammalian model of choice. Participants in the meeting were fortunate to hear a special lecture from one of the founders of modern mouse genetics: Nobel Laureate, Mario Capecchi (HHMI, University of Utah, UT, USA).
As at any developmental neurobiology meeting, an overarching theme was the balance of hardwired and activity-dependent mechanisms at each stage of development. Both mechanisms were proposed to shape the distinctive dendritic and axonal arbors that characterize particular types of neuron. Several talks emphasized the hardwired nature of early development in sensory systems. There was equal emphasis, however, on the mechanisms of postnatal plasticity, which might, under the right circumstances, reshape even the adult brain. The disruption of activity-dependent mechanisms that mold the postnatal brain was, moreover, the center of a bold new hypothesis regarding the genetics of autism. Each of these sub-themes is discussed in more detail below.
From new cells to new models
A new cell type
For well over a hundred years, neuroanatomists have catalogued the
morphological features of different neuron types and speculated on their
functional correlates. Surprisingly, the diversity of neuron types is still
not fully appreciated. Joshua Sanes (Harvard University, MA, USA) described a
previously unknown class of retinal ganglion cells (RGCs), revealed by the
transgenic labeling of cells that express the junctional adhesion molecule B
(Kim et al., 2008
). These RGCs
are scattered across the mouse retina with their dendrites aligned from dorsal
to ventral (Fig. 1A). The cells
respond to stimuli that move across the retina from dorsal to ventral, a
striking example of the functional significance of arbor shape. Because the
lens of the eye inverts the image that falls on the retina, these RGCs detect
upward motion in the outside world. Why a specific cell population should be
set aside for this function remains a mystery, and suggests that other,
equally specialized, retinal cells will eventually be found.
Novel axon guidance cues
A half dozen established families of guidance molecules dominate the field
of axon guidance. Vascular-derived endothelins (Edns) are newcomers, and were
discussed by Takako Makita from David Ginty's laboratory (HHMI, Johns Hopkins
University School of Medicine, MD, USA)
(Makita et al., 2008). As
presented by Makita, this lab's findings show that newly born sympathetic
neurons in the mouse embryo follow vascular trajectories for guidance, adding
to a growing appreciation of the role that surrounding non-neural tissues have
in regulating neural development.
Autism and activity-dependent genes
Autism is characterized by impaired social interactions and language use,
indicative of a profound disruption to brain function that might be
particularly devastating to early childhood development. The pattern of
inheritance of autism indicates that it is due to mutations at several,
potentially interacting, loci. Christopher Walsh (HHMI, Harvard Medical
School, MA, USA) used single nucleotide polymorphism (SNP) genotyping to
search for autism-related mutations in families with high rates of autism. The
list of candidate genes overlapped with a set of genes defined as `activity
dependent' in an independent study by Michael Greenberg (Harvard University,
MA, USA). These collaborative findings suggest the provocative hypothesis
that, in autism, activity-dependent processes that are crucial to normal
postnatal development are impaired (Morrow
et al., 2008).
Neuronal polarity and dendrite patterning
Mineko Kengaku (Riken Brain Science Institute, Wako, Japan) proposed a role for activity- and innervation-dependant mechanisms in shaping the dendritic arbor of a cerebellar Purkinje cell. The mature arbor lies flat in a single sagittal plane, but an immature Purkinje cell extends dendrites in multiplanar arrays (Fig. 1B). The elimination of excess dendrites accompanies the elimination of multiple climbing fibers that contact the immature Purkinje cell. Only one climbing fiber will innervate the mature neuron. If climbing fibers are inefficiently removed in mouse mutants, or if they are synchronously activated, the multiplanar tree is not remodeled.
Dendritic trees form under two broad constraints, with details specific to neuronal cell type. Branches of the same neuron divide and separate in a cell type-specific manner, and the entire arbor may either avoid the arbor of a neighboring neuron or overlap with it. This suggests a system of identity recognition by which neurons distinguish self from non-self. The most detailed model of identity recognition by neurons has been worked out in Drosophila, following the identification of orthologs of the mammalian gene Dscam (Down's syndrome cell-adhesion molecule). Alternative splicing of Dscam in Drosophila, but not in vertebrates, generates several thousand different receptor isoforms that display homophilic binding.
Dietmar Schmucker (Harvard Medical School, MA, USA) discussed
`self-avoidance' between dendrites of the same neuron, mediated by receptor
isoforms of Dscam (Hughes et al.,
2007). Dendrite arborization (da) neurons in Drosophila
larvae extend two-dimensional dendritic trees. Loss of Dscam causes the
dendrites of an individual da neuron to clump together; introducing a single
Dscam isoform into a neuron restores dendrite separation. In a subset of da
neurons, the dendritic arbors of neighboring cells avoid one another. This
dendritic `tiling' is unaffected by the loss of Dscam. However, segregated
arbors can be forced to tolerate one another, and to overlap, by introducing
different Dscam isoforms in each cell. Equally, two overlapping arbors can be
forced to separate by introducing a single isoform of Dscam in both cells.
|
). Zipursky also presented data from studies of Dscam at the
atomic level, identifying the structural elements that allow isoform-specific
homophilic binding (Meijers et al.,
2007; Wojtowicz et al.,
2007).
Adrian Moore (Riken Brain Science Institute) used the model system of
Drosophila da neurons to identify transcription factors that control
arbor complexity. Class IV da neurons have the most complex dendrite arbors
and express both Cut and Knot. Both Cut and Knot
transcription factors promote dendrite complexity. Knot induces
microtubule-filled extensions to form in da neurons, mediated by Spastin, a
protein that is involved in severing microtubules. Cut additionally induces
dendritic filipodia, an activity that is suppressed by Knot in class IV cells,
which do not generate dendritic filipodia as a result
(Jinushi-Nakao et al.,
2007).
Historically, the topic of neuronal polarity has focused on how one of
several cell neurites is specified to become the axon. Kozo Kaibuchi (Nagoya
University Graduate School of Medicine, Nagoya, Japan) discussed the
development of the directional trafficking of proteins along the growing axon.
Collapsin response mediator protein 2 (CRMP2) links vesicles that contain the
neurotrophin receptor TrkB to the microtubule motor kinesin 1, allowing the
kinesin 1-mediated axonal transport of TrkB. Activation of TrkB in turn
promotes axon growth. Glycogen synthase kinase 3β (GSK3β) blocks the
formation of this complex by phosphorylating CRMP2, giving GSK3β a role
in regulating neural polarity, and implying that it must be inactivated in a
growing axon. Indeed, GSK3β appears to be selectively inactivated at the
distal end of growing axons (Jinushi-Nakao
et al., 2007).
Cerebral cortex development
Development of the cerebral cortex requires several cell types to acquire
polarity, among them the radial glial (RG) cell, which generates neurons and
extends a process from the ventricle to the pial surface along which newborn
neurons migrate. William Snider (University of North Carolina, NC, USA)
provided evidence that GSK3
/GSK3β and Adenomatous polyposis coli
(APC), a substrate of GSK3β, are regulators of RG cell proliferation and
polarity. The double deletion of Gsk3b and Gsk3ain the
cortex of mouse embryos caused hyperproliferation and disrupted RG cell
morphology. The conditional deletion of Apc caused an even more
dramatic disturbance. Videomicroscopy showed RG processes that appeared to be
lost: their leading edges moving randomly, rather than heading for the pial
surface.
A major step in corticogenesis is the development of a two-way pathway
between cortex and thalamus that crosses the striatum and the globus pallidus.
Previous studies have shown that thalamocortical axons receive important
permissive and instructive guidance cues along this route
(Garel and Rubenstein, 2004;
Lopez-Bendito et al., 2006).
Masatoshi Takeichi (RIKEN Center for Developmental Biology, Kobe, Japan)
reported that the pathway between thalamus and cortex fails to develop in mice
deficient in OL-protocadherin (also known as protocadherin 10, Pcdh10).
OL-protocadherin is expressed in the striatum, and several findings point to
the striatum as being the site at which axons are blocked in the mutant. The
striatonigral pathway is absent and striatopallidal axons are tangled. In
vitro, however, axons grow out from dissociated striatal neurons, suggesting
that growing striatal axons - and by extension, other axons crossing the
striatum - face an inhospitable environment
(Uemura et al., 2007).
Takeichi provided evidence that OL-protocadherin acts on axonal outgrowth by
associating with the Nap1-WAVE protein complex, which is known to regulate
cell motility.
Aaron DiAntonio (Washington University School of Medicine, WA, USA)
reported a similar loss of connections between thalamus and cortex following
deletion of the mouse ortholog of highwire, Phr1
(Bloom et al., 2007)
(Mycbp2-Mouse Genome Informatics). A comparison between mice in which
Phr1 was conditionally knocked out in the entire telencephalon, or
just in the cortex, suggested that the key deficit is in the subcortical
telencephalon. Although an Islet1-expressing permissive corridor for
thalamic axons (Lopez-Bendito et al.,
2006) is present in the constitutive Phr1 mutant,
striatopallidal axons again form a tangle. Together, these findings suggest
that several permissive conditions are important for the development of the
pathway between thalamus and cortex, including the normal growth of axons from
local neurons along the pathway.
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William Klein (University of Texas, TX, USA) described a transcription
factor network that is required for competence to acquire an RGC fate, for RCG
fate specification and for the differentiation of RCGs
(Mao et al., 2008;
Mu et al., 2005). A mouse
homolog of the Drosophila proneural gene, atonal, Math5
(Atoh7-Mouse Genome Informatics) is required for competence and
specification. [Note that the zebrafish lakritz mutant discussed
below (Fig. 2) lacks Atoh7 and
has no RGCs.] Subsequently, the interplay between Math5 and Brn3/Pou4f2,
together with Isl1, suppresses Math5 so that RCG differentiation can proceed.
Pou4f2 further regulates the expression of eomesodermin, a transcription
factor that mediates the later differentiation of RCG cells, including
myelination. In presenting his gene regulatory network for RGC cells, Klein
proposed the intriguing hypothesis that relatively simple transcriptional
networks generate specific neuron types, involving dozens (but not hundreds)
of transcription factors.
The output from RGCs to the brain is modulated by interneurons that make
synaptic contact with RGC dendritic arbors in the inner plexiform layer (IPL)
of the retina. Joshua Sanes presented evidence that four highly related
molecules, Dscam1 and 2, and sidekicks (Sdk) 1 and 2, are required to match up
the correct synaptic partners in the correct sublaminae of the IPL
(Yamagata and Sanes, 2008).
The four molecules mediate homophilic adhesion (not repulsion this time) and
are distributed in appropriate, coordinated patterns in the retina. Thus,
Dscams and similar receptors can provide at least a simple recognition code in
the vertebrate nervous system.
The projection from the retina to the optic tectum (or superior colliculus)
is a classic model system for studying topographical map formation in the
brain. Neighboring RGCs project to neighboring tectal neurons to generate a
continuous map of the visual field in the tectum. Axons from cells along the
temporal to nasal axis of the retina, for example, project to neurons along
the anterior to posterior axis of the tectum
(Fig. 2A). Temporal RCG axons
are directed to the anterior tectum by repellant ephrin A/EphA signals in the
posterior tectum, but it is unclear how nasal RGC axons are guided to the
posterior tectum. One possibility is that unknown molecular guidance
mechanisms direct nasal axons; another is that competition among axons for
anterior tectal space results in nasal retinal axons being pushed to the
posterior. Herwig Baier (University of California at San Francisco, CA, USA)
described elegant experiments that appear to settle the question, at least in
zebrafish. Small clones of wild-type cells were introduced into zebrafish
lakritz mutants, which lack RGCs. Some resulting chimaeras had eyes
with a single wild-type RGC. Regardless of the position of the RGC in the
retina, it projected to the correct target position in the tectum. In
particular, axons from nasal RGCs grew straight to the posterior tectum
(Fig. 2B). These findings
indicate that axon-axon competition is not required for retinotectal mapping
(Gosse et al., 2008), although
competition may be needed to regulate arbor size. Interestingly, this study
generally supports a previous computational model of retinotectal development
(Yates et al., 2004).
Plasticity and experience-dependent rewiring
Shortly after birth, many species pass through `critical periods' of neural plasticity during which their brains are particularly malleable to experience. Sensory systems are refined, and a variety of species-specific behaviors are learned. Ocular dominance plasticity is a favored experimental model for studying this phenomenon. Monocular visual deprivation (MD) in young mammals weakens the synaptic circuitry that underlies the visual cortical responses to the deprived eye, and strengthens the synaptic circuits that mediate responses to the non-deprived eye.
Only in recent years has plasticity in visual cortical responses to the two eyes been studied in mice, leading to a range of experimental approaches that are impracticable in cats or monkeys. Takao Hensch (Harvard University, MA, USA) presented new findings implicating the transcription factor Otx2 in visual cortex plasticity. Cortical infusion of Otx2 accelerates the overall response to MD in the primary visual cortex (V1). This effect is mediated through GABAergic interneurons that contain parvalbumin (PV). Otx2 regulates the maturation of these PV interneurons, which in turn trigger general V1 plasticity. A conditional deletion of Otx2 in the visual pathway prevents plasticity, and this is reversible by benzodiazepine, a GABA-receptor agonist. Of note is that Otx2 appears to regulate the activity of interneurons but is not expressed in them. A daring hypothesis, well supported by the data presented, is that Otx2 is made by cells elsewhere in the visual pathway, and is then transported to and released in the visual cortex.
Tobias Bonhoeffer (Max Planck Institute for Neurobiology, Martinsried,
Germany) presented evidence that the adult mouse remains sensitive to MD,
showing results from technically impressive optical imaging experiments in
which dendritic spines in the mouse V1 were imaged before, during and after
MD. After 1 week of deprivation, which is longer than is required to induce
plasticity in juvenile animals, cells in the binocular region of V1 increased
their response to the stimulation of the non-deprived eye. Additionally,
dendrites imaged in the binocular region increased their number of spines by
5-25%. After deprivation, visual responses and spine densities returned to
normal. However, plasticity can be elicited again with a new, shorter period
of monocular sight deprivation, indicative of the first deprivation having a
priming effect. This time too, plasticity lasts for longer, indicating that
repeated experience enhances cortical plasticity
(Hofer et al., 2006).
Conclusion
At this meeting, a remarkable number of excellent talks and posters of unpublished data were presented, many of which could not be discussed in this review. Among the themes not covered here is synaptogenesis, a central interest of many of the researchers present. Notably, this field still lacks candidate molecules that actually induce synapses to form in the CNS of vertebrates. Previous candidates, such as neurexins and neuroligins induce synapses in vitro, but in vivo have other important roles, for example in promoting synaptic function. Key talks on self- and other recognition by neurons in Drosophila raise the issue of whether genes exist in vertebrates that can generate multiple cell labels, as the Dscam genes do in Drosophila. Finally, the day of identifying individual disease susceptibility genes from different families may be over. Broad screens of the genome of large, interrelated families appears much more likely to solve the problem of the genetic causes of complex mental health disorders.
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