The role of receptor/channel activity in neuronal cell migration.

Confocal laser microscopy, in conjunction with carbocyanine dyes and calcium-sensitive fluorescent indicators, was used in slices and explant cultures of developing cerebellum to study cellular mechanisms underlying a motility of neuronal cell migration. The results indicate that a combination of voltage- and ligand-activated ion channels cooperatively regulates Ca2+ influx into the migrating cells. We suggest that molecules, present in the local cellular milieu, affect cell motility by activating specific ion channels and second messengers that influence polymerization of stiff and contractile cytoskeletal proteins. This early interaction between postmitotic neurons and surrounding cells controls the rate of their movements, sculpts their shapes, establishes their positions, and, therefore, indirectly determines their identities to prior formation of synaptic connections.

[1]  P. Rakić,et al.  Dynamics of granule cell migration: a confocal microscopic study in acute cerebellar slice preparations , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[2]  D. Bentley,et al.  Cytoskeletal events in growth cone steering , 1994, Current Opinion in Neurobiology.

[3]  N. Spitzer Spontaneous Ca2+ spikes and waves in embryonic neurons: signaling systems for differentiation , 1994, Trends in Neurosciences.

[4]  N. Spitzer,et al.  Action potentials, calcium transients and the control of differentiation of excitable cells , 1994, Current Opinion in Neurobiology.

[5]  P. Rakic,et al.  Recognition, adhesion, transmembrane signaling and cell motility in guided neuronal migration , 1994, Current Opinion in Neurobiology.

[6]  P. Rakić,et al.  Unique profiles of the alpha 1-, alpha 2-, and beta-adrenergic receptors in the developing cortical plate and transient embryonic zones of the rhesus monkey , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[7]  Fang Liu,et al.  Glutamate-mediated astrocyte–neuron signalling , 1994, Nature.

[8]  Timothy A. Springer,et al.  The dynamic regulation of integrin adhesiveness , 1994, Current Biology.

[9]  D. Pow,et al.  Glutamate in some retinal neurons is derived solely from glia , 1994, Neuroscience.

[10]  P. Rakic,et al.  Identification of membrane proteins that comprise the plasmalemmal junction between migrating neurons and radial glial cells , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  Stuart G. Cull-Candy,et al.  NMDA-receptor channel diversity in the developing cerebellum , 1994, Nature.

[12]  J. McIntosh,et al.  Complex patterns of [125I]omega-conotoxin GVIA binding site expression during postnatal rat brain development. , 1994, Brain research. Developmental brain research.

[13]  Y. Jan,et al.  Changing subunit composition of heteromeric NMDA receptors during development of rat cortex , 1994, Nature.

[14]  Mu-ming Poo,et al.  Turning of nerve growth cones induced by neurotransmitters , 1994, Nature.

[15]  M E Greenberg,et al.  Calcium regulation of gene expression in neuronal cells. , 1994, Journal of neurobiology.

[16]  B. Sakmann,et al.  Developmental and regional expression in the rat brain and functional properties of four NMDA receptors , 1994, Neuron.

[17]  H. Cameron,et al.  Blockade of NMDA receptors increases cell death and birth in the developing rat dentate gyrus , 1994, The Journal of comparative neurology.

[18]  D. Rossi,et al.  The developmental onset of NMDA receptor-channel activity during neuronal migration , 1993, Neuropharmacology.

[19]  P. Rakic,et al.  Modulation of neuronal migration by NMDA receptors. , 1993, Science.

[20]  C. Shatz,et al.  Developmental mechanisms that generate precise patterns of neuronal connectivity , 1993, Cell.

[21]  W Wisden,et al.  The distribution of thirteen GABAA receptor subunit mRNAs in the rat brain. III. Embryonic and postnatal development , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[22]  F. Walsh,et al.  Cell adhesion molecules, second messengers and axonal growth , 1992, Current Opinion in Neurobiology.

[23]  P. Rakic,et al.  Selective role of N-type calcium channels in neuronal migration. , 1992, Science.

[24]  B. Kosofsky,et al.  Cocaine-induced disturbances of corticogenesis in the developing murine brain , 1992, Neuroscience Letters.

[25]  A. Kriegstein,et al.  Properties of amino acid neurotransmitter receptors of embryonic cortical neurons when activated by exogenous and endogenous agonists. , 1992, Journal of neurophysiology.

[26]  A. Schousboe,et al.  Regulatory role of astrocytes for neuronal biosynthesis and homeostasis of glutamate and GABA. , 1992, Progress in brain research.

[27]  G. Fishell,et al.  Astrotactin provides a receptor system for CNS neuronal migration. , 1991, Development.

[28]  S. Kater,et al.  Regulation of growth cone behavior by calcium , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[29]  W. Schlegel,et al.  Multiple elevations of cytosolic-free Ca2+ in human neutrophils: initiation by adherence receptors of the integrin family , 1991, The Journal of cell biology.

[30]  V. Gallo,et al.  Release of Endogenous and Newly Synthesized Glutamate and of Other Amino Acids Induced by Non‐N‐Methyl‐D‐Aspartate Receptor Activation in Cerebellar Granule Cell Cultures , 1991, Journal of neurochemistry.

[31]  S. Cull-Candy,et al.  Currents through single glutamate receptor channels in outside‐out patches from rat cerebellar granule cells. , 1991, The Journal of physiology.

[32]  A. Shemer,et al.  Role of High Affinity Serotonin Receptors in Neuronal Growth a , 1990, Annals of the New York Academy of Sciences.

[33]  N. Spitzer,et al.  Spontaneous calcium influx and its roles in differentiation of spinal neurons in culture. , 1990, Developmental biology.

[34]  P. Rakić,et al.  Axon overproduction and elimination in the corpus callosum of the developing rhesus monkey , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  M. Hatten,et al.  Riding the glial monorail: A common mechanism for glialguided neuronal migration in different regions of the developing mammalian brain , 1990, Trends in Neurosciences.

[36]  R Y Tsien,et al.  Calcium channels, stores, and oscillations. , 1990, Annual review of cell biology.

[37]  P. Forscher Calcium and polyphosphoinositide control of cytoskeletal dynamics , 1989, Trends in Neurosciences.

[38]  K. Lankford,et al.  Evidence that calcium may control neurite outgrowth by regulating the stability of actin filaments , 1989, The Journal of cell biology.

[39]  G White,et al.  Ethanol inhibits NMDA-activated ion current in hippocampal neurons. , 1989, Science.

[40]  P. Rakic Specification of cerebral cortical areas. , 1988, Science.

[41]  J. C. Edmondson,et al.  Astrotactin: a novel neuronal cell surface antigen that mediates neuron- astroglial interactions in cerebellar microcultures , 1988, The Journal of cell biology.

[42]  M. Schachner,et al.  Biochemical and functional characterization of a novel neuron-glia adhesion molecule that is involved in neuronal migration , 1987, The Journal of cell biology.

[43]  R. J. Miller,et al.  Multiple calcium channels and neuronal function. , 1987, Science.

[44]  J A Sullivan,et al.  Intracellular free calcium localization in neutrophils during phagocytosis. , 1985, Science.

[45]  S. Easter,et al.  The changing view of neural specificity. , 1985, Science.

[46]  P. Rakić,et al.  Differential distribution of intermembranous particles in the plasmalemma of the migrating cerebellar granule cells. , 1985, Brain research.

[47]  G. Edelman Modulation of cell adhesion during induction, histogenesis, and perinatal development of the nervous system. , 1984, Annual review of neuroscience.

[48]  P. Rakic Neuronal-glial interaction during brain development , 1981, Trends in Neurosciences.

[49]  P. Rakić,et al.  Mechanisms of cortical development: a view from mutations in mice. , 1978, Annual review of neuroscience.

[50]  P. Rakic Synaptic specificity in the cerebellar cortex: study of anomalous circuits induced by single gene mutations in mice. , 1976, Cold Spring Harbor symposia on quantitative biology.

[51]  S. Palay,et al.  Cerebellar Cortex: Cytology and Organization , 1974 .

[52]  P. Rakić,et al.  Sequence of developmental abnormalities leading to granule cell deficit in cerebellar cortex of weaver mutant mice , 1973, The Journal of comparative neurology.

[53]  P. Rakić,et al.  Neuronal migration, with special reference to developing human brain: a review. , 1973, Brain research.

[54]  V. Balcar,et al.  THE STRUCTURAL SPECIFICITY OF THE HIGH AFFINITY UPTAKE OF l‐GLUTAMATE AND l‐ASPARTATE BY RAT BRAIN SLICES , 1972, Journal of neurochemistry.

[55]  P. Rakić Mode of cell migration to the superficial layers of fetal monkey neocortex , 1972, The Journal of comparative neurology.

[56]  P. Rakić,et al.  Neuron‐glia relationship during granule cell migration in developing cerebellar cortex. A Golgi and electonmicroscopic study in Macacus rhesus , 1971, The Journal of comparative neurology.

[57]  S. Fujita QUANTITATIVE ANALYSIS OF CELL PROLIFERATION AND DIFFERENTIATION IN THE CORTEX OF THE POSTNATAL MOUSE CEREBELLUM , 1967, The Journal of cell biology.