Temporal modulation of GABAA receptor subunit gene expression in developing monkey cerebral cortex

In situ hybridization histochemistry was used to examine the expression of 10 GABA(A) receptor messenger RNAs corresponding to the alpha1-alpha5, beta1-beta3, gamma1 and gamma2 subunits in primary somatosensory and visual areas of macaque monkey cerebral cortex from embryonic day (E) 125 to postnatal day (P) 125. Results were compared with expression patterns in adults. In the sensorimotor cortex at E125, overall levels of all subunit transcripts were low. At E137, there was a major lamina-specific increase in all subunit messenger RNAs except gamma1. For alpha1, alpha2, alpha4, beta2, beta3 and gamma2 subunit transcripts, this increase was highest in areas 3a and 3b, particularly in layers III/IV and VI. Postnatally, there were significant decreases in all transcripts. Alpha1, alpha5, beta2 and gamma2 subunit transcripts, while still at significantly lower levels than at E137, remained expressed at levels higher than other transcripts. Unlike in rodents, there was no obvious "switch" in the major subunits expressed in fetal and adult cortex, alpha1, alpha5, beta2 and gamma2 remaining highest throughout. In area 17, the most prominently expressed subunits at earliest ages were alpha2, alpha5, beta1, beta2, beta3 and gamma2, especially in layers II/III and VI. At E150, expression for alpha2, alpha3, beta1 and beta3 subunit transcripts in these layers decreased, but levels for alpha1, alpha4, alpha5, beta2, gamma1 and gamma2 transcripts increased, particularly within layer IV. The increase at E150 was particularly marked for alpha5 transcripts, which were expressed at levels more than four times those of other transcripts. Alpha1, beta2 and gamma2 remain highest into aduthood. Fetal area 17 displayed lamina-specific patterns of expression not found in adult animals. In particular, alpha3 messenger RNAs were present in layer IVA and gamma1 transcripts were present in layer IVC at E150, despite a lack of expression in these layers in the adult. These data demonstrate increased expression of GABA(A) receptors during the period of establishment of thalamocortical and intracortical connections, and a temporal regulation that may be associated with the period of developmental plasticity.

[1]  J. Wolff Evidence for a dual role of GABA as a synaptic transmitter and a promoter of synaptogenesis. , 1981, Advances in biochemical psychopharmacology.

[2]  M. Stryker,et al.  Binocular impulse blockade prevents the formation of ocular dominance columns in cat visual cortex , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[3]  E. G. Jones,et al.  Organized growth of thalamocortical axons from the deep tier of terminations into layer IV of developing mouse barrel cortex , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[4]  W Wisden,et al.  The distribution of 13 GABAA receptor subunit mRNAs in the rat brain. I. Telencephalon, diencephalon, mesencephalon , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[5]  E. G. Jones,et al.  Reduction in number of immunostained GABAergic neurones in deprived-eye dominance columns of monkey area 17 , 1986, Nature.

[6]  D. Hubel,et al.  Laminar and columnar distribution of geniculo‐cortical fibers in the macaque monkey , 1972, The Journal of comparative neurology.

[7]  H. Burton,et al.  Bicuculline-induced alterations in neuronal responses to controlled tactile stimuli in the second somatosensory cortex of the cat: a microiontophoretic study. , 1986, Somatosensory research.

[8]  P. Golshani,et al.  Developmental expression of GABAA receptor subunit and GAD genes in mouse somatosensory barrel cortex , 1997, The Journal of comparative neurology.

[9]  R. Dykes,et al.  Receptive field size for certain neurons in primary somatosensory cortex is determined by GABA-mediated intracortical inhibition , 1983, Brain Research.

[10]  A. Hendrickson,et al.  Coincidental appearance of the α1 subunit of the gaba-a receptor and the type ibenzodiazepine receptor near birth in macaque monkey visual cortex , 1994, International Journal of Developmental Neuroscience.

[11]  P. Seeburg,et al.  Importance of a novel GABAA receptor subunit for benzodiazepine pharmacology , 1989, Nature.

[12]  J. Hornung,et al.  Developmental profile of GABAA‐receptors in the marmoset monkey: Expression of distinct subtypes in pre‐ and postnatal brain , 1996, The Journal of comparative neurology.

[13]  C. Gambarana,et al.  Region-specific expression of messenger RNAs encoding GABAa receptor subunits in the developing rat brain , 1991, Neuroscience.

[14]  P. Rakić,et al.  Neurotransmitter receptors in the proliferative zones of the developing primate occipital lobe , 1995, The Journal of comparative neurology.

[15]  P S Goldman-Rakic,et al.  Transient cholinesterase staining in the mediodorsal nucleus of the thalamus and its connections in the developing human and monkey brain , 1983, The Journal of comparative neurology.

[16]  A. Trzeciak,et al.  GABAA receptors display association of gamma 2-subunit with alpha 1- and beta 2/3-subunits. , 1991, The Journal of biological chemistry.

[17]  M. Huntsman,et al.  Nucleus-Specific Expression of GABAA Receptor Subunit mRNAs in Monkey Thalamus , 1996, The Journal of Neuroscience.

[18]  A. Agmon,et al.  NMDA receptor-mediated currents are prominent in the thalamocortical synaptic response before maturation of inhibition. , 1992, Journal of neurophysiology.

[19]  J. Barker,et al.  Transient expression of GABA immunoreactivity in the developing rat spinal cord , 1992, The Journal of comparative neurology.

[20]  H. Tamura,et al.  Inhibition contributes to orientation selectivity in visual cortex of cat , 1988, Nature.

[21]  Rafael Yuste,et al.  Control of postsynaptic Ca2+ influx in developing neocortex by excitatory and inhibitory neurotransmitters , 1991, Neuron.

[22]  P. Rakic Prenatal genesis of connections subserving ocular dominance in the rhesus monkey , 1976, Nature.

[23]  A. Schousboe,et al.  Effect of Repeated Treatment with a γ‐Aminobutyric Acid Receptor Agonist on Postnatal Neural Development in Rats , 1987, Journal of neurochemistry.

[24]  S. Smith,et al.  GABAergic cells and signals appear together in the early post-mitotic period of telencephalic and striatal development. , 1993, Brain research. Developmental brain research.

[25]  E. G. Jones,et al.  Lamination and differential distribution of thalamic afferents within the sensory‐motor cortex of the squirrel monkey , 1975, The Journal of comparative neurology.

[26]  Xavier Leinekugel,et al.  Ca2+ Oscillations Mediated by the Synergistic Excitatory Actions of GABAA and NMDA Receptors in the Neonatal Hippocampus , 1997, Neuron.

[27]  A. Kriegstein,et al.  GABA and glutamate depolarize cortical progenitor cells and inhibit DNA synthesis , 1995, Neuron.

[28]  E. G. Jones,et al.  Distribution and plasticity of immunocytochemically localized GABAA receptors in adult monkey visual cortex , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[29]  M. Huntsman,et al.  Lamina-specific expression and activity-dependent regulation of seven GABAA receptor subunit mRNAs in monkey visual cortex , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[30]  P. Rakić,et al.  Development of prestriate visual projections in the monkey and human fetal cerebrum revealed by transient cholinesterase staining , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[31]  P S Goldman-Rakic,et al.  Synchronized overproduction of neurotransmitter receptors in diverse regions of the primate cerebral cortex. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[32]  S. B. Kater,et al.  Neuronal growth cone as an integrator of complex environmental information. , 1990, Cold Spring Harbor symposia on quantitative biology.

[33]  H. Mohler,et al.  GABAA receptor subunit immunoreactivity in primate visual cortex: distribution in macaques and humans and regulation by visual input in adulthood , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[34]  M. Tohyama,et al.  GABAA Receptor subunit messenger RNAs show differential expression during cortical development in the rat brain , 1992, Neuroscience.

[35]  A. N. van den Pol,et al.  GABA neurotransmission in the hypothalamus: developmental reversal from Ca2+ elevating to depressing , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[36]  C. K. Mitchell,et al.  GABA and GABA-A receptors are maximally expressed in association with cone synaptogenesis in neonatal rabbit retina. , 1996, Brain research. Developmental brain research.

[37]  A. Goldstein,et al.  Levels of immunoreactive dynorphin in brain and pituitary of Brattleboro rats , 1980, Neuroscience Letters.

[38]  T. Powell,et al.  Connexions of the somatic sensory cortex of the rhesus monkey. 3. Thalamic connexions. , 1970, Brain : a journal of neurology.

[39]  Pasko Rakic,et al.  Cytology and time of origin of interstitial neurons in the white matter in infant and adult human and monkey telencephalon , 1980, Journal of neurocytology.

[40]  J. Paysan,et al.  Switch in the expression of rat GABAA-receptor subtypes during postnatal development: an immunohistochemical study , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[41]  S. Wise,et al.  Prenatal development of sensorimotor cortical projections in cats , 1977, Brain Research.

[42]  B. Sakmann,et al.  Functional properties of recombinant rat GABAA receptors depend upon subunit composition , 1990, Neuron.

[43]  H. Killackey,et al.  Process elimination underlies ontogenetic change in the distribution of callosal projection neurons in the postcentral gyrus of the fetal rhesus monkey. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[44]  E. G. Jones,et al.  The organization and postnatal development of the commissural projection of the rat somatic sensory cortex , 1976, The Journal of comparative neurology.

[45]  M. Huntsman,et al.  Laminar patterns of expression of GABAA receptor subunit mRNAs in monkey sensory motor cortex , 1995, The Journal of comparative neurology.

[46]  C. Gilbert,et al.  Generation of end-inhibition in the visual cortex via interlaminar connections , 1986, Nature.

[47]  R. Macdonald,et al.  Assembly of GABAA receptor subunits: alpha 1 beta 1 and alpha 1 beta 1 gamma 2S subunits produce unique ion channels with dissimilar single- channel properties , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[48]  M. Ogren,et al.  The neurological organization of pathways between the dorsal lateral geniculate nucleus and visual cortex in old world and new world primates , 1978, The Journal of comparative neurology.

[49]  J. Kaas,et al.  The relay of ipsilateral and contralateral retinal input from the lateral geniculate nucleus to striate cortex in the owl monkey: a transneuronal transport study , 1976, Brain Research.

[50]  H. Killackey,et al.  Ontogenetic change in the distribution of callosal projection neurons in the postcentral gyrus of the fetal rhesus monkey , 1986, The Journal of comparative neurology.

[51]  M. Cynader,et al.  Pre- and postnatal development of GABA receptors in Macaca monkey visual cortex , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[52]  T. Powell,et al.  Connexions of the somatic sensory cortex of the rhesus monkey. II. Contralateral cortical connexions. , 1969, Brain : a journal of neurology.

[53]  B. Connors,et al.  Two inhibitory postsynaptic potentials, and GABAA and GABAB receptor‐mediated responses in neocortex of rat and cat. , 1988, The Journal of physiology.

[54]  A. Sillito The contribution of inhibitory mechanisms to the receptive field properties of neurones in the striate cortex of the cat. , 1975, The Journal of physiology.

[55]  U. Eysel,et al.  GABA-induced inactivation of functionally characterized sites in cat visual cortex (area 18): effects on orientation tuning , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[56]  Gerhard Trube,et al.  The effect of subunit composition of rat brain GABAA receptors on channel function , 1990, Neuron.

[57]  D. Hubel,et al.  Thalamic inputs to cytochrome oxidase-rich regions in monkey visual cortex. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[58]  P. Rakić,et al.  Expression of GABA and GABAa receptors by neurons of the subplate zone in developing primate occipital cortex: Evidence for transient local circuits , 1992, The Journal of comparative neurology.

[59]  C. Shatz,et al.  Synaptic Activity and the Construction of Cortical Circuits , 1996, Science.

[60]  R. Olsen,et al.  A novel α subunit in rat brain GABAA receptors , 1989, Neuron.

[61]  S P Wise,et al.  Developmental studies of thalamocortical and commissural connections in the rat somatic sensory cortex , 1978, The Journal of comparative neurology.

[62]  Y. Ben-Ari,et al.  Involvement of GABAA receptors in the outgrowth of cultured hippocampal neurons , 1993, Neuroscience Letters.

[63]  P. Seeburg,et al.  GABAA receptor channels: from subunits to functional entities , 1992, Current Opinion in Neurobiology.

[64]  E. Sigel,et al.  Functional characteristics and sites of gene expression of the alpha 1, beta 1, gamma 2-isoform of the rat GABAA receptor , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[65]  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.

[66]  H. Killackey,et al.  Temporal sequence of neurotransmitter expression by developing neurons of fetal monkey visual cortex. , 1988, Brain research.

[67]  S. Hendry,et al.  Activity-dependent regulation of GABA expression in the visual cortex of adult monkeys , 1988, Neuron.

[68]  J. Barker,et al.  Differential and transient expression of GABAA receptor alpha-subunit mRNAs in the developing rat CNS , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[69]  A. Kriegstein,et al.  Excitatory GABA Responses in Embryonic and Neonatal Cortical Slices Demonstrated by Gramicidin Perforated-Patch Recordings and Calcium Imaging , 1996, The Journal of Neuroscience.

[70]  C. Shatz Impulse activity and the patterning of connections during cns development , 1990, Neuron.

[71]  P. Malherbe,et al.  Comparative molecular neuroanatomy of cloned GABAA receptor subunits in the rat CNS , 1992, The Journal of comparative neurology.

[72]  B. Sakmann,et al.  Mechanism of anion permeation through channels gated by glycine and gamma‐aminobutyric acid in mouse cultured spinal neurones. , 1987, The Journal of physiology.

[73]  A. N. van den Pol,et al.  Growth cone calcium elevation by GABA , 1996, The Journal of comparative neurology.

[74]  L. Mahan,et al.  Co-existent expression of GABAA receptorβ2, β3 andγ2 subunit messenger RNAs during embryogenesis and early postnatal development of the rat central nervous system , 1993, Neuroscience.

[75]  A. Agmon,et al.  Functional GABAergic Synaptic Connection in Neonatal Mouse Barrel Cortex , 1996, The Journal of Neuroscience.

[76]  G. W. Huntley,et al.  The emergence of architectonic field structure and areal borders in developing monkey sensorimotor cortex , 1991, Neuroscience.

[77]  J. Barker,et al.  GABA stimulates chemotaxis and chemokinesis of embryonic cortical neurons via calcium-dependent mechanisms , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[78]  D. Hubel,et al.  The development of ocular dominance columns in normal and visually deprived monkeys , 1980, The Journal of comparative neurology.

[79]  E G Jones,et al.  Inhibitory synaptogenesis in mouse somatosensory cortex. , 1997, Cerebral cortex.

[80]  T. Tsumoto,et al.  Intracellular calcium increase induced by GABA in visual cortex of fetal and neonatal rats and its disappearance with development , 1994, Neuroscience Research.

[81]  H. Burton,et al.  Areal differences in the laminar distribution of thalamic afferents in cortical fields of the insular, parietal and temporal regions of primates , 1976, The Journal of comparative neurology.

[82]  M. Huntsman,et al.  Expression of α3, β3 and γ1 GABAA receptor subunit messenger RNAs in visual cortex and lateral geniculate nucleus of normal and monocularly deprived monkeys , 1998, Neuroscience.