Literature DB >> 7891188

Complementary expressions of transcripts encoding GAD67 and GABAA receptor alpha 4, beta 1, and gamma 1 subunits in the proliferative zone of the embryonic rat central nervous system.

W Ma1, J L Barker.   

Abstract

The developmental stage at which nerve cells initially express specific neurotransmitters and their corresponding receptors remains elusive. In the present study, the distribution patterns of transcripts for the GABA-synthesizing enzyme, glutamate decarboxylase (GAD67), and specific GABAA receptor subunits were examined in the proliferative zone of the rat central nervous system using in situ hybridization. In order to define the DNA synthetic zone of the germinal matrix, tissue sections were taken from embryos whose mothers had been injected with 5-bromo-2'-deoxyuridine (BrdU) and had survived for 1 hr. BrdU immunocytochemistry was used to locate the relative position of BrdU-immunoreactive nuclei within the ventricular zone (VZ). At embryonic day (E) 15 in the alar plate of the lumbar spinal cord, and at E17 and E20 in the dorsomedial sector of the neocortex, densely packed BrdU-immunoreactive nuclei were consistently detected in lateral portions of the inner half of the germinal matrix, indicating that the inner half of the germinal matrix corresponded to the VZ, while the outer half corresponded to the transitional (TZ) or subventricular zone (SV). In situ hybridization in tissue sections adjacent to BrdU-immunoreacted ones showed that the transcripts for GABAA receptor alpha 3, beta 3, and gamma 2 subunits were found exclusively in the mantle zone, while those for alpha 4, beta 1, and gamma 1 subunits were predominantly detected in the inner half of the germinal matrix (i.e., VZ). Furthermore, in the E15 germinal matrix of the lumbar spinal cord, cells exhibiting alpha 4 subunit mRNA were much more abundant in the receding intermediate plate, which contains mostly postmitotic cells, than in the alar plate comprised of many DNA-synthesizing cells, strongly suggesting that only those cells completing final cell division expressed the subunit mRNAs. In clear contrast, GAD67 mRNA was abundant in the outer half of the germinal matrix (i.e., TZ or SV), and in the intermediate zone as well. Immunocytochemical staining of E17 neocortex with anti-GABA antibody revealed a well defined band of GABA-immunoreactive cells and processes in the SV and occasional positive cells in the VZ. It appears that cells in the proliferative zone may express GABA at the migratory stage, whereas cells in the VZ may express mRNAs for GABAA receptor alpha 4, beta 1, and gamma 1 subunits at the premigratory stage, just after completing cell division.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1995        PMID: 7891188      PMCID: PMC6578170     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  24 in total

1.  GABA expression dominates neuronal lineage progression in the embryonic rat neocortex and facilitates neurite outgrowth via GABA(A) autoreceptor/Cl- channels.

Authors:  D Maric; Q Y Liu; I Maric; S Chaudry; Y H Chang; S V Smith; W Sieghart; J M Fritschy; J L Barker
Journal:  J Neurosci       Date:  2001-04-01       Impact factor: 6.167

Review 2.  GABAA receptors, anesthetics and anticonvulsants in brain development.

Authors:  Oliver Henschel; Keith E Gipson; Angelique Bordey
Journal:  CNS Neurol Disord Drug Targets       Date:  2008-04       Impact factor: 4.388

3.  Multimodal Single-Cell Analysis Reveals Physiological Maturation in the Developing Human Neocortex.

Authors:  Simone Mayer; Jiadong Chen; Dmitry Velmeshev; Andreas Mayer; Ugomma C Eze; Aparna Bhaduri; Carlos E Cunha; Diane Jung; Arpana Arjun; Emmy Li; Beatriz Alvarado; Shaohui Wang; Nils Lovegren; Michael L Gonzales; Lukasz Szpankowski; Anne Leyrat; Jay A A West; Georgia Panagiotakos; Arturo Alvarez-Buylla; Mercedes F Paredes; Tomasz J Nowakowski; Alex A Pollen; Arnold R Kriegstein
Journal:  Neuron       Date:  2019-02-12       Impact factor: 17.173

4.  Cleft palate and decreased brain gamma-aminobutyric acid in mice lacking the 67-kDa isoform of glutamic acid decarboxylase.

Authors:  H Asada; Y Kawamura; K Maruyama; H Kume; R G Ding; N Kanbara; H Kuzume; M Sanbo; T Yagi; K Obata
Journal:  Proc Natl Acad Sci U S A       Date:  1997-06-10       Impact factor: 11.205

5.  GABAA receptor subunit composition and functional properties of Cl- channels with differential sensitivity to zolpidem in embryonic rat hippocampal cells.

Authors:  D Maric; I Maric; X Wen; J M Fritschy; W Sieghart; J L Barker; R Serafini
Journal:  J Neurosci       Date:  1999-06-15       Impact factor: 6.167

Review 6.  GABAergic Regulation of Adult Hippocampal Neurogenesis.

Authors:  Mirjam Sibbe; Akos Kulik
Journal:  Mol Neurobiol       Date:  2016-09-06       Impact factor: 5.590

7.  GABAA receptors mediate trophic effects of GABA on embryonic brainstem monoamine neurons in vitro.

Authors:  J Liu; A L Morrow; L Devaud; D R Grayson; J M Lauder
Journal:  J Neurosci       Date:  1997-04-01       Impact factor: 6.167

8.  Cloning and characterization of GABAA α subunits and GABAB subunits in Xenopus laevis during development.

Authors:  Gwendolyn E Kaeser; Brian A Rabe; Margaret S Saha
Journal:  Dev Dyn       Date:  2011-03-07       Impact factor: 3.780

9.  Autocrine/paracrine activation of the GABA(A) receptor inhibits the proliferation of neurogenic polysialylated neural cell adhesion molecule-positive (PSA-NCAM+) precursor cells from postnatal striatum.

Authors:  Laurent Nguyen; Brigitte Malgrange; Ingrid Breuskin; Lucien Bettendorff; Gustave Moonen; Shibeshih Belachew; Jean-Michel Rigo
Journal:  J Neurosci       Date:  2003-04-15       Impact factor: 6.167

Review 10.  Neurosteroid regulation of central nervous system development.

Authors:  Synthia H Mellon
Journal:  Pharmacol Ther       Date:  2007-06-16       Impact factor: 12.310

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