Literature DB >> 9182849

Developmental expression of GABA(A) receptor subunit and GAD genes in mouse somatosensory barrel cortex.

P Golshani1, H Truong, E G Jones.   

Abstract

In situ hybridization histochemistry with radioactive cRNA probes was used to study patterns of gene expression for alpha1, alpha2, alpha4, alpha5, beta1, beta2, and gamma2 subunit mRNAs of typeAgamma aminobutyric acid (GABA(A)) receptors and for 67-kDa glutamic acid decarboxylase (GAD67) mRNA in mouse barrel cortex during the period (postnatal days 1-12; P1-P12) when thalamocortical innervation of layer IV barrels is occurring. The alpha1, beta2, and gamma2 subunit mRNAs increased substantially with age, especially in layers V and VI, and throughout the period studied, invariably had the same laminar-specific patterns of expression. All three mRNAs were highly expressed in the dense cortical plate at P1. In layer IV after differentiation of barrels, they were expressed in cells of both barrel walls and hollows but especially in the walls. The alpha2, alpha4, alpha5, and beta1 subunit mRNAs were expressed at lower levels and had different laminar patterns of distribution; alpha2 and alpha4 showed switches between layers over time; alpha5 was invariably associated with the subplate or its derivative, beta1 with layer IV. Levels of alpha2 mRNA did not change over time; alpha4 and beta1 mRNAs increased and alpha5 decreased. GAD67 mRNA was highest in layer I at P1 and progressively increased in other layers. These results suggest that postnatal development of GABA(A) receptors is mainly directed at the production of receptors assembled from alpha1, beta2, and gamma2 subunits, with beta1 contributing in layer IV. Other subunits may be associated with receptors involved in trophic actions of GABA during development and may give GABA(A) receptor-mediated responses in the developing cortex their particular physiological profile.

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Year:  1997        PMID: 9182849     DOI: 10.1002/(sici)1096-9861(19970630)383:2<199::aid-cne7>3.0.co;2-w

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


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