4.3 Article

Distribution of metabotropic GABA receptor Subunits GABA(B1a/b) and GABA(B2) in the rat hippocampus during prenatal and postnatal development

Journal

HIPPOCAMPUS
Volume 14, Issue 7, Pages 836-848

Publisher

WILEY
DOI: 10.1002/hipo.10221

Keywords

GABA(B); immunohistochemistry; synapse; electron microscopy; development; light microscopy; inhibition

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Metabotropic gamma-aminobutyric acid receptors (GABA(B)) play modulatory roles in central synaptic transmission and are involved in controlling neuronal migration during development. We used immunohistochemical methods to elucidate the expression pattern as well as the cellular and the precise subcellular localization of the GABA(B1a/b) and GABA(B2) subunits in the rat hippocampus during prenatal and postnatal development. At the light microscopic level, both GABA(B1a/b) and GABA(B2) were expressed in the hippocampal primordium from embryonic day E14. During postnatal development, immunoreactivity for GABA(B1a/b) and GABA(B2) was distributed mainly in pyramidal cells, with discrete GABA(B1a/b)-immunopositive cell bodies of interneurons present throughout the hippocampus. Using double immunofluorescence, we demonstrated that during the second week of postnatal development, GABA(B1a/b) but not GABA(B2) was expressed in glial cells throughout the hippocampal formation. At the electron microscopic level, GABA(B1a/b) and GABA(B2) showed a similar distribution pattern during postnatal development. Thus, at all ages the two receptor subunits were located postsynaptically in dendritic spines and shafts at extrasynaptic and perisynaptic sites in both pyramidal and nonpyramidal cells. We further demonstrated that the two subunits were localized presynaptically along the extrasynaptic plasma membrane of axon terminals and along the presynaptic active zone in both asymmetrical and, to a lesser extent, symmetrical synapses. These results suggest that GABA(B) receptors are widely expressed in the hippocampus throughout development and that GABA(B1a/b) and GABA(B2) form both pre- and postsynaptic receptors. (C) 2004 Wiley-Liss, Inc.

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