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Short and Long Form γ2 Subunits of the GABAA/Benzodiazepine Receptors
Authors:Zafar U Khan  Antonia Gutiérrez  Angel L De Blas
Institution:Division of Molecular Biology and Biochemistry, School of Biological Sciences, University of Missouri-Kansas City, Kansas City, Missouri, U.S.A.
Abstract:Abstract: Three novel antisera to the γ2 subunit of the γ-aminobutyric acidA (GABAA) receptor/benzodiazepine receptor (GABAAR/BZDR) complex have been made. Anti-γ2S and anti-γ2L are specific antibodies to synthetic peptides that recognize the γ2S (short) and γ2L (long) forms, respectively, of the γ2 subunit. An antibody (anti-γ2IL2) to staphylococcal protein A fusion protein of the large intracellular loop (γ2IL) located between the putative transmembrane segments M3 and M4 of γ2S recognizes both γ2S and γ2L subunits. The antibodies immunoprecipitated both the solubilized and affinity-purified GABAAR/BZDR from rat and bovine brain. Immunoblots with membranes from rat brain cerebral cortex as well as with affinity-purified receptor from bovine cortex show that anti-γ2S and anti-γ2L recognize peptides of 45,000 and 47,000 Mr, respectively. Immunoprecipitation experiments indicate that γ2S is more prevalent in hippocampus, whereas γ2L is more abundant in cerebellum. Intermediate values for each form are found in the cerebral cortex. The results suggest that in the rat brain there is a considerable amount of colocalization of γ2S and γ2L in the same receptor complex. In the cerebral cortex, 15% of the BZDRs contain both γ2S and γ2L subunits and 41–48% of the γ2L subunit coexists with γ2S in the same receptor complex. In cerebellum, in 27% of the clonazepam-sensitive and 39% of the clonazepam-insensitive BZDRs the γ2S and γ2L coexist in the same receptor complex. The latter are presumably localized in granule cells and also contain α6. In addition, almost all (93%) the clonazepam-insensitive BZDRs that contain γ2L also contain a γ2S subunit in the same receptor complex. The most likely interpretation of the results is that there is an important population of granule cell receptors that contain α6, γ2S, and γ2L coexisting in the same receptor complex. Nevertheless, 31% of the cerebellar receptors that contain α6 subunit(s) have neither γ2S nor γ2L subunits. There are also species differences with respect to the relative abundance of γ2S and γ2L. These results might be relevant for understanding the molecular mechanisms underlying some of the GABAAR/BZDR-mediated effects of ethanol intoxication involving cerebellar granule cells.
Keywords:Antibody  γ-Aminobutyric acid receptor  Benzodiazepine receptor  γ2 Subunit  Ethanol
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