Khan Z U, Gutiérrez A, Miralles C P, De Blas A L
Division of Molecular Biology and Biochemistry, School of Biological Sciences, University of Missouri-Kansas City, MO 64110-2499, USA.
Neurochem Res. 1996 Feb;21(2):147-59. doi: 10.1007/BF02529132.
Subunit-specific antibodies to all the gamma subunit isoforms described in mammalian brain (gamma(1), gamma(2S), gamma(2L), and gamma(3) have been made. The proportion of GABA(A) receptors containing each gamma subunit isoform in various brain regions has been determined by quantitative immunoprecipitation. In all tested regions of the rat brain, the gamma(1) and gamma(3) subunits are present in considerable smaller proportion of GABA(A) receptor than the gamma(2) subunit. Immunocytochemistry shows that gamma(1) immunoreactivity concentrates in the stratum oriens and stratum radiatum of the CA1 region of the hippocampus. In the dentate gyrus, gamma(1) immunoreactivity concentrates on the outer 2/3 of the molecular layer coinciding with the localization of the axospinous synapses of the perforant pathway. In contrast, gamma(3) immunoreactivity concentrates on the basket cells and other GABAergic local circuit neurons of the hilus. These cells are also rich in gamma(2S). In the cerebellum, gamma(1)++ immunolabeling was localized on the Bergmann glia. The gamma(2S) and gamma(2L) subunits are differentially expressed in various brain regions. Thus the gamma(2S) is highly expressed in the olfactory bulb and hippocampus whereas the gamma(2L) is very abundant in inferior colliculus and cerebellum, particularly in Purkinje cells, as immunocytochemistry, in situ hybridization and immunoprecipitation techniques have revealed. The gamma(2S) and gamma(2L) coexist in some brain areas and cell types. Moreover, the gamma(2S) and gamma(2L) subunits can coexist in the same GABA(A) receptor pentamer. We have shown that this is the case in some GABA(A) receptors expressed in cerebellar granule cells. These GABA(A) receptors also have alpha and beta subunits forming the pentamer. Immunoblots have shown that the rat gamma(1), gamma(2S), gamma(2L) and gamma(3) subunits are peptides of 47, 45, 47 and 44 kDa respectively. Results also indicate that there are aging-related changes in the expression of the gamma(2S) and gamma(2L) subunits in various brain regions which suggest the existence of aging-related changes in the subunit composition of the GABA(A) receptors which in turn might lead to changes in receptor pharmacology. The results obtained with the various gamma subunit isoforms are discussed in terms of the high molecular and binding heterogeneity of the native GABA(A) receptors in brain.
已经制备出针对哺乳动物大脑中描述的所有γ亚基异构体(γ(1)、γ(2S)、γ(2L)和γ(3))的亚基特异性抗体。通过定量免疫沉淀法确定了不同脑区中含有每种γ亚基异构体的GABA(A)受体的比例。在大鼠大脑的所有测试区域中,γ(1)和γ(3)亚基在GABA(A)受体中的比例比γ(2)亚基小得多。免疫细胞化学显示,γ(1)免疫反应性集中在海马体CA1区的 Oriens 层和放射层。在齿状回中,γ(1)免疫反应性集中在分子层的外2/3,与穿通通路的轴棘突触定位一致。相比之下,γ(3)免疫反应性集中在齿状回的篮状细胞和其他GABA能局部回路神经元上。这些细胞也富含γ(2S)。在小脑中,γ(1)++免疫标记定位于伯格曼胶质细胞上。γ(2S)和γ(2L)亚基在不同脑区中差异表达。因此,γ(2S)在嗅球和海马体中高度表达,而γ(2L)在下丘和小脑中非常丰富,特别是在浦肯野细胞中,免疫细胞化学、原位杂交和免疫沉淀技术已经揭示了这一点。γ(2S)和γ(2L)在一些脑区和细胞类型中共存。此外,γ(2S)和γ(2L)亚基可以共存于同一个GABA(A)受体五聚体中。我们已经证明在小脑颗粒细胞中表达的一些GABA(A)受体就是这种情况。这些GABA(A)受体也有形成五聚体的α和β亚基。免疫印迹显示,大鼠γ(1)、γ(2S)、γ(2L)和γ(3)亚基分别是47、45、47和44 kDa的肽。结果还表明,不同脑区中γ(2S)和γ(2L)亚基的表达存在与衰老相关的变化,这表明GABA(A)受体的亚基组成存在与衰老相关的变化,进而可能导致受体药理学的变化。根据大脑中天然GABA(A)受体的高分子和结合异质性,讨论了用各种γ亚基异构体获得的结果。