Nusser Z, Roberts J D, Baude A, Richards J G, Sieghart W, Somogyi P
Medical Research Council, Anatomical Neuropharmacology Unit, University of Oxford, UK.
Eur J Neurosci. 1995 Apr 1;7(4):630-46. doi: 10.1111/j.1460-9568.1995.tb00667.x.
Dentate granule cells receive spatially segregated GABAergic innervation from at least five types of local circuit neurons, and express mRNA for at least 11 subunits of the GABAA receptor. At most two to four different subunits are required to make a functional pentamer, raising the possibility that cells have on their surface several types of GABAA receptor channel, which may not be uniformly distributed. In order to establish the subcellular location of GABAA receptors on different parts of dentate neurons, the distribution of immunoreactivity for the alpha 1 and beta 2/3 subunits of the receptor was studied using high-resolution immunocytochemistry. Light microscopic immunoperoxidase reactions revealed strong GABAA receptor immunoreactivity in the molecular layer of the dentate gyrus. Pre-embedding immunogold localization of the alpha 1 and beta 2/3 subunits consistently showed extrasynaptic location of the GABAA receptor on the somatic, dendritic and axon initial segment membrane of granule cells, but failed to show receptors in synaptic junctions. Using a postembedding immunogold technique on freeze-substituted, Lowicryl-embedded tissue, synaptic enrichment of immunoreactivity for these subunits was found on both granule and non-principal cells. Only the postembedding immunogold method is suitable for revealing relative differences in receptor density at the subcellular level, giving approximately 20 nm resolution. The immunolabelling for GABAA receptor occupied the whole width of synaptic junctions, with a sharp decrease in labelling at the edge of the synaptic membrane specialization. Both subunits have been localized in the synaptic junctions between basket cell terminals and somata, and between axo-axonic cell terminals and axon initial segments of granule cells, with no qualitative difference in labelling. Receptor-immunopositive synapses were found at all depths of the molecular layer. Some of the boutons forming these dendritic synapses have been shown to contain GABA, providing evidence that some of the GABAergic cells that terminate only on the dendrites of granule cells also act through GABAA receptors. Double immunolabelling experiments demonstrated that a population of GABA-immunopositive neurons expresses a higher density of immunoreactive GABAA receptor on their surface than principal cells. Interneurons were found to receive GABAA receptor-positive synapses on their dendrites in the hilus, molecular and granule cell layers. Receptor-immunopositive synapses were also present throughout the hilus on presumed mossy cells. The results demonstrate that both granule cells and interneurons exhibit a compartmentalized distribution of the GABAA receptor on their surface, the postjunctional membrane to GABAergic terminals having the highest concentration of receptor.(ABSTRACT TRUNCATED AT 400 WORDS)
齿状颗粒细胞从至少五种类型的局部回路神经元接收空间上分离的GABA能神经支配,并表达GABAA受体至少11个亚基的mRNA。形成一个功能性五聚体最多需要两到四个不同的亚基,这增加了细胞表面可能有几种类型的GABAA受体通道且分布不均一的可能性。为了确定GABAA受体在齿状神经元不同部位的亚细胞定位,使用高分辨率免疫细胞化学研究了受体α1和β2/3亚基的免疫反应性分布。光学显微镜免疫过氧化物酶反应显示齿状回分子层有强烈的GABAA受体免疫反应性。α1和β2/3亚基的包埋前免疫金定位始终显示GABAA受体在颗粒细胞的体细胞、树突和轴突起始段膜上位于突触外,但在突触连接处未显示有受体。在冷冻替代、Lowicryl包埋的组织上使用包埋后免疫金技术,发现这些亚基的免疫反应性在颗粒细胞和非主要细胞上都有突触富集。只有包埋后免疫金方法适用于揭示亚细胞水平上受体密度的相对差异,分辨率约为20纳米。GABAA受体的免疫标记占据了突触连接的整个宽度,在突触膜特化边缘标记急剧减少。两个亚基都已定位在篮状细胞终末与体细胞之间以及颗粒细胞的轴-轴突细胞终末与轴突起始段之间的突触连接处,标记没有质的差异。在分子层的所有深度都发现了受体免疫阳性突触。形成这些树突突触的一些轴突终末已被证明含有GABA,这提供了证据表明一些仅终止于颗粒细胞树突上的GABA能细胞也通过GABAA受体起作用。双重免疫标记实验表明,一群GABA免疫阳性神经元在其表面表达的免疫反应性GABAA受体密度高于主要细胞。在门区、分子层和颗粒细胞层的中间神经元的树突上发现有GABAA受体阳性突触。在整个门区假定的苔藓细胞上也有受体免疫阳性突触。结果表明,颗粒细胞和中间神经元在其表面都表现出GABAA受体的分区分布,GABA能终末的突触后膜受体浓度最高。(摘要截断于400字)