Brecha N C, Weigmann C
Department of Anatomy and Cell Biology, VA/UCLA Gastroenteric Biology Center.
J Comp Neurol. 1994 Jul 22;345(4):602-11. doi: 10.1002/cne.903450410.
Gamma-aminobutyric acid (GABA) plasma membrane transporters influence synaptic transmission by high-affinity, Na(+)-dependent transport processes. The cDNA clone, GAT-1, encodes a high-affinity Na(+)- and Cl(-)-dependent GABA plasma membrane transporter, which has kinetic and pharmacological properties similar to those of high-affinity GABA uptake systems associated with neurons. The present study evaluates the distribution and cellular localization of this putative neuronal GABA transporter by RNA blot hybridization and in situ hybridization histochemistry in the rat retina. Northern blot hybridization analysis of total retinal and cerebellar RNA extracts demonstrated a single band of hybridization at 4.2 kilobases. GABA transporter mRNA is expressed by numerous cells that are distributed to the proximal inner nuclear layer and the ganglion cell layer and by a few cells located in the inner plexiform layer. Double label studies combining the retrograde transport of the fluorescent dye Fluorogold from the superior colliculus to identify ganglion cells and in situ hybridization histochemistry demonstrated that most GAT-1 mRNA-containing cells in the ganglion cell layer are displaced amacrine cells, although some ganglion cells containing GAT-1 mRNA were visualized. In freshly dissociated retinal cell preparations, the GAT-1 RNA signal is strong in neurons and weak to moderate in specialized glial cells called Müller cells. Müller cells were identified by both their morphology and the presence of the selective Müller cell marker cellular retinaldehyde-binding protein. Only background labeling is seen with the sense GAT-1 RNA probe in both tissue sections and dissociated retinal cell preparations. These findings demonstrate that GAT-1 mRNA is expressed in both the retina and brain. In the retina, this transporter is predominantly localized to amacrine, displaced amacrine and interplexiform cells, and some ganglion cells. This transporter mRNA is also expressed by Müller cells but at a lower level than by neurons. These observations indicate that GABA transport by GAT-1 plasma membrane transporters in the retina is mediated by both neurons and glia cells.
γ-氨基丁酸(GABA)质膜转运体通过高亲和力、依赖钠离子的转运过程影响突触传递。cDNA克隆GAT-1编码一种高亲和力的、依赖钠离子和氯离子的GABA质膜转运体,其动力学和药理学特性与神经元相关的高亲和力GABA摄取系统相似。本研究通过RNA印迹杂交和原位杂交组织化学方法评估了这种假定的神经元GABA转运体在大鼠视网膜中的分布和细胞定位。对视网膜和小脑总RNA提取物的Northern印迹杂交分析显示,在4.2千碱基处有一条单一的杂交带。GABA转运体mRNA由分布于近端内核层和神经节细胞层的众多细胞以及位于内网状层的少数细胞表达。结合从上丘逆行转运荧光染料Fluorogold以识别神经节细胞的双重标记研究和原位杂交组织化学表明,神经节细胞层中大多数含有GAT-1 mRNA的细胞是移位无长突细胞,尽管也观察到一些含有GAT-1 mRNA的神经节细胞。在新鲜分离的视网膜细胞制剂中,GAT-1 RNA信号在神经元中很强,而在一种称为Müller细胞的特殊神经胶质细胞中较弱至中等强度。通过形态学和选择性Müller细胞标记物细胞视黄醛结合蛋白的存在来鉴定Müller细胞。在组织切片和分离的视网膜细胞制剂中,正义GAT-1 RNA探针仅显示背景标记。这些发现表明GAT-1 mRNA在视网膜和脑中均有表达。在视网膜中,这种转运体主要定位于无长突细胞、移位无长突细胞和网间细胞以及一些神经节细胞。这种转运体mRNA也由Müller细胞表达,但水平低于神经元。这些观察结果表明,视网膜中GAT-1质膜转运体介导的GABA转运是由神经元和神经胶质细胞共同介导的。