Cuenca Nicolas, Deng Ping, Linberg Ken A, Lewis Geoffrey P, Fisher Steven K, Kolb Helga
Department of Biotechnology, University of Alicante, Alicante, Spain.
J Neurocytol. 2002 Sep-Nov;31(8-9):649-66. doi: 10.1023/a:1025791512555.
Ground squirrel retinas were immunostained with antibodies against calcium binding proteins (CBPs) and classical neurotransmitters in order to describe neuronal phenotypes in a diurnal mammalian retina and to then compare these neurons with those of more commonly studied nocturnal retinas like cats' and rabbits'. Double immunostained tissue was examined by confocal microscopy using antibodies against the following: rhodopsin and the CBPs, calbindin, calretinin, parvalbumin, calmodulin and recoverin (CB, CR, PV, CM, RV), glycine, GABA, choline acetyltransferase (CHAT) and tyrosine hydroxylase (TOH). In ground squirrel retina, the traditional cholinergic mirror symmetric amacrine cells colocalize CHAT with PV and GABA and faintly with glycine. A second cholinergic amacrine cell type colocalizes glycine alone. CR is found in at least 3 different amacrine cell types. The CR-immunoreactive (IR) cell population is a mixture of glycinergic and GABAergic types. The dopamine cell type IR to tyrosine hydroxylase has the typical morphology of a wide field cell with dendrites in S1 but the "rings" seen in cat or rabbit retina are not as numerous. TOH-IR amacrine cells send large club-shaped processes to the outer plexiform layer. CB and CR are in bipolar cells, A- and B-type horizontal cells and several amacrine cell types. Anti-rhodopsin labels the low density rod photoreceptor population in this species. Anti-recoverin labels cones and some bipolar cells while PKC is found in several different bipolar cell types. One ganglion cell with dendritic branching in S3 is strongly CR-IR. We find no evidence for an AII amacrine cell in the ground squirrel, with either anti-CR or anti-PV. An amacrine cell with similarity to the DAP1-3 cell of rabbit is CR-IR and glycine-IR. We discuss this labeling pattern in relationship to other mammalian species. The differences in staining patterns and phenotypes revealed suggest a functional diversity in the populations of amacrine cells according to whether the retinas are rod or cone dominated.
为了描述昼行性哺乳动物视网膜中的神经元表型,并将这些神经元与猫和兔子等更常研究的夜行性视网膜中的神经元进行比较,地松鼠视网膜用针对钙结合蛋白(CBPs)和经典神经递质的抗体进行免疫染色。使用针对以下物质的抗体通过共聚焦显微镜检查双重免疫染色的组织:视紫红质和CBPs、钙结合蛋白、钙视网膜蛋白、小白蛋白、钙调蛋白和恢复蛋白(CB、CR、PV、CM、RV)、甘氨酸、GABA、胆碱乙酰转移酶(CHAT)和酪氨酸羟化酶(TOH)。在地松鼠视网膜中,传统的胆碱能镜像对称无长突细胞使CHAT与PV和GABA共定位,并与甘氨酸微弱共定位。第二种胆碱能无长突细胞类型仅使甘氨酸共定位。CR存在于至少3种不同的无长突细胞类型中。CR免疫反应性(IR)细胞群体是甘氨酸能和GABA能类型的混合物。对酪氨酸羟化酶呈IR的多巴胺细胞类型具有宽视野细胞的典型形态,其树突位于S1,但在猫或兔子视网膜中看到的“环”数量没有那么多。TOH-IR无长突细胞向外网状层发送大的棒状突起。CB和CR存在于双极细胞、A 型和 B 型水平细胞以及几种无长突细胞类型中。抗视紫红质标记该物种中低密度的视杆光感受器群体。抗恢复蛋白标记视锥细胞和一些双极细胞,而PKC存在于几种不同的双极细胞类型中。一个在S3有树突分支的神经节细胞强烈CR-IR。用地松鼠的抗CR或抗PV抗体,我们没有发现AII无长突细胞的证据。一个与兔子的DAP1-3细胞相似的无长突细胞是CR-IR和甘氨酸-IR。我们根据视网膜是以视杆还是视锥为主,讨论这种标记模式与其他哺乳动物物种的关系。所揭示的染色模式和表型差异表明,无长突细胞群体根据视网膜是以视杆还是视锥为主存在功能多样性。