Pérez de Sevilla Müller Luis, Azar Shaghauyegh S, de Los Santos Janira, Brecha Nicholas C
Departments of Neurobiology, Medicine and Ophthalmology, David Geffen School of Medicine at Los Angeles, University of California, Los AngelesLos Angeles, CA, USA.
Stein Eye Institute, David Geffen School of Medicine at Los Angeles, University of California, Los AngelesLos Angeles, CA, USA.
Front Neuroanat. 2017 May 5;11:39. doi: 10.3389/fnana.2017.00039. eCollection 2017.
The transcription factor Prox1 is expressed in multiple cells in the retina during eye development. This study has focused on neuronal Prox1 expression in the inner nuclear layer (INL) of the adult mouse retina. Prox1 immunostaining was evaluated in vertical retinal sections and whole mount preparations using a specific antibody directed to the C-terminus of Prox1. Strong immunostaining was observed in numerous amacrine cell bodies and in all horizontal cell bodies in the proximal and distal INL, respectively. Some bipolar cells were also weakly immunostained. Prox1-immunoreactive amacrine cells expressed glycine, and they formed 35 ± 3% of all glycinergic amacrine cells. Intracellular Neurobiotin injections into AII amacrine cells showed that all gap junction-coupled AII amacrine cells express Prox1, and no other Prox1-immunostained amacrine cells were in the immediate area surrounding the injected AII amacrine cell. Prox1-immunoreactive amacrine cell bodies were distributed across the retina, with their highest density (3887 ± 160 cells/mm) in the central retina, 0.5 mm from the optic nerve head, and their lowest density (3133 ± 350 cells/mm) in the mid-peripheral retina, 2 mm from the optic nerve head. Prox1-immunoreactive amacrine cell bodies comprised ~9.8% of the total amacrine cell population, and they formed a non-random mosaic with a regularity index (RI) of 3.4, similar to AII amacrine cells in the retinas of other mammals. Together, these findings indicate that AII amacrine cells are the predominant and likely only amacrine cell type strongly expressing Prox1 in the adult mouse retina, and establish Prox1 as a marker of AII amacrine cells.
转录因子Prox1在眼睛发育过程中于视网膜的多种细胞中表达。本研究聚焦于成年小鼠视网膜内核层(INL)中神经元Prox1的表达。使用针对Prox1 C末端的特异性抗体,在垂直视网膜切片和整装标本中评估Prox1免疫染色。在近端和远端INL的众多无长突细胞体以及所有水平细胞体中分别观察到强免疫染色。一些双极细胞也有弱免疫染色。Prox1免疫反应性无长突细胞表达甘氨酸,它们占所有甘氨酸能无长突细胞的35±3%。向AII无长突细胞内注射细胞内神经生物素显示,所有缝隙连接耦合的AII无长突细胞均表达Prox1,并且在注射的AII无长突细胞周围的紧邻区域没有其他Prox1免疫染色的无长突细胞。Prox1免疫反应性无长突细胞体分布于整个视网膜,在距视神经乳头0.5 mm的中央视网膜中密度最高(3887±160个细胞/mm),在距视神经乳头2 mm的中周视网膜中密度最低(3133±350个细胞/mm)。Prox1免疫反应性无长突细胞体约占无长突细胞总数的9.8%,它们形成了规则指数(RI)为3.4的非随机镶嵌,类似于其他哺乳动物视网膜中的AII无长突细胞。总之,这些发现表明AII无长突细胞是成年小鼠视网膜中主要且可能唯一强烈表达Prox1的无长突细胞类型,并将Prox1确立为AII无长突细胞的标志物。