Wässle H, Grünert U, Chun M H, Boycott B B
Max-Planck-Institut für Hirnforschung, Frankfurt, Federal Republic of Germany.
J Comp Neurol. 1995 Oct 23;361(3):537-51. doi: 10.1002/cne.903610315.
AII-amacrine cells were characterized from Golgi-stained sections and wholemounts of the macaque monkey retina. Similar to other mammalian retinae, they are narrow-field, bistratified amacrine cells with lobular appendages in the outer half of the inner plexiform layer (IPL) and a bushy, smoother dendritic tree in the inner half. AII cells of the monkey retina were stained immunocytochemically with antibodies against the calcium-binding protein calretinin. Their retinal mosaic was elaborated, and their density distribution across the retina was measured. Convergence within the rod pathway was calculated. Electron microscopy of calretinin-immunolabelled sections was used to study the synaptic connections of the AII cells. They receive a major input from rod bipolar cells, and their output is largely onto cone bipolar cells. Thus, the rod pathway of the primate retina follows the general mammalian scheme as it is known from the cat, the rabbit, and the rat retina. The spatial sampling properties of macaque AII-amacrine cells are discussed and related to human scotopic visual acuity.
从猕猴视网膜的高尔基染色切片和整装片中对AII无长突细胞进行了特征描述。与其他哺乳动物的视网膜相似,它们是窄视野、双分层的无长突细胞,在内网状层(IPL)外半部分有小叶状附属物,在内半部分有浓密、更平滑的树突分支。用抗钙结合蛋白钙视网膜蛋白的抗体对猕猴视网膜的AII细胞进行免疫细胞化学染色。阐述了它们的视网膜镶嵌,并测量了它们在整个视网膜上的密度分布。计算了视杆通路内的会聚情况。用钙视网膜蛋白免疫标记切片的电子显微镜研究AII细胞的突触连接。它们主要接受视杆双极细胞的输入,其输出主要作用于视锥双极细胞。因此,灵长类视网膜的视杆通路遵循从猫、兔和大鼠视网膜中已知的一般哺乳动物模式。讨论了猕猴AII无长突细胞的空间采样特性,并将其与人类暗视觉敏锐度相关联。