Mills S L, Massey S C
Sensory Sciences Center, Graduate School of Biomedical Sciences, University of Texas Health Science Center, Houston 77030.
J Comp Neurol. 1991 Feb 15;304(3):491-501. doi: 10.1002/cne.903040312.
The fluorescent dye 4,6-diamino-2-phenylindole (DAPI) has previously been used to label starburst amacrine cells selectively in the rabbit retina and AII amacrine cells in the cat retina. Using the rabbit retina, we show that intraocular injection of DAPI labels starburst amacrine cells as seen 1-2 days later. In contrast, after a brief in vitro incubation with DAPI, AII amacrine cells are selectively labeled. Amacrine cells were identified by intracellular staining with Lucifer Yellow. AII amacrine cells are arranged in a regular mosaic with a density of 2,800 cells/mm2 near the visual streak declining to about 500 cells/mm2 in the far periphery. The coverage of the lobular dendritic field in sublamina alpha is approximately 1.5 across the retina, but the coverage of the fine dendritic field in sublamina b increases from 3 centrally to 4 in the inferior periphery, and to above 8 in the superior periphery.
荧光染料4,6-二氨基-2-苯基吲哚(DAPI)此前已被用于选择性标记兔视网膜中的星爆无长突细胞和猫视网膜中的AII无长突细胞。利用兔视网膜,我们发现眼内注射DAPI后,1至2天可见星爆无长突细胞被标记。相比之下,在与DAPI进行短暂体外孵育后,AII无长突细胞被选择性标记。通过用路西法黄进行细胞内染色来识别无长突细胞。AII无长突细胞呈规则镶嵌排列,在视条纹附近密度为2800个细胞/mm²,在外周远侧降至约500个细胞/mm²。在视网膜中,α亚层小叶状树突野的覆盖范围约为1.5,但b亚层精细树突野的覆盖范围从中央的3增加到下外周的4,再到上外周的8以上。