Suppr超能文献

大鼠睾丸网衬里上皮细胞中的内吞作用。

Endocytosis in epithelial cells lining the rete testis of the rat.

作者信息

Morales C, Hermo L, Clermont Y

出版信息

Anat Rec. 1984 Jun;209(2):185-95. doi: 10.1002/ar.1092090206.

Abstract

The endocytic activity of the low cuboidal cells lining the rete testis was analyzed by electron microscopy following injection of various tracers into the lumen of these anastomotic channels. At 1 and 5 minutes after injection, cationic ferritin (CF) and concanavalin A-ferritin (Con A) were seen bound to the apical plasma membrane and to the membrane of subjacent vesicles or invaginations connected to this apical membrane. At 30 and 60 minutes, these tracers were found in intracytoplasmic vesicles and in vesicles connected to the lateral or basal plasma membrane as well as in the lateral intercellular space and in the lamina lucida of basal lamina. At 30 minutes, CF and Con A also appeared in the matrix of pale multivesicular bodies while at 1 hour dense multivesicular bodies were labeled. At 2 hours and later time intervals, the tracers accumulated in dense granules identified as lysosomes. Native ferritin (NF), concanavalin A-ferritin in presence of alpha-methyl-D-mannoside, and horseradish peroxidase or albumin bound to colloidal gold were all to be incorporated by the lysosomal system of these epithelial cells, as just described for CF and Con A, but these various tracers were not bound to the apical plasma membrane or to the membrane of cytoplasmic vesicles, nor were they found in the intercellular spaces or the lamina lucida at the base of the cells. Thus, the epithelial cells of the rete testis do not appear to be only involved in the uptake of substances from the lumen and their disposal by the lysosomal system, but also appear to contribute to the transport of certain macromolecules from the lumen to the laterobasal surfaces of the cells. These cells may thus play a role in determining the composition of the rete testis fluid.

摘要

在将各种示踪剂注入这些吻合通道的管腔后,通过电子显微镜分析了睾丸网内衬低立方体细胞的内吞活性。注射后1分钟和5分钟,可见阳离子铁蛋白(CF)和伴刀豆球蛋白A-铁蛋白(Con A)结合在顶端质膜以及与该顶端膜相连的下方囊泡或内陷的膜上。在30分钟和60分钟时,这些示踪剂出现在细胞质囊泡中以及与外侧或基底质膜相连的囊泡中,也出现在细胞间外侧间隙和基底膜的透明层中。在30分钟时,CF和Con A也出现在淡色多囊泡体的基质中,而在1小时时,深色多囊泡体被标记。在2小时及以后的时间间隔,示踪剂积聚在被鉴定为溶酶体的致密颗粒中。天然铁蛋白(NF)、存在α-甲基-D-甘露糖苷时的伴刀豆球蛋白A-铁蛋白以及与胶体金结合的辣根过氧化物酶或白蛋白都将被这些上皮细胞的溶酶体系统摄取,正如刚才对CF和Con A所描述的那样,但这些不同的示踪剂没有结合到顶端质膜或细胞质囊泡的膜上,也没有在细胞间间隙或细胞底部的透明层中发现。因此,睾丸网的上皮细胞似乎不仅参与从管腔摄取物质并通过溶酶体系统进行处理,而且似乎还参与将某些大分子从管腔运输到细胞的外侧基底表面。因此,这些细胞可能在确定睾丸网液的成分中起作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验