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大鼠输出小管非纤毛上皮细胞中的内吞作用。

Endocytosis in nonciliated epithelial cells of the ductuli efferentes in the rat.

作者信息

Hermo L, Morales C

出版信息

Am J Anat. 1984 Sep;171(1):59-74. doi: 10.1002/aja.1001710106.

Abstract

The nonciliated cells lining the ductuli efferentes presented three distinct cytoplasmic regions. The apical region contained, in addition to cisternae of endoplasmic reticulum and mitochondria, two distinct membranous elements. The tubulovesicular system consisted of dilated tubules connected to the apical plasma membrane and subjacent distended vesicular profiles. The apical tubules, not connected to the cell surface, consisted of numerous densely stained tubules of small size which contain a compact, finely granulated material. The supranuclear region, in addition to a Golgi apparatus and ER cisternae, contained dilated vacuoles, pale and dense multivesicular bodies, as well as numerous dense granules identified cytochemically as lysosomes. The basal region contained the nucleus and many lipid droplets. The endocytic activity of these cells was investigated using cationic ferritin (CF) and concanavalin-A-ferritin (Con-A-ferritin) as markers of adsorptive endocytosis; and native ferritin (NF), concanavalin-A-ferritin in the presence of alpha-methyl mannoside, and horseradish peroxidase or albumin bound to colloidal gold for demonstrating fluid-phase endocytosis. These tracers were injected separately into the rete testis, and animals were sacrificed at various time intervals after injection. At 1 min, CF or Con-A-ferritin were seen bound to the apical plasma membrane, to the membrane of microvilli, and to the membrane delimiting elements of the tubulovesicular system. Between 2 and 5 min, these tracers accumulated in the densely stained apical tubules and at 15 min in the dilated vacuoles. Between 30 min and 1 hr, the tracers appeared in multivesicular bodies of progressively increasing density, whereas at 2 hr and later time intervals, many dense lysosomal elements became labeled. The tracers for fluid-phase endocytosis showed a distribution similar to that for CF or Con-A-ferritin except that they did not bind to the apical plasma membrane, microvilli, or membrane delimiting the tubulovesicular system. At no time interval were any of the tracers observed in the abluminal spaces. Thus, the nonciliated epithelial cells of the ductuli efferentes are actively involved in fluid-phase and adsorptive endocytosis, both of which result in the sequestration of endocytosed material within the lysosomal apparatus of the cell.

摘要

输出小管内衬的无纤毛细胞呈现出三个不同的细胞质区域。顶端区域除了含有内质网池和线粒体之外,还有两种不同的膜性成分。微管泡系统由与顶端质膜相连的扩张小管以及其下方扩张的泡状结构组成。顶端小管不与细胞表面相连,由许多小的、深染的小管组成,这些小管含有致密的、细颗粒状物质。核上区域除了有高尔基体和内质网池之外,还含有扩张的液泡、浅色和深色的多泡体,以及通过细胞化学鉴定为溶酶体的许多致密颗粒。基部区域含有细胞核和许多脂滴。使用阳离子铁蛋白(CF)和伴刀豆球蛋白A-铁蛋白(Con-A-铁蛋白)作为吸附性内吞作用的标志物,以及天然铁蛋白(NF)、存在α-甲基甘露糖苷时的伴刀豆球蛋白A-铁蛋白,和与胶体金结合的辣根过氧化物酶或白蛋白来研究这些细胞的内吞活性,以证明液相内吞作用。将这些示踪剂分别注入睾丸网,在注射后的不同时间间隔处死动物。在1分钟时,可见CF或Con-A-铁蛋白与顶端质膜、微绒毛膜以及微管泡系统的膜界定成分结合。在2至5分钟之间,这些示踪剂积聚在深染的顶端小管中,在15分钟时积聚在扩张的液泡中。在30分钟至1小时之间,示踪剂出现在密度逐渐增加的多泡体中,而在2小时及以后的时间间隔,许多致密的溶酶体成分被标记。液相内吞作用的示踪剂显示出与CF或Con-A-铁蛋白相似的分布,只是它们不与顶端质膜、微绒毛或界定微管泡系统的膜结合。在任何时间间隔都未在管腔外间隙观察到任何示踪剂。因此,输出小管的无纤毛上皮细胞积极参与液相和吸附性内吞作用,这两种作用都会导致内吞物质在细胞的溶酶体装置中被隔离。

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