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大鼠膀胱移行上皮表层细胞中不对称单位膜的周转

Turnover of asymmetric unit membranes in the transitional epithelial superficial cells of the rat urinary bladder.

作者信息

Amano O, Kataoka S, Yamamoto T Y

机构信息

Department of Anatomy, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Anat Rec. 1991 Jan;229(1):9-15. doi: 10.1002/ar.1092290103.

Abstract

Asymmetric thick unit membranes were observed on the luminal surface, fusiform vesicles, and multivesicular bodies of superficial cells of rat transitional epithelium. When HRP-labeled Ricinus communis lectin (RCA-I) was injected into the rat urinary bladder, RCA-I was deposited along the luminal cell membrane and in some multivesicular bodies, but not in the fusiform vesicles either before or after contraction. When the bladder was sliced by Vibratome and stained with HRP-labeled RCA-I after fixation, RCA-I was observed in many cell organelles, including fusiform vesicles and multivesicular bodies as well as the luminal surface. When small pieces of tissue were stained en-bloc with HRP-labeled RCA-I, RCA-I was found along the luminal cell surface but not in the fusiform vesicles nor the multivesicular bodies. When HRP alone was injected into the bladder, HRP was observed in some multivesicular bodies after contraction but not in the fusiform vesicles. Various lysosomes were observed by electron microscopy. Some were wrapping multivesicular bodies in ringlike fashion, and some contained asymmetric unit membranes. These findings suggest that the asymmetric unit membranes are carried to the luminal cell membrane via the fusiform vesicles and that old luminal cell membranes are removed via the multivesicular bodies to be degraded by lysosomes.

摘要

在大鼠移行上皮表层细胞的管腔表面、梭形小泡和多泡体上观察到不对称的厚单位膜。当将辣根过氧化物酶标记的蓖麻凝集素(RCA-I)注入大鼠膀胱时,RCA-I沉积在管腔细胞膜和一些多泡体上,但在收缩前后的梭形小泡中均未发现。当用振动切片机将膀胱切片并在固定后用辣根过氧化物酶标记的RCA-I染色时,在许多细胞器中观察到RCA-I,包括梭形小泡、多泡体以及管腔表面。当用辣根过氧化物酶标记的RCA-I对小块组织进行整体染色时,在管腔细胞表面发现了RCA-I,但在梭形小泡和多泡体中未发现。当单独将辣根过氧化物酶注入膀胱时,收缩后在一些多泡体中观察到辣根过氧化物酶,但在梭形小泡中未观察到。通过电子显微镜观察到各种溶酶体。一些以环状方式包裹多泡体,一些含有不对称单位膜。这些发现表明,不对称单位膜通过梭形小泡被运输到管腔细胞膜,而旧的管腔细胞膜通过多泡体被清除,由溶酶体进行降解。

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