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大鼠肝窦内皮细胞中网格蛋白包被小窝的连续切片分析

Serial section analysis of clathrin-coated pits in rat liver sinusoidal endothelial cells.

作者信息

Goldenthal K L, Pastan I, Willingham M C

出版信息

Exp Cell Res. 1985 Dec;161(2):342-52. doi: 10.1016/0014-4827(85)90091-6.

DOI:10.1016/0014-4827(85)90091-6
PMID:2866104
Abstract

Electron microscopy and serial sections were used to examine the shape of clathrin-coated pits in sinusoidal endothelial cells of rat livers. Livers were perfused at 4 degrees C with either concanavalin A-horseradish peroxidase (conA-HRP), or HRP alone, followed by warm-up to 37 degrees C and fixation with glutaraldehyde. Alternatively, the livers were perfused with HRP at 37 degrees C, followed by fixation. All tissue was preserved using a membrane contrast enhancement technique (R-OTO) consisting of sequential osmium-ferrocyanide, thiocarbohydrazide, and osmium-ferrocyanide treatment. Peroxidase reaction product was used to identify structures participating in endocytosis. One hundred and ninety-three clathrin-coated structures were examined. Sixty-six were from livers perfused with conA-HRP at 4 degrees C, 63 were from livers perfused with only HRP at 4 degrees C, and 64 were from livers perfused with HRP at 37 degrees C. These coated structures were morphologically classified into three categories: (a) flat pits; (b) cup-shaped pits; (c) pits with a narrow neck. No isolated coated vesicles were found. In cells perfused at 4 degrees C followed by warming to 37 degrees C, the percentage of coated pits found connected to the cell surface by narrow necks was 31%, using conA-HRP, and 27% using HRP alone. In cells perfused continuously at 37 degrees C, the percentage of coated pits with narrow neck connections was 21% using HRP alone. These results suggest that the formation of coated pits connected to the surface by narrow necks is not an artifact of cell type, of experimental protocol or of incubation with a lectin.

摘要

采用电子显微镜和连续切片技术研究大鼠肝脏窦状内皮细胞中网格蛋白包被小窝的形态。肝脏在4℃下用伴刀豆球蛋白A - 辣根过氧化物酶(ConA - HRP)或仅用HRP灌注,然后升温至37℃并用戊二醛固定。或者,肝脏在37℃下用HRP灌注,随后固定。所有组织均采用一种膜对比度增强技术(R - OTO)保存,该技术包括依次进行锇 - 亚铁氰化物、硫代碳酰肼和锇 - 亚铁氰化物处理。过氧化物酶反应产物用于识别参与内吞作用的结构。共检查了193个网格蛋白包被结构。其中66个来自于在4℃下用ConA - HRP灌注的肝脏,63个来自于在4℃下仅用HRP灌注的肝脏,64个来自于在37℃下用HRP灌注的肝脏。这些包被结构在形态上分为三类:(a)扁平小窝;(b)杯状小窝;(c)颈部狭窄的小窝。未发现孤立的包被小泡。在4℃灌注后升温至37℃的细胞中,使用ConA - HRP时,通过狭窄颈部与细胞表面相连的包被小窝的百分比为31%,仅使用HRP时为27%。在37℃持续灌注的细胞中,仅使用HRP时,具有狭窄颈部连接的包被小窝的百分比为21%。这些结果表明,通过狭窄颈部与表面相连的包被小窝的形成不是细胞类型、实验方案或与凝集素孵育的人为产物。

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