Willingham M C, Pastan I
Proc Natl Acad Sci U S A. 1983 Sep;80(18):5617-21. doi: 10.1073/pnas.80.18.5617.
The early events in the entry of ligands into cultured fibroblasts through plasma membrane clathrin-coated pits were examined by using serial sections and electron microscopy. Swiss 3T3 cells were labeled at 4 degrees C with concanavalin A-horseradish peroxidase and warmed to 37 degrees C for 1 or 2 min to label organelles participating in endocytosis. Cells were fixed in glutaraldehyde and further preserved with a membrane contrast-enhancement technique that utilized sequential osmium/ferrocyanide, thiocarbohydrazide, and osmium/ferrocyanide treatment in situ. This technique provides exceptional preservation and enhanced contrast of membranous structures. Serial sections taken both parallel to and perpendicular to the substratum were examined by electron microscopy, and 263 clathrin-coated structures containing horseradish peroxidase were evaluated for their connection to the plasma membrane. All of these coated structures were found to be connected to the plasma membrane either directly or via necks approximately equal to 170 A in width and up to 7,000 A in length. These necks were often surrounded by a dense filamentous network. These results strongly suggest that isolated coated vesicles do not form during the endocytosis process in Swiss 3T3 cells.
通过使用连续切片和电子显微镜,研究了配体通过质膜网格蛋白包被小窝进入培养成纤维细胞的早期事件。将瑞士3T3细胞在4℃下用伴刀豆球蛋白A - 辣根过氧化物酶标记,然后升温至37℃1或2分钟,以标记参与内吞作用的细胞器。细胞用戊二醛固定,并采用一种膜对比增强技术进一步保存,该技术利用原位依次进行锇/亚铁氰化物、硫代碳酰肼和锇/亚铁氰化物处理。该技术能提供出色的保存效果并增强膜结构的对比度。通过电子显微镜检查平行于和垂直于基质的连续切片,并对263个含有辣根过氧化物酶的网格蛋白包被结构与质膜的连接情况进行评估。发现所有这些包被结构都直接或通过宽度约为170埃、长度达7000埃的颈部与质膜相连。这些颈部常常被致密的丝状网络包围。这些结果强烈表明,在瑞士3T3细胞的内吞过程中不会形成孤立的包被小泡。