Goldenthal K L, Pastan I, Willingham M C
Exp Cell Res. 1984 Jun;152(2):558-64. doi: 10.1016/0014-4827(84)90658-x.
We have examined the shape and distribution of clathrin-coated pits in Swiss 3T3 cells at 4 or 37 degrees C using electron microscopy with serial sections and immunofluorescence light microscopy. Both groups were fixed in glutaraldehyde and preserved further using a membrane contrast enhancement technique consisting of sequential osmium-ferrocyanide, thiocarbohydrazide and osmium-ferrocyanide treatment in situ. Concanavalin A-horseradish peroxidase (conA-HRP) was used to identify these structures participating in endocytosis. Two hundred twenty-two clathrin-coated structures were analysed; 126 from cells fixed at 4 degrees C, and 96 from cells fixed after a 3 min warm-up to 37 degrees C. All coated structures labeled with conA-HRP had demonstrable connections to the plasma membrane. These coated structures were morphologically classified into three categories: (a) flat pits; (b) curved pits; and (c) pits with narrow-neck connections to the plasma membrane. At 37 degrees C, 27% of coated pits had narrow neck connections to the plasma membrane whereas at 4 degrees C only 1% had such connections. Receptosomes (endosomes) labeled with conA-HRP were found only after incubation at 37 degrees C, indicating that active endocytosis was occurring in cells at 37 degrees C, but not at 4 degrees C. Immunofluorescence with anti-clathrin antibody was used to quantitate the number of clathrin-coated pits in Swiss 3T3 cells incubated at 4 and 37 degrees C prior to fixation. No difference was detected. There were 426 +/- 122 pits per cell at 37 degrees C and 441 +/- 106 at 4 degrees C. These results support the hypothesis that formation of a narrow neck connected a coated pit to the cell surface is an early step in the mechanism of receptor-mediated endocytosis.
我们运用连续切片电子显微镜和免疫荧光光学显微镜,研究了处于4℃或37℃的瑞士3T3细胞中网格蛋白包被小窝的形态和分布。两组细胞均用戊二醛固定,并采用一种膜反差增强技术进一步保存,该技术包括原位依次进行锇-亚铁氰化物、硫代碳酰肼和锇-亚铁氰化物处理。伴刀豆球蛋白A-辣根过氧化物酶(ConA-HRP)用于识别参与内吞作用的这些结构。分析了222个网格蛋白包被结构;其中126个来自于4℃固定的细胞,96个来自于升温至37℃保温3分钟后固定的细胞。所有用ConA-HRP标记的包被结构都与质膜有明显连接。这些包被结构在形态上分为三类:(a)扁平小窝;(b)弯曲小窝;(c)与质膜有窄颈连接的小窝。在37℃时,27%的包被小窝与质膜有窄颈连接,而在4℃时只有1%有此类连接。仅在37℃孵育后才发现用ConA-HRP标记的受体小体(内体),这表明37℃的细胞中发生了活跃的内吞作用,而4℃时则没有。在固定前用抗网格蛋白抗体进行免疫荧光,以定量分析处于4℃和37℃孵育的瑞士3T3细胞中网格蛋白包被小窝的数量。未检测到差异。37℃时每个细胞有426±122个小窝,4℃时为441±106个。这些结果支持了这样的假说,即形成连接包被小窝与细胞表面的窄颈是受体介导的内吞作用机制中的早期步骤。