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Blocked coated pits in AtT20 cells result from endocytosis of budding retrovirions

机译:AtT20细胞中包被的凹坑被堵塞是由于萌芽的逆转录病毒颗粒的内吞作用

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摘要

AtT20 cells support the replication of two endogenous retroviruses, a murine leukemia virus and a mouse mammary tumor virus. On glass or plastic substrates, AtT20 cells grow in clumps. In this situation, retroviruses budding from the plasma membrane of one cell can, on rare occasions, be invested by coated pits in the plasma membranes of contiguous cells. These pits can invaginate to depths of 2,000-4,000 A within the cytoplasm drawing with them the viral buds which remain connected to their parental cells by tubular stalks, some of which are only 225 +/- 15 A in diameter. These stalks run down the straight necks of the pits from the buds to the parental cell surfaces. Several lines of evidence indicate that these unique structures are blocked such that neither endocytosis nor budding can go to completion, and that they persist for several hours. The properties of these blocked coated pits are relevant to models of both endocytosis and viral budding. First, they indicate that the invagination of a coated pit is not absolutely dependent on its pinching off to form a coated vesicle, but that uncoating appears to be dependent upon the generation of a free vesicle. Secondly, they suggest that the final stages in the maturation of a retroviral core into a mature nucleoid are dependent on the detachment of the bud from its parental cell and that the driving force of budding is the association of viral transmembrane proteins with viral core proteins. An explanation is offered to account for the formation of these structures despite the phenomenon of viral interference.
机译:AtT20细胞支持两种内源性逆转录病毒的复制,一种鼠白血病病毒和一种小鼠乳腺肿瘤病毒。在玻璃或塑料基板上,AtT20细胞成团生长。在这种情况下,从一个细胞的质膜萌芽的逆转录病毒在极少数情况下可以通过连续细胞质膜上的包膜凹坑进行投资。这些凹坑可在细胞质内侵入到2000-4000 A的深度,从而使病毒芽通过管状茎杆保持与其亲代细胞的连接,其中一些茎直径仅为225 +/- 15A。这些茎沿着芽的直颈向下延伸,从芽到亲代细胞表面。几条证据表明,这些独特的结构被封闭,因此内吞作用和出芽都无法完全完成,并且持续了几个小时。这些封闭的包膜凹坑的性质与胞吞作用和病毒出芽的模型有关。首先,它们表明包被的凹坑的内陷并不完全取决于其捏捏形成包被的囊泡,但是未包被似乎取决于自由囊泡的产生。其次,他们认为逆转录病毒核心成熟为成熟核糖体的最后阶段取决于芽从其亲代细胞的脱离,并且出芽的驱动力是病毒跨膜蛋白与病毒核心蛋白的结合。尽管存在病毒干扰现象,但仍提供了解释说明这些结构的形成。

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