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AtT20细胞中被阻断的有被小窝是由出芽逆转录病毒的内吞作用导致的。

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

作者信息

Tooze J

出版信息

J Cell Biol. 1985 Nov;101(5 Pt 1):1713-23. doi: 10.1083/jcb.101.5.1713.

Abstract

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.

摘要

AtT20细胞支持两种内源性逆转录病毒的复制,一种是鼠白血病病毒,另一种是小鼠乳腺肿瘤病毒。在玻璃或塑料基质上,AtT20细胞成簇生长。在这种情况下,从一个细胞的质膜上出芽的逆转录病毒,在极少数情况下,会被相邻细胞的质膜上的包被小窝摄取。这些小窝可以向内凹陷到细胞质中2000 - 4000埃的深度,同时将病毒芽体一起吸入,这些芽体通过管状柄与它们的亲代细胞相连,其中一些管状柄的直径只有225±15埃。这些柄从芽体沿着小窝的直管延伸到亲代细胞表面。几条证据表明,这些独特的结构被阻断,使得内吞作用和出芽都无法完成,并且它们会持续几个小时。这些被阻断的包被小窝的特性与内吞作用和病毒出芽的模型都相关。首先,它们表明包被小窝的内陷并不绝对依赖于其掐断形成包被囊泡,但脱包被似乎依赖于游离囊泡的产生。其次,它们表明逆转录病毒核心成熟为成熟核样体的最后阶段依赖于芽体与其亲代细胞的分离,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,但还是对这些结构的形成给出了一种解释。

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1
Adsorptive endocytosis of Semliki Forest virus.辛德毕斯病毒的吸附性内吞作用。
J Mol Biol. 1980 Sep 25;142(3):439-54. doi: 10.1016/0022-2836(80)90281-8.
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Entry of murine retrovirus into mouse fibroblasts.鼠逆转录病毒进入小鼠成纤维细胞。
Virology. 1983 Feb;125(1):85-98. doi: 10.1016/0042-6822(83)90065-x.
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