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细胞骨架框架与脊髓灰质炎病毒代谢

The cytoskeletal framework and poliovirus metabolism.

作者信息

Lenk R, Penman S

出版信息

Cell. 1979 Feb;16(2):289 301. doi: 10.1016/0092-8674(79)90006-0.

Abstract

The cytoskeletal framework prepared by detergent lysis of suspension-grown HeLa cells is compared to the structure obtained from poliovirus-infected cells. This framework, which retains major features of cell morphology and carries the cellular polyribosomes as well as the major structural filaments, is profoundly reorganized following virus infection. This reorganization underlies, at least in part, the morphological changes termed the "cytoplasmic effect." These cytoskeletal changes appear related to the involvement of the framework with viral-specific metabolism. Extensive cytoskeleton alterations occur even when guanidine inhibits viral replication, and thus result from small amounts of early viral products. The normally spheroidal nucleus deforms, allowing a modified region of the cytoplasm to occupy a central position in the cell, and many membrane-enclosed vesicles peculiar to the infected cell are elaborated here. The skeleton preparation reveals that this region contains intermediate filaments arranged in a pattern unique to infected cells. Further changes occur when viral replication is permitted. The central region filaments become coated with darkly staining material which may be viral RNA. Numerous small particles appear on the filaments which resemble partially assembled virions. Mature virions, however, have no affinity for the cytoskeleton and appear to be free in the cytoplasm. Host cell messenger RNA, normally attached to the skeletal framework, is released in infected cells and is replaced by the viral-specific polyribosomes. The trabecular network which carries polyribosomes appears to be rearranged; the viral polyribosomes are located principally at the cell periphery and are excluded from the central region. The viral replication complex with its double-stranded RNA is also attached to the skeletal framework and may comprise the dark staining material coating the filaments of the central cell region.

摘要

将悬浮培养的HeLa细胞经去污剂裂解制备的细胞骨架框架与脊髓灰质炎病毒感染细胞所获得的结构进行比较。该框架保留了细胞形态的主要特征,并携带细胞多核糖体以及主要的结构细丝,在病毒感染后会发生深刻的重组。这种重组至少部分地构成了被称为“细胞质效应”的形态变化的基础。这些细胞骨架变化似乎与该框架参与病毒特异性代谢有关。即使胍抑制病毒复制,广泛的细胞骨架改变仍会发生,因此是由少量早期病毒产物导致的。正常呈球形的细胞核变形,使细胞质的一个修饰区域占据细胞中心位置,并且在此处形成许多感染细胞特有的膜包裹小泡。骨架制备显示该区域含有以感染细胞特有的模式排列的中间丝。当允许病毒复制时会发生进一步的变化。中央区域的细丝被可能是病毒RNA的深色染色物质覆盖。细丝上出现许多类似于部分组装的病毒粒子的小颗粒。然而,成熟的病毒粒子对细胞骨架没有亲和力,似乎在细胞质中是游离的。通常附着在骨架框架上的宿主细胞信使RNA在感染细胞中被释放,并被病毒特异性多核糖体取代。携带多核糖体的小梁网络似乎被重新排列;病毒多核糖体主要位于细胞周边,被排除在中央区域之外。带有双链RNA的病毒复制复合体也附着在骨架框架上,可能构成覆盖细胞中央区域细丝的深色染色物质。

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