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通过HVJ(仙台病毒)使麦迪逊-达比犬肾细胞融合:病毒颗粒与膜融合位点无直接关联。

Fusion of Madin-Darby canine kidney cells by HVJ (Sendai virus): absence of direct association of virus particles with the site of membrane fusion.

作者信息

Kim J, Adachi T, Yoneda Y, Okada Y

机构信息

Institute of Molecular and Cellular Biology for Pharmaceutical Sciences, Kyoto Pharmaceutical University, Japan.

出版信息

Eur J Cell Biol. 1990 Feb;51(1):128-34.

PMID:2158447
Abstract

The process of cell fusion of Madin-Darby canine kidney (MDCK) cells by HVJ (Sendai virus) was investigated to determine whether the HVJ particles were directly associated with the site of membrane fusion. Confluent monolayer cultures of MDCK cells are sealed together by tight junctions on the apices of their lateral membranes, so added virus particles can be adsorbed only to the apical surfaces of the cells. After incubation with HVJ at 37 degrees C for 30 min, the cells still appeared mononucleate and unfused by light microscopy, but electron microscopic examination showed that fusion at the lateral membranes had occurred below the tight junctions. Furthermore, when fluorescein isothiocyanate (FITC)-labeled macromolecules, which cannot pass across the gap junctions, were injected into the cells at this stage, labeled macromolecules were found to diffuse into the adjacent cells. These findings strongly suggest that cell fusion was initiated in the lateral membrane, a region distinct from the site of adsorbed HVJ particles. Thus, the virus particles were not directly associated with the fusion site, but induced fusion of the lateral membranes indirectly.

摘要

研究了仙台病毒(HVJ)介导的犬肾传代细胞(MDCK)的细胞融合过程,以确定HVJ颗粒是否直接与膜融合位点相关联。MDCK细胞的汇合单层培养物通过其侧膜顶端的紧密连接密封在一起,因此添加的病毒颗粒只能吸附到细胞的顶端表面。在37℃下用HVJ孵育30分钟后,光镜下细胞仍呈单核且未融合,但电镜检查显示侧膜在紧密连接下方发生了融合。此外,在此阶段将不能穿过间隙连接的异硫氰酸荧光素(FITC)标记的大分子注入细胞时,发现标记的大分子扩散到相邻细胞中。这些发现强烈表明细胞融合起始于侧膜,该区域与吸附的HVJ颗粒位点不同。因此,病毒颗粒不直接与融合位点相关联,而是间接诱导侧膜融合。

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