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Role of Endosomes in Simian Virus 40 Entry and Infection▿†

机译:内体在猿猴病毒40进入和感染中的作用▿†

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摘要

After binding to its cell surface receptor ganglioside GM1, simian virus 40 (SV40) is endocytosed by lipid raft-mediated endocytosis and slowly transported to the endoplasmic reticulum, where partial uncoating occurs. We analyzed the intracellular pathway taken by the virus in HeLa and CV-1 cells by using a targeted small interfering RNA (siRNA) silencing screen, electron microscopy, and live-cell imaging as well as by testing a variety of cellular inhibitors and other perturbants. We found that the virus entered early endosomes, late endosomes, and probably endolysosomes before reaching the endoplasmic reticulum and that this pathway was part of the infectious route. The virus was especially sensitive to a variety of perturbations that inhibited endosome acidification and maturation. Contrary to our previous models, which postulated the passage of the virus through caveolin-rich organelles that we called caveosomes, we conclude that SV40 depends on the classical endocytic pathway for infectious entry.
机译:猿猴病毒40(SV40)与其细胞表面受体神经节苷脂GM1结合后,被脂质筏介导的内吞作用吞噬并缓慢转运到内质网,发生部分脱膜。我们通过使用靶向小干扰RNA(siRNA)沉默筛查,电子显微镜和活细胞成像,以及通过测试各种细胞抑制剂和其他干扰物,分析了病毒在HeLa和CV-1细胞中采取的细胞内途径。我们发现病毒在到达内质网之前进入了早期的内体,晚期的内体,甚至可能是内在的溶酶体,并且这种途径是感染途径的一部分。该病毒对抑制内体酸化和成熟的各种扰动特别敏感。与我们以前的模型相反,我们先前的模型假定病毒会通过称为小窝的富含小窝蛋白的细胞器传播,我们得出结论,SV40依赖于经典的内吞途径进行感染。

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