Suppr超能文献

猴病毒40对主要组织相容性复合体I类分子和小窝的利用

Exploitation of major histocompatibility complex class I molecules and caveolae by simian virus 40.

作者信息

Parton R G, Lindsay M

机构信息

Department of Physiology and Pharmacology, University of Queensland, Brisbane, Australia.

出版信息

Immunol Rev. 1999 Apr;168:23-31. doi: 10.1111/j.1600-065x.1999.tb01280.x.

Abstract

Simian virus 40 (SV40), a non-enveloped DNA virus, is transported from the cell surface to the nucleus where virus replication occurs. This pathway of virus uptake involves binding to surface MHC class I molecules, entry via non-coated pits, and subsequent transport to the endoplasmic reticulum (ER). At some stage in this pathway the virus must cross a membrane to reach the cytosol. In the present review, the cellular machinery which the virus has utilized to enter the cell will be examined. In particular, we will consider recent evidence for the involvement of caveolae in the infectious entry step and propose a model involving recruitment of caveolar proteins around the membrane-bound virus. We also speculate that a similar mechanism may have been exploited by bacterial pathogens. The subsequent steps by which SV40 reaches the ER remain unclear but recent evidence suggests that this pathway may be shared with several other proteins that are transported from surface caveolae to the ER.

摘要

猴病毒40(SV40)是一种无包膜的DNA病毒,它从细胞表面转运至病毒进行复制的细胞核。这种病毒摄取途径包括与表面MHC I类分子结合、通过无被小窝进入,随后转运至内质网(ER)。在该途径的某个阶段,病毒必须穿过一层膜才能到达细胞质溶胶。在本综述中,将研究病毒用于进入细胞的细胞机制。特别是,我们将考虑小窝在感染性进入步骤中发挥作用的最新证据,并提出一个涉及在膜结合病毒周围募集小窝蛋白的模型。我们还推测细菌病原体可能利用了类似的机制。SV40随后到达内质网的步骤仍不清楚,但最近的证据表明,这条途径可能与其他几种从表面小窝转运至内质网的蛋白质所共有的。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验