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病毒对细胞周期的操纵。

Virus manipulation of cell cycle.

机构信息

Instituto Gulbenkian de Ciencia, Oeiras, Portugal.

出版信息

Protoplasma. 2012 Jul;249(3):519-28. doi: 10.1007/s00709-011-0327-9. Epub 2011 Oct 11.

DOI:10.1007/s00709-011-0327-9
PMID:21986922
Abstract

Viruses depend on host cell resources for replication and access to those resources may be limited to a particular phase of the cell cycle. Thus manipulation of cell cycle is a commonly employed strategy of viruses for achieving a favorable cellular environment. For example, viruses capable of infecting nondividing cells induce S phase in order to activate the host DNA replication machinery and provide the nucleotide triphosphates necessary for viral DNA replication (Flemington in J Virol 75:4475-4481, 2001; Sullivan and Pipas in Microbiol Mol Biol Rev 66:179-202, 2002). Viruses have developed several strategies to subvert the cell cycle by association with cyclin and cyclin-dependent kinase complexes and molecules that regulate their activity. Viruses tend to act on cellular proteins involved in a network of interactions in a way that minimal protein-protein interactions lead to a major effect. The complex and interactive nature of intracellular signaling pathways controlling cell division affords many opportunities for virus manipulation strategies. Taking the maxim "Set a thief to catch a thief" as a counter strategy, however, provides us with the very same virus evasion strategies as "ready-made tools" for the development of novel antivirus therapeutics. The most obvious are attenuated virus vaccines with critical evasion genes deleted. Similarly, vaccines against viruses causing cancer are now being successfully developed. Finally, as viruses have been playing chess with our cell biology and immune responses for millions of years, the study of their evasion strategies will also undoubtedly reveal new control mechanisms and their corresponding cellular intracellular signaling pathways.

摘要

病毒依赖宿主细胞的资源进行复制,而这些资源的获取可能仅限于细胞周期的特定阶段。因此,操纵细胞周期是病毒实现有利细胞环境的常用策略。例如,能够感染非分裂细胞的病毒会诱导 S 期,以激活宿主 DNA 复制机制,并提供病毒 DNA 复制所需的核苷酸三磷酸(Flemington,J Virol 75:4475-4481,2001;Sullivan 和 Pipas,Microbiol Mol Biol Rev 66:179-202,2002)。病毒通过与细胞周期蛋白和细胞周期蛋白依赖性激酶复合物以及调节其活性的分子结合,发展了几种破坏细胞周期的策略。病毒倾向于作用于参与细胞相互作用网络的细胞蛋白,从而以最小的蛋白-蛋白相互作用产生主要影响。控制细胞分裂的细胞内信号通路的复杂和交互性质为病毒操纵策略提供了许多机会。然而,采用“以毒攻毒”的策略,为我们提供了与病毒逃避策略相同的现成工具,用于开发新的抗病毒治疗方法。最明显的是删除关键逃避基因的减毒病毒疫苗。同样,针对导致癌症的病毒的疫苗现在也正在成功开发中。最后,由于病毒与我们的细胞生物学和免疫反应已经博弈了数百万年,因此研究它们的逃避策略无疑也将揭示新的控制机制及其相应的细胞内信号通路。

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