Singaravelu Ragunath, Srinivasan Prashanth, Pezacki John Paul
a Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
b Life Sciences Division, National Research Council Canada, Ottawa, ON K1A 0R6, Canada.
Can J Microbiol. 2015 Aug;61(8):521-30. doi: 10.1139/cjm-2015-0292. Epub 2015 Jun 10.
The metabolic interplay between hosts and viruses plays a crucial role in determining the outcome of viral infection. Viruses reorchestrate the host's primary metabolic gene networks, including genes associated with mevalonate and isoprenoid synthesis, to acquire the necessary energy and structural components for their viral life cycles. Recent work has demonstrated that the interferon-mediated antiviral response suppresses the sterol pathway through production of a signalling molecule, 25-hydroxycholesterol (25HC). This oxysterol has been shown to exert multiple effects, both through incorporation into host cellular membranes as well as through transcriptional control. Herein, we summarize our current understanding of the multifunctional roles of 25HC in the mammalian innate antiviral response.
宿主与病毒之间的代谢相互作用在决定病毒感染的结果中起着关键作用。病毒重新编排宿主的主要代谢基因网络,包括与甲羟戊酸和类异戊二烯合成相关的基因,以获取其病毒生命周期所需的能量和结构成分。最近的研究表明,干扰素介导的抗病毒反应通过产生一种信号分子25-羟基胆固醇(25HC)来抑制甾醇途径。这种氧化甾醇已被证明具有多种作用,既可以通过掺入宿主细胞膜,也可以通过转录控制来实现。在此,我们总结了目前对25HC在哺乳动物先天性抗病毒反应中的多功能作用的理解。