Steer Sarah A, Corbett John A
Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, Missouri 63104, USA.
Viral Immunol. 2003;16(4):447-60. doi: 10.1089/088282403771926283.
Prostaglandins are lipid mediators, generated by cyclooxygenase (COX), that have been shown to participate in the regulation of virus replication and the modulation of inflammatory responses following infection. A number of studies support a role for PGE2 in the modulation of virus replication and virulence in a cell type and virus selective manner. Virus infection also stimulates the expression of a number of proinflammatory gene products, including COX-2, inducible nitric oxide synthase (iNOS) as well as proinflammatory cytokines. This review will focus on the mechanisms by which proinflammatory prostaglandin production regulates virus replication and virulence. In addition, the signaling pathways that are activated during a virus infection, and that regulate proinflammatory gene expression in macrophages will be reviewed. Specific attention will be placed on the ability of virus infection to activate multiple signaling cascades (such as PKR, MAPK, iPLA2, NF-kappaB) and how these pathways are integrated in the regulation of individual target gene expression.
前列腺素是由环氧化酶(COX)产生的脂质介质,已被证明参与病毒复制的调节以及感染后炎症反应的调节。许多研究支持前列腺素E2(PGE2)在以细胞类型和病毒选择性方式调节病毒复制和毒力方面的作用。病毒感染还会刺激多种促炎基因产物的表达,包括COX-2、诱导型一氧化氮合酶(iNOS)以及促炎细胞因子。本综述将聚焦于促炎性前列腺素产生调节病毒复制和毒力的机制。此外,还将综述病毒感染期间激活的、调节巨噬细胞中促炎基因表达的信号通路。将特别关注病毒感染激活多个信号级联反应(如蛋白激酶R(PKR)、丝裂原活化蛋白激酶(MAPK)、钙依赖性磷脂酶A2(iPLA2)、核因子κB(NF-κB))的能力,以及这些通路如何整合到单个靶基因表达的调节中。