Bokoch Gary M, Zhao Tieming
Department of Immunology, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037, USA.
Antioxid Redox Signal. 2006 Sep-Oct;8(9-10):1533-48. doi: 10.1089/ars.2006.8.1533.
Phagocytic leukocytes generate reactive oxygen species important for the killing of invading microorganisms. The source of these oxidants is the NADPH oxidase, a tightly controlled multicomponent enzyme made up of a membrane-associated catalytic moiety and cytosolic regulatory components that must assemble to form the active oxidase. The phagocyte NADPH oxidase was the first mammalian system shown to be directly regulated by a Rac GTPase. We review here our understanding of NADPH oxidase regulation by Rac, as well as the regulation of Rac itself, in phagocytic leukocytes. Rather than viewing Rac as a "cog" in the NADPH oxidase machinery, we argue for a view of Rac GTPases as critical "molecular switches" regulating the formation of ROS by phagocytic leukocytes under physiologic and pathologic conditions.
吞噬性白细胞产生对杀灭入侵微生物很重要的活性氧。这些氧化剂的来源是NADPH氧化酶,它是一种受到严格调控的多组分酶,由一个膜相关催化部分和胞质调节成分组成,这些成分必须组装形成活性氧化酶。吞噬细胞NADPH氧化酶是第一个被证明受Rac GTP酶直接调控的哺乳动物系统。我们在此综述我们对吞噬性白细胞中Rac对NADPH氧化酶的调控以及Rac自身调控的理解。我们认为不应将Rac视为NADPH氧化酶机制中的一个“齿轮”,而应将Rac GTP酶视为在生理和病理条件下调节吞噬性白细胞ROS形成的关键“分子开关”。