Healy Laura D, Rigg Rachel A, Griffin John H, McCarty Owen J T
Department of Molecular Medicine, The Scripps Research Institute, La Jolla, California, USA.
Department of Cell, Developmental and Cancer Biology, Oregon Health and Science University, Portland, Oregon, USA.
J Leukoc Biol. 2018 Mar 30. doi: 10.1002/JLB.3MIR0817-338R.
Innate immune cells are an essential part of the host defense response, promoting inflammation through release of proinflammatory cytokines or formation of neutrophil extracellular traps. While these processes are important for defense against infectious agents or injury, aberrant activation potentiates pathologic inflammatory disease. Thus, understanding regulatory mechanisms that limit neutrophil extracellular traps formation and cytokine release is of therapeutic interest for targeting pathologic diseases. Activated protein C is an endogenous serine protease with anticoagulant activity as well as anti-inflammatory and cytoprotective functions, the latter of which are mediated through binding cell surface receptors and inducing intracellular signaling. In this review, we discuss certain leukocyte functions, namely neutrophil extracellular traps formation and cytokine release, and the inhibition of these processes by activated protein C.
固有免疫细胞是宿主防御反应的重要组成部分,通过释放促炎细胞因子或形成中性粒细胞胞外陷阱来促进炎症反应。虽然这些过程对于抵御感染因子或损伤很重要,但异常激活会加剧病理性炎症疾病。因此,了解限制中性粒细胞胞外陷阱形成和细胞因子释放的调节机制对于靶向治疗病理性疾病具有重要意义。活化蛋白C是一种内源性丝氨酸蛋白酶,具有抗凝活性以及抗炎和细胞保护功能,后者是通过结合细胞表面受体并诱导细胞内信号传导来介导的。在本综述中,我们讨论了某些白细胞功能,即中性粒细胞胞外陷阱形成和细胞因子释放,以及活化蛋白C对这些过程的抑制作用。