Chelombitko M A, Fedorov A V, Ilyinskaya O P, Zinovkin R A, Chernyak B V
Lomonosov Moscow State University, Faculty of Biology, Moscow, 119991, Russia.
Biochemistry (Mosc). 2016 Dec;81(12):1564-1577. doi: 10.1134/S000629791612018X.
Mast cells are a heterogeneous multifunctional cellular population that promotes connective tissue homeostasis by slow release of biologically active substances, affecting primarily the permeability of vessels and vascular tone, maintenance of electrolyte and water balance, and composition of the extracellular matrix. Along with this, they can rapidly release inflammatory mediators and chemotactic factors that ensure the mobilization of effector innate immune cells to fight against a variety of pathogens. Furthermore, they play a key role in initiation of allergic reactions. Aggregation of high affinity receptors to IgE (FcεRI) results in rapid degranulation and release of inflammatory mediators. It is known that reactive oxygen species (ROS) participate in intracellular signaling and, in particular, stimulate production of several proinflammatory cytokines that regulate the innate immune response. In this review, we focus on known molecular mechanisms of FcεRI-dependent activation of mast cells and discuss the role of ROS in the regulation of this pathway.
肥大细胞是一类异质性多功能细胞群体,通过缓慢释放生物活性物质促进结缔组织稳态,主要影响血管通透性和血管张力、维持电解质和水平衡以及细胞外基质的组成。与此同时,它们能够快速释放炎症介质和趋化因子,确保效应性固有免疫细胞动员起来对抗各种病原体。此外,它们在过敏反应的启动中起关键作用。高亲和力IgE受体(FcεRI)聚集导致炎症介质的快速脱颗粒和释放。已知活性氧(ROS)参与细胞内信号传导,特别是刺激几种调节固有免疫反应的促炎细胞因子的产生。在本综述中,我们聚焦于FcεRI依赖性肥大细胞激活的已知分子机制,并讨论ROS在该途径调节中的作用。