传出细胞增多
炎症
吞噬作用
巨噬细胞
细胞生物学
细胞凋亡
免疫学
生物
自身免疫
免疫系统
体外
遗传学
作者
Ioannis Kourtzelis,George Hajishengallis,Triantafyllos Chavakis
标识
DOI:10.3389/fimmu.2020.00553
摘要
Efficient inflammation resolution is important not only for the termination of the inflammatory response but also for the restoration of tissue integrity. An integral process to resolution of inflammation is the phagocytosis of dying cells by macrophages, known as efferocytosis. This function is mediated by a complex and well-orchestrated network of interactions amongst specialized phagocytic receptors, bridging molecules, as well as ‘find-me’ and ‘eat-me’ signals. Efferocytosis serves not only as a waste disposal mechanism (clearance of the apoptotic cells) but also promotes a pro-resolving phenotype in efferocytic macrophages and thereby termination of inflammation. Alterations in cellular metabolism are critical for shaping the phenotype and function of efferocytic macrophages, thus, representing an important determinant of macrophage plasticity. Impaired efferocytosis can result in inflammation-associated pathologies or autoimmunity. The present mini review summarizes current knowledge regarding the mechanisms regulating macrophage efferocytosis during clearance of inflammation.
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