Clearance of apoptotic neutrophils and resolution of inflammation

被引:393
作者
Greenlee-Wacker, Mallary C. [1 ]
机构
[1] Univ Iowa, Dept Internal Med, Roy J & Lucille A Carver Coll Med, Inflammat Program,Vet Adm Med Ctr, Iowa City, IA 52242 USA
关键词
apoptosis; efferocytosis; infection; inflammation; macrophages; neutrophil; RECEPTOR-MEDIATED PHAGOCYTOSIS; PROGRAMMED CELL-DEATH; MER TYROSINE KINASE; FC-GAMMA-RIII; VITRONECTIN RECEPTOR; MACROPHAGE PHAGOCYTOSIS; DENDRITIC CELLS; PHOSPHATIDYLSERINE RECEPTOR; DEPENDENT PHAGOCYTOSIS; PPAR-GAMMA;
D O I
10.1111/imr.12453
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The engulfment of apoptotic cells by phagocytes, a process referred to as efferocytosis, is essential for maintenance of normal tissue homeostasis and a prerequisite for the resolution of inflammation. Neutrophils are the predominant circulating white blood cell in humans, and contain an arsenal of toxic substances that kill and degrade microbes. Neutrophils are short-lived and spontaneously die by apoptosis. This review will highlight how the engulfment of apoptotic neutrophils by human phagocytes occurs, how heterogeneity of phagocyte populations influences efferocytosis signaling, and downstream consequences of efferocytosis. The efferocytosis of apoptotic neutrophils by macrophages promotes anti-inflammatory signaling, prevents neutrophil lysis, and dampens immune responses. Given the immunomodulatory properties of efferocytosis, understanding pathways that regulate and enhance efferocytosis could be harnessed to combat infection and chronic inflammatory conditions.
引用
收藏
页码:357 / 370
页数:14
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