Apoptosis and Clearance of Apoptotic Cells

被引:769
作者
Nagata, Shigekazu [1 ]
机构
[1] Osaka Univ, Initiat Immunol Frontier Res Ctr, World Premier Int Res Ctr, Lab Biochem & Immunol, Osaka 5650871, Japan
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 36 | 2018年 / 36卷
关键词
apoptosis; efferocytosis; macrophages; phosphatidylserine; flippase; scramblase; caspase; TIM4; TAM receptors; RECEPTOR TYROSINE KINASES; GLYCATION END-PRODUCTS; RED-BLOOD-CELLS; PLASMA-MEMBRANE PHOSPHATIDYLSERINE; PHOSPHOLIPID SCRAMBLASE ACTIVITY; GLOBULE-EGF FACTOR-8; ACTIVATED PROTEIN-C; SOLUBLE FAS LIGAND; GROWTH-ARREST; TRANSBILAYER MOVEMENT;
D O I
10.1146/annurev-immunol-042617-053010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The human body generates 10-100 billion cells every day, and the same number of cells die to maintain homeostasis in our body. Cells infected by bacteria or viruses also die. The cell death that occurs under physiological conditions mainly proceeds by apoptosis, which is a noninflammatory, or silent, process, while pathogen infection induces necroptosis or pyroptosis, which activates the immune system and causes inflammation. Dead cells generated by apoptosis are quickly engulfed by macrophages for degradation. Caspases are a large family of cysteine proteases that act in cascades. A cascade that leads to caspase 3 activation mediates apoptosis and is responsible for killing cells, recruiting macrophages, and presenting an "eat me" signal(s). When apoptotic cells are not efficiently engulfed by macrophages, they undergo secondary necrosis and release intracellular materials that represent a damage-associated molecular pattern, which may lead to a systemic lupus-like autoimmune disease.
引用
收藏
页码:489 / 517
页数:29
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