Eaten alive! Cell death by primary phagocytosis: 'phagoptosis'

被引:286
作者
Brown, Guy C. [1 ]
Neher, Jonas J. [1 ]
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
基金
英国惠康基金;
关键词
phagocytosis; apoptosis; cell death; turnover; inflammation; clearance; APOPTOTIC CELLS; PHOSPHATIDYLSERINE EXTERNALIZATION; CAENORHABDITIS-ELEGANS; NEURONAL DEATH; SURFACE EXPOSURE; SIALIC-ACID; STEM-CELLS; T-CELLS; CLEARANCE; ENGULFMENT;
D O I
10.1016/j.tibs.2012.05.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Phagoptosis, also called primary phagocytosis, is a recently recognised form of cell death caused by phagocytosis of viable cells, resulting in their destruction. It is provoked by exposure of 'eat-me' signals and/or loss of 'don't-eat-me' signals by viable cells, causing their phagocytosis by phagocytes. Phagoptosis mediates turnover of erythrocytes, neutrophils and other cells, and thus is quantitatively one of the main forms of cell death in the body. It defends against pathogens and regulates inflammation and immunity. However, recent results indicate that inflamed microglia eat viable brain neurons in models of neurodegeneration, and cancer cells can evade phagocytosis by expressing a 'don't-eat-me' signal, suggesting that too much or too little phagoptosis can contribute to pathology. This review provides an overview of the molecular signals that regulate phagoptosis and the physiological and pathological circumstances in which it has been observed.
引用
收藏
页码:325 / 332
页数:8
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