Programmed cell clearance

被引:86
作者
Fadeel, B [1 ]
机构
[1] Karolinska Inst, Inst Environm Med, Div Toxicol, S-17177 Stockholm, Sweden
关键词
apoptosis; phagocytosis; macrophage; inflammation; autoimmune disease;
D O I
10.1007/s00018-003-3145-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis, a physiological process of self-annihilation, is essential during development and for the maintenance of tissue homeostasis. Considerable efforts have been made in recent years to elucidate the molecular mechanisms that govern this mode of cellular demise; however, the subsequent recognition and removal of apoptotic corpses by neighboring phagocytes has received less attention. Nevertheless, macrophage engulfment of apoptotic cells is known to be important in the remodeling of tissues, and contributes to the resolution of inflammation through the removal of effete cells prior to the release of noxious cellular constituents. Moreover, apoptotic cells are a potential source of self-antigens, and clearance of cell corpses is thought to preclude the induction of autoimmune responses. The view is thus emerging that tissue homeostasis is dependent not only on the balance between mitosis and apoptosis, but also on the rate of apoptosis versus that of cell clearance. This review aims to discuss the mechanisms and consequences of macrophage recognition and disposal of apoptotic cells, a process which will be referred to as programmed cell clearance.
引用
收藏
页码:2575 / 2585
页数:11
相关论文
共 144 条
[31]  
DUVALL E, 1985, IMMUNOLOGY, V56, P351
[32]   A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD [J].
Enari, M ;
Sakahira, H ;
Yokoyama, H ;
Okawa, K ;
Iwamatsu, A ;
Nagata, S .
NATURE, 1998, 391 (6662) :43-50
[33]   Apoptosis in human disease: A new skin for the old ceremony? [J].
Fadeel, B ;
Orrenius, S ;
Zhivotovsky, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 266 (03) :699-717
[34]   Apoptosis and macrophage clearance of neutrophils: regulation by reactive oxygen species [J].
Fadeel, B ;
Kagan, VE .
REDOX REPORT, 2003, 8 (03) :143-150
[35]   Involvement of caspases in neutrophil apoptosis:: Regulation by reactive oxygen species [J].
Fadeel, B ;
Åhlin, A ;
Henter, JI ;
Orrenius, S ;
Hampton, MB .
BLOOD, 1998, 92 (12) :4808-4818
[36]  
FADOK VA, 1992, J IMMUNOL, V149, P4029
[37]   A receptor for phosphatidylserine-specific clearance of apoptotic cells [J].
Fadok, VA ;
Bratton, DL ;
Rose, DM ;
Pearson, A ;
Ezekewitz, RAB ;
Henson, PM .
NATURE, 2000, 405 (6782) :85-90
[38]   Loss of phospholipid asymmetry and surface exposure of phosphatidylserine is required for phagocytosis of apoptotic cells by macrophages and fibroblasts [J].
Fadok, VA ;
de Cathelineau, A ;
Daleke, DL ;
Henson, PM ;
Bratton, DL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (02) :1071-1077
[39]  
FADOK VA, 1992, J IMMUNOL, V148, P2207
[40]   Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-β, PGE2, and PAF [J].
Fadok, VA ;
Bratton, DL ;
Konowal, A ;
Freed, PW ;
Westcott, JY ;
Henson, PM .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (04) :890-898