Clearance of apoptotic cells: Getting rid of the corpses

被引:448
作者
Lauber, K [1 ]
Blumenthal, SG [1 ]
Waibel, M [1 ]
Wesselborg, S [1 ]
机构
[1] Univ Tubingen, Dept Internal Med 1, D-72076 Tubingen, Germany
关键词
D O I
10.1016/S1097-2765(04)00237-0
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
The efficient elimination of apoptotic cells is crucial for tissue homeostasis in multicellular organisms. Secreted "find-me," exposed "eat-me," and lacking "don't-eat-me" signals comprise the central elements of apoptotic cell removal, thus preventing the release of intracellular contents into the surrounding tissue. This is of special importance, as there is growing evidence that the onset of autoimmune disorders can be linked to the inefficient removal of apoptotic cells. This review focuses on the signals displayed by apoptotic cells, the bridging and receptor molecules on the phagocyte, and is intended to present a simplified model of the phagocytic synapse. Additionally, the recent discovery of lysophosphatidylcholine functioning as soluble attraction signal is discussed in the general context of apoptotic cell clearance.
引用
收藏
页码:277 / 287
页数:11
相关论文
共 89 条
[61]   Role for the class A macrophage scavenger receptor in the phagocytosis of apoptotic thymocytes in vitro [J].
Platt, N ;
Suzuki, H ;
Kurihara, Y ;
Kodama, T ;
Gordon, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) :12456-12460
[62]  
Price BE, 1996, J IMMUNOL, V157, P2201
[63]   LYSOPHOSPHATIDYLCHOLINE - A CHEMOTACTIC FACTOR FOR HUMAN-MONOCYTES AND ITS POTENTIAL ROLE IN ATHEROGENESIS [J].
QUINN, MT ;
PARTHASARATHY, S ;
STEINBERG, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (08) :2805-2809
[64]   OXIDATIVELY MODIFIED LOW-DENSITY LIPOPROTEINS - A POTENTIAL ROLE IN RECRUITMENT AND RETENTION OF MONOCYTE MACROPHAGES DURING ATHEROGENESIS [J].
QUINN, MT ;
PARTHASARATHY, S ;
FONG, LG ;
STEINBERG, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (09) :2995-2998
[65]   Phagocytosis promotes programmed cell death in C-elegans [J].
Reddien, PW ;
Cameron, S ;
Horvitz, HR .
NATURE, 2001, 412 (6843) :198-202
[66]   CED-2/Crkll and CED-10/Rac control phagocytosis and cell migration in Caenorhabditis elegans [J].
Reddien, PW ;
Horvitz, HR .
NATURE CELL BIOLOGY, 2000, 2 (03) :131-136
[67]   CD36 GENE-TRANSFER CONFERS CAPACITY FOR PHAGOCYTOSIS OF CELLS UNDERGOING APOPTOSIS [J].
REN, Y ;
SILVERSTEIN, RL ;
ALLEN, J ;
SAVILL, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (05) :1857-1862
[68]   Autoantigens as substrates for apoptotic proteases: implications for the pathogenesis of systemic autoimmune disease [J].
Rosen, A ;
Casciola-Rosen, L .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (01) :6-12
[69]   The selective engulfment of apoptotic bodies by dendritic cells is mediated by the alpha v beta 3 integrin and requires intracellular and extracellular calcium [J].
Rubartelli, A ;
Poggi, A ;
Zocchi, MR .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (08) :1893-1900
[70]   LYSOPHOSPHATIDYLCHOLINE - A CHEMOATTRACTANT TO HUMAN T-LYMPHOCYTES [J].
RYBORG, AK ;
DELEURAN, B ;
THESTRUPPEDERSEN, K ;
KRAGBALLE, K .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1994, 286 (08) :462-465