Beyond lysis: how complement influences cell fate

被引:142
作者
Cole, DS [1 ]
Morgan, BP [1 ]
机构
[1] Univ Wales Coll Med, Dept Med Biochem & Immunol, Cardiff CF14 4XN, S Glam, Wales
关键词
apoptosis; C5a; cell death; complement; membrane attack complex; non-lethal effects;
D O I
10.1042/CS20020362
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Complement is a central component of the innate immune system involved in protection against pathogens. For many years, complement has been known to cause death of targets, either indirectly by attracting and activating phagocytes or directly by formation of a membrane pore, the membrane attack complex. More recently, it has been recognized that complement may cause other 'non-classical' effects that may not directly be aimed at killing of pathogens. Products of complement activation collaborate with the adaptive immune system to enhance responses to antigens. The membrane attack complex of complement, apart from lysing cells, can also trigger diverse events in target cells that include cell activation, proliferation, resistance to subsequent complement attack and either resistance to, or induction of, apoptosis. Various complement products play important roles in signalling for clearance by phagocytes of apoptotic self cells. Here we review some of these non-classical activities of complement and stress the roles that they may play in maintaining the integrity of the organism.
引用
收藏
页码:455 / 466
页数:12
相关论文
共 105 条
[71]   EFFECTS OF CA2+ DEREGULATION ON MITOCHONDRIAL-MEMBRANE POTENTIAL AND CELL VIABILITY IN NUCLEATED CELLS FOLLOWING LYRIC COMPLEMENT ATTACK [J].
PAPADIMITRIOU, JC ;
PHELPS, PC ;
SHIN, ML ;
SMITH, MW ;
TRUMP, BF .
CELL CALCIUM, 1994, 15 (03) :217-227
[72]  
PAPADIMITRIOU JC, 1991, J IMMUNOL, V147, P212
[73]   Complement activates the c-Jun N-terminal kinase/stress-activated protein kinase in glomerular epithelial cells [J].
Peng, HW ;
Takano, T ;
Papillon, J ;
Bijian, K ;
Khadir, A ;
Cybulsky, AV .
JOURNAL OF IMMUNOLOGY, 2002, 169 (05) :2594-2601
[74]   Glutamate excitotoxicity in a model of multiple sclerosis [J].
Pitt, D ;
Werner, P ;
Raine, CS .
NATURE MEDICINE, 2000, 6 (01) :67-70
[75]   MEMBRANE ATTACK BY COMPLEMENT [J].
PODACK, ER ;
TSCHOPP, J .
MOLECULAR IMMUNOLOGY, 1984, 21 (07) :589-603
[76]   METHODS FOR ASSESSING COMPLEMENT ACTIVATION IN THE CLINICAL IMMUNOLOGY LABORATORY [J].
PORCEL, JM ;
PEAKMAN, M ;
SENALDI, G ;
VERGANI, D .
JOURNAL OF IMMUNOLOGICAL METHODS, 1993, 157 (1-2) :1-9
[77]   Immunohistochemical localization of cytokines, C5b-9 and ICAM-1 in peripheral nerve of Guillain-Barre Syndrome [J].
Putzu, GA ;
Figarella-Branger, D ;
Bouvier-Labit, C ;
Liprandi, A ;
Bianco, N ;
Pellissier, JF .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2000, 174 (01) :16-21
[78]   SUBLYTIC COMPLEMENT ATTACK PROTECTS TUMOR-CELLS FROM LYTIC DOSES OF ANTIBODY AND COMPLEMENT [J].
REITER, Y ;
CIOBOTARIU, A ;
FISHELSON, Z .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (05) :1207-1213
[79]  
REITER Y, 1995, J IMMUNOL, V155, P2203
[80]   COMPLEMENT MEMBRANE ATTACK COMPLEXES INDUCE IN HUMAN LEUKEMIC-CELLS RAPID EXPRESSION OF LARGE PROTEINS (L-CIP) [J].
REITER, Y ;
FISHELSON, Z .
MOLECULAR IMMUNOLOGY, 1992, 29 (06) :771-781