C1q and tumor necrosis factor superfamily: modularity and versatility

被引:372
作者
Kishore, U [1 ]
Gaboriaud, C
Waters, P
Shrive, AK
Greenhough, TJ
Reid, KBM
Sim, RB
Arlaud, GJ
机构
[1] Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Oxford OX3 9DS, England
[2] Univ Giessen, Inst Med Microbiol, D-35392 Giessen, Germany
[3] Univ Grenoble 1, CEA, CNRS,Lab Cristallog & Cristallogenese Prot, Inst Biol Struct Jean Pierre Ebel, F-38027 Grenoble, France
[4] Univ Grenoble 1, CEA, CNRS,Lab Enzymol Mol, Inst Biol Struct Jean Pierre Ebel, F-38027 Grenoble, France
[5] Univ Keele, Sch Life Sci, Keele ST5 5BG, Staffs, England
[6] Univ Oxford, Dept Biochem, MRC, Immunochem Unit, Oxford OX1 3QU, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1016/j.it.2004.08.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
C1q is the target recognition protein of the classical complement pathway and a major connecting link between innate and acquired immunity. As a charge pattern recognition molecule of innate immunity, C1q can engage a broad range of ligands via its globular (gC1q) domain and modulate immune cells, probably via its collagen region. The gC1q signature domain, also found in many non-complement proteins, has a compact jelly-roll beta-sandwich fold similar to that of the multifunctional tumor necrosis factor (TNF) ligand family. The members of this newly designated 'C1q and TNF superfamily' are involved in processes as diverse as host defense, inflammation, apoptosis, autoimmunity, cell differentiation, organogenesis, hibernation and insulin-resistant obesity. This review is an attempt to draw structural and functional parallels between the members of the C1q and TNF superfamily.
引用
收藏
页码:551 / 561
页数:11
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