The complement system in teleosts

被引:557
作者
Holland, MCH [1 ]
Lambris, JD [1 ]
机构
[1] Univ Penn, Dept Pathol & Lab Med, Stellar Chance Labs 401, Philadelphia, PA 19014 USA
关键词
complement; innate; immunity; fish;
D O I
10.1006/fsim.2001.0408
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Complement, an important component of the innate immune system, is comprised of about 35 individual proteins. In mammals, activation of complement results in the generation of activated protein fragments that play a role in microbial killing, phagocytosis, inflammatory reactions, immune complex clearance, and antibody production. Fish appear to possess activation pathways similar to those in mammals, and the fish complement proteins identified thus far show many homologies to their mammalian counterparts. Because information about complement proteins, regulatory proteins, and complement receptors in fish is far from complete, it is unclear whether all the complement functions that have been identified in mammals also occur in fish. However, it has been clearly demonstrated that fish complement can lyse foreign cells and opsonise foreign organisms for destruction by phagocytes. There are also indications that complement fragments participate in inflammatory reactions. Fish possess multiple isoforms of several complement proteins, such as C3 and factor B. It has been hypothesised that the function of this diversity in complement proteins serves to expand their innate immune recognition capacity and response. Understanding the functions of complement in fish and the roles the individual proteins, including the various isoforms, play in host defence, is important not only for understanding the evolution of this system but also for the development of new strategies in fish health management. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:399 / 420
页数:22
相关论文
共 132 条
[21]  
Dodds AW, 1998, IMMUNOL REV, V166, P15
[22]   Isolation and initial characterisation of complement components C3 and C4 of the nurse shark and the channel catfish [J].
Dodds, AW ;
Smith, SL ;
Levine, RP ;
Willis, AC .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 1998, 22 (02) :207-216
[23]  
dos Remedies NJ, 1999, DEV COMP IMMUNOL, V23, P1, DOI 10.1016/S0145-305X(98)00049-4
[24]   HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ACTIVATES THE CLASSICAL PATHWAY OF COMPLEMENT BY DIRECT C1-BINDING THROUGH SPECIFIC SITES IN THE TRANSMEMBRANE GLYCOPROTEIN-GP41 [J].
EBENBICHLER, CF ;
THIELENS, NM ;
VORNHAGEN, R ;
MARSCHANG, P ;
ARLAUD, GJ ;
DIERICH, MP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (06) :1417-1424
[25]  
Endo Y, 1998, J IMMUNOL, V161, P4924
[26]  
Erdei A, 1997, EXP CLIN IMMUNOGENET, V14, P16
[27]   Elements of immunity - The instructive role of innate immunity in the acquired immune response [J].
Fearon, DT ;
Locksley, RM .
SCIENCE, 1996, 272 (5258) :50-54
[28]   Cloning and purification of the rainbow trout fifth component of complement (C5) [J].
Franchini, S ;
Zarkadis, IK ;
Sfyroera, G ;
Sahu, A ;
Moore, WT ;
Mastellos, D ;
LaPatra, SE ;
Lambris, JD .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2001, 25 (5-6) :419-430
[29]  
FUJII T, 1992, J IMMUNOL, V148, P117
[30]  
Gadjeva M, 1998, J IMMUNOL, V161, P985