Molecular characterization and expression analysis of three membrane-bound complement regulatory protein isoforms in the ginbuna crucian carp Carassius auratus langsdorfii

被引:8
|
作者
Nur, Indriyani [1 ]
Harada, Hikari [1 ]
Tsujikura, Masakazu [1 ]
Somamoto, Tomonori [1 ]
Nakao, Miki [1 ]
机构
[1] Kyushu Univ, Marine Biochem Lab, Dept Biosci & Biotechnol, Grad Sch Bioresource & Bioenvironm Sci,Higashi Ku, Fukuoka 8128581, Japan
关键词
Membrane-bound complement regulatory protein; Short consensus repeats; Ginbuna crucian carp; Teleost; Isoform; COFACTOR PROTEIN; PLASMA-PROTEIN; CD46; IDENTIFICATION; CLONING; SYSTEM; MCP; ACTIVATION; CONVERTASE; EVOLUTION;
D O I
10.1016/j.fsi.2013.08.002
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Regulators of complement activation (RCA) play a role in protecting cells from excessive complement activation in humans. cDNA corresponding to three isoforms of teleost membrane-bound RCA protein (gTecrem) have been identified in the ginbuna crucian carp. gTecrem-1 consists of seven short consensus repeats (SCRs), whereas gTecrem-2 and gTecrem-3 have four SCRs. While gTecrem-1 possesses a tyrosine phosphorylation site in its cytoplasmic region, gTecrem-2 and gTecrem-3 lack the site. Tissue distribution analysis showed that gTecrem-1 and gTecrem-2 mRNAs were expressed in almost all tissues examined, whereas gTecrem-2 expression was not significantly detected in gill, liver, or intestine. Furthermore, analysis showed that gTecrem-1 was expressed in both peripheral blood leukocytes (PBLs) and erythrocytes and was also expressed in T cell subsets such as CD4(+), CD8(+) T cells, and IgM(+) B cells. gTecrem-2 expression was not detected in either PBLs or erythrocytes, whereas gTecrem-3 was expressed only in erythrocytes. These results suggested that gTecrem isoforms may serve different functional roles; gTecrem-1, which is expressed in T cells and possesses a tyrosine phosphorylation site, may act as a complement regulator and a cellular receptor in adaptive immunity. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1333 / 1337
页数:5
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