Chemokine receptor CXCR3 in turbot (Scophthalmus maximus): cloning, characterization and its responses to lipopolysaccharide

被引:21
作者
Chen, Yadong [1 ,2 ]
Zhou, Shuhong [1 ]
Jiang, Zhiqiang [1 ]
Wang, Xiuli [1 ]
Liu, Yang [1 ]
机构
[1] Dalian Ocean Univ, Key Lab Mariculture & Stock Enhancement North Chi, Minist Agr, 52 Heishijiao St, Dalian 116023, Liaoning, Peoples R China
[2] Chinese Acad Fishery Sci, Yellow Sea Fisheries Res Inst, Qingdao 266071, Peoples R China
关键词
Chemokine receptor; Immune response; Lipopolysaccharide; Scophthalmus maximus; CHRONIC HEPATITIS-C; EXPRESSION ANALYSIS; MOLECULAR-CLONING; GENE CONVERSION; T-CELLS; I-TAC; TELEOST FISH; RECRUITMENT; CCR5; LIVER;
D O I
10.1007/s10695-015-0167-1
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
Chemokine (C-X-C motif) receptor 3, a member of the G protein-coupled receptors superfamily, regulates the responses of many immune responses. In this experiment, we cloned and characterized the cDNA of CXCR3 in Scophthalmus maximus (turbot). A 5'-UTR of 216-bp, a 259-bp 3'-UTR with a poly (A) tail and a 1089-bp CDS encoding 362 amino acids form the cDNA of CXCR3, which is 1564-bp long. Phylogenetic analyses indicated that turbot CXCR3 shared a high similarity with other CXCR3s and shared more similarity with CXCR5 than the other subfamilies of chemokines. The CXCR3 protein in turbot showed the highest similarity with the CXCR3b from rainbow trout (44.5 %), which indicated that this CXCR3 gene/protein may be a CXCR3b isoform. Quantitative real-time PCR analysis showed that CXCR3 transcripts were constitutively expressed in all the tissues of the non-injected turbot used in this study, with the highest expression occurring in blood. Several immune-related tissues of fish, such as the spleen, head kidney, liver and blood, tissues, which were abundant of lymphocyte, were investigated in this study. CXCR3 gene was expressed at the highest level in blood than the other tested tissues. The injection experiment suggested that the CXCR3 expression level after LPS injection was significantly up-regulated in all immune-related tissues in turbot. These results improve our understanding of the functions of CXCR3 in the turbot immune response.
引用
收藏
页码:659 / 671
页数:13
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