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Iron-metabolic function and potential antibacterial role of Hepcidin and its correlated genes (Ferroportin 1 and Transferrin Receptor) in Turbot (Scophthalmus maximus)

文献类型: 外文期刊

作者: Yang, Chang-Geng 1 ; Liu, Shan-Shan 1 ; Sun, Bing 1 ; Wang, Xian-Li 4 ; Wang, Na 1 ; Chen, Song-Lin 1 ;

作者机构: 1.Chinese Acad Fisheries Sci, Yellow Sea Fisheries Res Inst, Qingdao 266071, Shandong, Peoples R China

2.Chinese Acad Fishery Sci, Yangtze River Fisheries Res Inst, Wuhan 430223, Peoples R China

3.Dalian Fisheries Univ, Minist Agr, Key Lab Mariculture & Biotechnol, Dalian 116023, Peoples R China

4.Tongji Univ, Sch Med, Stem Cell Res Ctr, Translat Ctr Stem Cell Res,Tongji Hosp, Shanghai 200065, Peoples R China

关键词: Hepcidin;Iron-metabolism;Turbot;NF-kappa B;Immunity

期刊名称:FISH & SHELLFISH IMMUNOLOGY ( 影响因子:4.581; 五年影响因子:4.851 )

ISSN: 1050-4648

年卷期: 2013 年 34 卷 3 期

页码:

收录情况: SCI

摘要: Antimicrobial peptide plays an important role in fish immunity. The small molecular antimicrobial peptide Hepcidin in turbot was studied and reported in this paper. The Ferroportin 1 (FPN1) and Transferrin Receptor (TFR) genes, which are related to Hepcidin, were cloned in turbot. The characteristics of Hepcidin and its related genes were studied, including an analysis of the expression patterns and cloning of the Hepcidin promoter, the relationship between Hepcidin and NF-kappa B and the regulation of iron-metabolism. The results showed that the promoter of SmHepcidin contains the binding sites of NF-kappa B, and NF-kappa B may directly or indirectly receive feedback signals from SmHepcidin. In the liver, spleen and kidney, in which there was an increased SmHepcidin expression level, SmFPN1 dramatically decreased and SmTFR was also either decreased or exhibited no obvious change after bacterial/viral infection and an injection of exogenous Hepcidin protein. RNAi experiments in turbot kidney cells confirmed the expression changes of these gene patterns. Furthermore, the administration of exogenous Hepcidin protein, which regulates the level of chelatable iron in cells, further confirmed the function of Hepcidin in iron metabolism. It is speculated that the rapidly increased expression of SmHepcidin may induce changes in the expression of related genes, and that the in vivo chelatable iron concentration which participates in the antibacterial process was also changed when exogenous pathogens are present in turbot. It is suggested that SmHepcidin plays a defensive role against pathogenic infection. (C) 2012 Elsevier Ltd. All rights reserved.

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