cynoglossus semilaevis isg15 a secreted cytokine-like protein that stimulates antiviral immune response in a lrgg motif-dependent mannercynoglossus semilaevis isg15 cytokine-like分泌蛋白刺激抗病毒免疫反应在lrgg motif-dependent方式.pdfVIP

cynoglossus semilaevis isg15 a secreted cytokine-like protein that stimulates antiviral immune response in a lrgg motif-dependent mannercynoglossus semilaevis isg15 cytokine-like分泌蛋白刺激抗病毒免疫反应在lrgg motif-dependent方式.pdf

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cynoglossus semilaevis isg15 a secreted cytokine-like protein that stimulates antiviral immune response in a lrgg motif-dependent mannercynoglossus semilaevis isg15 cytokine-like分泌蛋白刺激抗病毒免疫反应在lrgg motif-dependent方式

Cynoglossus semilaevis ISG15: A Secreted Cytokine-Like Protein That Stimulates Antiviral Immune Response in a LRGG Motif-Dependent Manner 1,2 1 1 1 Wei Wang , Min Zhang , Zhi-zhong Xiao , Li Sun * 1 Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, China, 2 Graduate University of the Chinese Academy of Sciences, Beijing, China Abstract ISG15 is an ubiquitin-like protein that is induced rapidly by interferon stimulation. Like ubiquitin, ISG15 forms covalent conjugates with its target proteins in a process called ISGylation, which in mammals is known to play a role in antiviral immunity. In contrast to mammalian ISG15, the function of teleost ISG15 is unclear. In this study, we identified and analyzed the function of an ISG15 homologue, CsISG15, from tongue sole (Cynoglossus semilaevis). CsISG15 is composed of 162 residues and possesses two tandem ubiquitin-like domains and the highly conserved LRGG motif found in all known ISG15. Expression of CsISG15 occurred in a wide range of tissues and was upregulated in kidney and spleen by viral and bacterial infection. In vitro study with primary head kidney (HK) lymphocytes showed that megalocytivirus infection caused induction of CsISG15 expression and extracellular release of CsISG15 protein. Purified recombinant CsISG15 (rCsISG15) activated HK macrophages and enhanced the expression of immune genes in HK lymphocytes, both these effects, however, were significantly reduced when the conserved LRGG sequence was mutated to LAAG. Further study showed that the presence of rCsISG15 during megalocytivirus infection of HK lymphocytes reduced intracellular viral load, whereas antibody blocking of CsISG15 enhanced viral infection. Likewise, interfer

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