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Duck RIG-I CARD Domain Induces the Chicken IFN-β by Activating NF-kB

机译:鸭子钻机I卡片域通过激活NF-KB诱导鸡IFN-β

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Retinoic acid-inducible gene I- (RIG-I-) like receptors (RLRs) have recently been identified as cytoplasmic sensors for viral RNA. RIG-I, a member of RLRs family, plays an important role in innate immunity. Although previous investigations have proved that RIG-I is absent in chickens, it remains largely unknown whether the chicken can respond to RIG-I ligand. In this study, the eukaryotic expression vectors encoding duRIG-I full length (duck RIG-I, containing all domains), duRIG-I N-terminal (containing the two caspase activation and recruitment domain, CARDs), and duRIG-I C-terminal (containing helicase and regulatory domains) labeled with 6*His tags were constructed successfully and detected by western blotting. Luciferase reporter assay and enzyme-linked immunosorbent assay (ELISA) detected the duRIG-I significantly activated NF-kB and induced the expression of IFN-β when polyinosinic-polycytidylic acid (poly[I:C], synthetic double-stranded RNA) challenges chicken embryonic fibroblasts cells (DF1 cells), while the duRIG-I was inactive in the absence of poly[I:C]. Further analysis revealed that the CARDs (duRIG-I-N) induced IFN-β production regardless of the presence of poly[I:C], while the CARD-lacking duRIG-I (duRIG-I-C) was not capable of activating downstream signals. These results indicate that duRIG-I CARD domain plays an important role in the induction of IFN-β and provide a basis for further studying the function of RIG-I in avian innate immunity.
机译:最近已被鉴定为病毒RNA的细胞质传感器(RLR)等视黄酸 - 诱导基因I-(RLRS)。 RIN-I是RLRS系列的成员,在先天免疫中起着重要作用。虽然先前的调查证明,钻石I在鸡中缺席,但它仍然很大程度上未知鸡肉是否可以响应钻井平台。在本研究中,编码DURIG-I全长的真核表达载体(鸭子钻机-I,包含所有域),DURIG-I N终端(包含两个Caspase激活和招聘领域,卡)和DURIG-I C-用6 *标记的末端(含有螺旋酶和调节结构域)成功构建并通过Western印迹进行检测。荧光素酶报告测定和酶联免疫吸附测定(ELISA)检测到DURIG-I显着活化的NF-KB,并在多胞聚环酸(Poly [I:C],合成双链RNA)挑战时诱导IFN-β的表达鸡胚胎成纤维细胞(DF1细胞),而DURIG-I在没有聚[i:c]的情况下无活性。进一步的分析表明,无论存在多[I:C]的存在,卡(DURIG-I-N)诱导IFN-β的产生,而缺陷的DURIG-I(DURIG-I-C)不能激活下游信号。这些结果表明,DURIG-I卡片域在IFN-β的诱导中起着重要作用,并为进一步研究RIG-I在禽类疫苗中提供的基础。

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