首页> 外文期刊>Developmental and Comparative Immunology: Ontogeny, Phylogeny, Aging: The Official Journal of the International Society of Developmental and Comparative Immunology >Identification, characterization and immunological response analysis of stimulator of interferon gene (STING) from grass carp Ctenopharyngodon idella
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Identification, characterization and immunological response analysis of stimulator of interferon gene (STING) from grass carp Ctenopharyngodon idella

机译:草鱼Ctenopharyngodon idella干扰素基因(STING)刺激物的鉴定,表征和免疫应答分析

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摘要

Stimulator of interferon gene (STING), an important adapter responsible for RLR pathway, plays a pivotal role in both viral RNA- and DNA-triggered induction of IFNs in mammals. To understand the roles of STING in piscine immune system, STING gene (CiSTING) was identified from grass carp (Ctenopharyngodon idella). The genomic sequence of CiSTING was of 8548 base pairs (bp), including 899 bp 50 flank region, 7 exons and 6 introns. Promoter region was predicted and promoter activity was verified. The CiSTING cDNA was of 1358 bp with an open reading frame of 1185 bp, encoding a polypeptide of 394 amino acids with a signal peptide and three transmembrane motifs in the N-terminal region. mRNA expression of CiSTING was widespread in fifteen tissues investigated, and was up-regulated by GCRV in vivo and in vitro. Meanwhile, the transcription of CiSTING was inhibited at early stage, and then up-regulated at late phase upon poly(I:C) or PGN stimulation in vitro. Interestingly, CiSTING had little impact on LPS in vitro. In CiSTING over-expression cells, CiTBK1, CiIRF3 and CiIRF7 were significantly up-regulated post GCRV or viral/bacterial PAMPs stimulation. In addition, post GCRV or PGN stimulation, the transcription of CiIFN-I was remarkably inhibited while CiMx1 was up-regulated; as for poly(I:C) stimulation, mRNA expressions of CiIFN-I and CiMx1 were inhibited at early stage while enhanced at late phrase; after LPS stimulation, both CiIFN-I and CiMx1 were inhibited. Furthermore, antiviral activity of CiSTING was manifested by the inhibition of GCRV yield. Taken together, these results demonstrated that CiSTING may be involved in board innate immune responses via the TBK1-IRF3/IRF7 cascade, responding to not only dsRNA analogue in an IFN-dependent pathway, but also virus and bacterial PAMPs in an IFNindependent pathway. This study provided novel insights into the essential role of STING in innate immunity.
机译:干扰素基因的刺激物(STING)是负责RLR途径的重要衔接子,在哺乳动物的病毒RNA和DNA触发的IFN诱导中起着关键作用。为了了解STING在鱼类免疫系统中的作用,从草鱼(Ctenopharyngodon idella)中鉴定出STING基因(CiSTING)。 CiSTING的基因组序列为8548个碱基对(bp),包括899 bp的50个侧翼区域,7个外显子和6个内含子。预测启动子区域并验证启动子活性。 CiSTING cDNA为1358 bp,开放阅读框为1185 bp,编码394个氨基酸的多肽,在其N端区域带有信号肽和三个跨膜基序。 CiSTING的mRNA表达广泛分布在所研究的15个组织中,并且在体内外均被GCRV上调。同时,在体外受聚(I:C)或PGN刺激后,CiSTING的转录在早期被抑制,然后在后期被上调。有趣的是,CiSTING对体外脂多​​糖几乎没有影响。在CiSTING过表达的细胞中,GCRV或病毒/细菌PAMPs刺激后,CiTBK1,CiIRF3和CiIRF7显着上调。另外,在GCRV或PGN刺激后,CiIFN-1的转录被显着抑制,而CiMx1被上调。对于poly(I:C)刺激,CiIFN-1和CiMx1的mRNA表达在早期受到抑制,而在后期阶段则增强。 LPS刺激后,CiIFN-1和CiMx1均被抑制。此外,CiSTING的抗病毒活性通过抑制GCRV产量得到体现。综上所述,这些结果表明,CiSTING可能通过TBK1-IRF3 / IRF7级联参与板固有免疫应答,不仅以IFN依赖性途径响应dsRNA类似物,而且以IFN依赖性途径响应病毒和细菌PAMP。这项研究为STING在先天免疫中的重要作用提供了新颖的见解。

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