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首页> 外文期刊>Journal of Turbulence >Mutual Regulation of NOD2 and RIG-I in Zebrafish Provides Insights into the Coordination between Innate Antibacterial and Antiviral Signaling Pathways
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Mutual Regulation of NOD2 and RIG-I in Zebrafish Provides Insights into the Coordination between Innate Antibacterial and Antiviral Signaling Pathways

机译:斑马鱼中的NOD2和RIG-I的相互调节提供了先天抗菌和抗病毒信号通路之间的协调的见解

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摘要

Nucleotide-binding oligomerization domain-containing protein 2 (NOD2) and retinoic acid-inducible gene I (RIG-I) are two important cytosolic pattern recognition receptors (PRRs) in the recognition of pathogen-associated molecular patterns (PAMPs), initiating innate antibacterial and antiviral signaling pathways. However, the relationship between these PRRs, especially in teleost fish models, is rarely reported. In this article, we describe the mutual regulation of zebrafish NOD2 (DrNOD2) and RIG-I (DrRIG-I) in innate immune responses. Luciferase assays were conducted to determine the activation of NF-B and interferon signaling. Morpholino-mediated knockdown and mRNA-mediated rescue were performed to further confirm the regulatory roles between DrNOD2 and DrRIG-I. Results showed that DrNOD2 and DrRIG-I shared conserved structural hallmarks with their mammalian counterparts, and activated DrRIG-I signaling can induce DrNOD2 production. Surprisingly, DrNOD2-initiated signaling can also induce DrRIG-I expression, indicating that a mutual regulatory mechanism may exist between them. Studies conducted using HEK293T cells and zebrafish embryos showed that DrRIG-I could negatively regulate DrNOD2-activated NF-B signaling, and DrNOD2 could inhibit DrRIG-I-induced IFN signaling. Moreover, knocking down DrRIG-I expression by morpholino could enhance DrNOD2-initiated NF-B activation, and vice versa, which could be rescued by their corresponding mRNAs. Results revealed a mutual feedback regulatory mechanism underlying NOD2 and RIG-I signaling pathways in teleosts. This mechanism reflects the coordination between cytosolic antibacterial and antiviral PRRs in the complex network of innate immunity.
机译:含有核苷酸结合的寡聚化结构域蛋白2(NOD2)和视黄酸 - 诱导基因I(RIG-I)是识别病原体相关分子模式(PAMPS)的两个重要细胞源图案识别受体(PRR),启动先天抗菌剂和抗病毒信号传导途径。然而,很少报道这些PRR之间的关系,特别是在远程鱼类模型中。在本文中,我们描述了斑马鱼NOD2(DRNOD2)和钻石I(DRRIG-I)的相互调节。进行荧光素酶测定以确定NF-B和干扰素信号传导的活化。进行吗啉介导的敲低和mRNA介导的救援,以进一步证实DRNOD2和DRRIG-I之间的调节作用。结果表明,DRNOD2和DRRIG-I与其哺乳动物对应物共享保守的结构标志,并激活DRRIG-I信令可以诱导DRNOD2生产。令人惊讶的是,DRNOD2引发的信令还可以诱导DRRIG-I表达,表明它们之间可能存在相互监管机制。使用HEK293T细胞和斑马鱼胚进行的研究表明,DRRIG-I可以负调节DRNOD2激活的NF-B信令,并且DRNOD2可以抑制DRRIG-I诱导的IFN信号传导。此外,通过吗啉代敲击DRRIG-I表达可以增强DRNOD2引发的NF-B激活,反之亦然,其可以通过它们对应的MRNA来救出。结果显示了Nod2和Roidss中的互联网上的相互反馈监管机制。该机制反映了在先天免疫网络复杂网络中的细胞溶化抗菌和抗病毒PRR之间的协调。

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