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细胞因子样迷走神经通过IKK-NF-κB信号通路介导的抗病毒反应。 (注:原文中“in via”表述有误,推测可能是“in vivo”即“在体内”的意思,基于此给出上述译文)

Cytokine-like-Vago-mediated antiviral response in via IKK-NF-κB signaling pathway.

作者信息

Nanakorn Zittipong, Kawai Taro, Tassanakajon Anchalee

机构信息

Center of Excellence for Molecular Biology and Genomics of Shrimp, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.

Laboratory of Molecular Immunobiology, Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology, Nara 630-0192, Japan.

出版信息

iScience. 2024 May 31;27(7):110161. doi: 10.1016/j.isci.2024.110161. eCollection 2024 Jul 19.

Abstract

Interferon (IFN) system is the primary mechanism of innate antiviral defense in immune response. To date, limited studies of IFN system were conducted in crustaceans. Previous report in demonstrated the interconnection of cytokine-like molecule Vago and inhibitor of kappa B kinase-nuclear factor κB (IKK-NF-κB) cascade against white spot syndrome virus (WSSV). This study further identified five different isoforms. Upon immune stimulation, expressed against shrimp pathogens. , and highly responded to WSSV, whereas, and RNAi exhibited a rapid mortality with elevated WSSV replication. Suppression of and negatively affected proPO system, genes in signal transduction, and AMPs. WSSV infection additionally induced Vaog4 granule accumulation and cellular translocation to the area of cell membrane. More importantly, and promoters were stimulated by IKK overexpression; meanwhile, they further activated and promoter activities. These results suggested the possible roles of the cytokine-like via IKK-NF-κB cascade against WSSV infection.

摘要

干扰素(IFN)系统是免疫应答中先天性抗病毒防御的主要机制。迄今为止,在甲壳类动物中对IFN系统的研究有限。之前的报告表明细胞因子样分子Vago与κB激酶-核因子κB(IKK-NF-κB)级联反应针对白斑综合征病毒(WSSV)存在相互联系。本研究进一步鉴定出五种不同的亚型。在免疫刺激下,其表达针对虾类病原体。其中,[具体亚型1]、[具体亚型2]和[具体亚型3]对WSSV反应强烈,而[具体亚型4]和[具体亚型5]的RNA干扰导致对虾在WSSV复制增加的情况下迅速死亡。对[具体亚型4]和[具体亚型5]的抑制对酚氧化酶原系统、信号转导中的基因以及抗菌肽产生负面影响。WSSV感染还诱导了Vaog4颗粒的积累以及细胞向细胞膜区域的转运。更重要的是,[具体亚型1]和[具体亚型2]的启动子受到IKK过表达的刺激;同时,它们进一步激活了[具体亚型3]和[具体亚型4]的启动子活性。这些结果表明细胞因子样[具体分子]可能通过IKK-NF-κB级联反应在抵抗WSSV感染中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b652/11226982/b0fe97e182da/fx1.jpg

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