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鲤疱疹病毒2型miR-C12通过靶向作用减弱病毒介导的细胞凋亡并促进病毒增殖

Cyprinid Herpesvirus 2 miR-C12 Attenuates Virus-Mediated Apoptosis and Promotes Virus Propagation by Targeting .

作者信息

Lu Jianfei, Shen Zhaoyuan, Lu Liqun, Xu Dan

机构信息

State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-Products, Ningbo University, Ningbo, China.

Laboratory of Biochemistry and Molecular Biology, School of Marine Sciences, Ningbo University, Ningbo, China.

出版信息

Front Microbiol. 2019 Dec 18;10:2923. doi: 10.3389/fmicb.2019.02923. eCollection 2019.

DOI:10.3389/fmicb.2019.02923
PMID:31921084
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6930231/
Abstract

DNA viruses, most notably members of the herpesvirus family, generally encode miRNAs to mediate both virus and host genes expression. We previously demonstrated that Cyprinid herpesvirus 2 (CyHV-2) encodes 17 miRNAs that are involved in innate immune signaling pathways. In this study, the function of CyHV-2-encoded miRNA was further investigated in GiCF cells. We found that miR-C4 promoted CyHV-2-induced apoptosis, while miR-C12 decreased CyHV-2-induced apoptosis. miR-C12 targeted to 3' UTR sequence of and suppressed the expression of . Besides, the silencing of caspase 8 by specific siRNA led to the attenuation of CyHV-2-induced apoptosis. Furthermore, caspase 8 was downregulated in cells transfected with miR-C12 during CyHV-2 infection. Overexpression of miR-C12 significantly suppressed CyHV-2-induced apoptosis, while silencing of miR-C12 promoted CyHV-2-induced apoptosis. Finally, inhibition of miR-C12 resulted in suppression of CyHV-2 propagation, overexpression of miR-C12, and CASP8-siRNA-1 facilitated CyHV-2 propagation. Taken together, our results demonstrated that CyHV-2-encoded miR-C12 to suppress virus-induced apoptosis and promoted virus replication by targeting .

摘要

DNA病毒,最显著的是疱疹病毒科的成员,通常编码微小RNA(miRNA)来介导病毒和宿主基因的表达。我们之前证明鲤疱疹病毒2型(CyHV-2)编码17种参与先天免疫信号通路的miRNA。在本研究中,我们在GiCF细胞中进一步研究了CyHV-2编码的miRNA的功能。我们发现miR-C4促进CyHV-2诱导的细胞凋亡,而miR-C12减少CyHV-2诱导的细胞凋亡。miR-C12靶向……的3'非翻译区(UTR)序列并抑制……的表达。此外,用特异性小干扰RNA(siRNA)沉默半胱天冬酶8导致CyHV-2诱导的细胞凋亡减弱。此外,在CyHV-2感染期间,用miR-C12转染的细胞中半胱天冬酶8表达下调。miR-C12的过表达显著抑制CyHV-2诱导的细胞凋亡,而miR-C12的沉默促进CyHV-2诱导的细胞凋亡。最后,抑制miR-C12导致CyHV-2增殖受到抑制,miR-C12的过表达以及CASP8-siRNA-1促进CyHV-2增殖。综上所述,我们的结果表明,CyHV-2编码的miR-C12通过靶向……来抑制病毒诱导的细胞凋亡并促进病毒复制。 (注:原文中部分内容缺失,用“……”表示)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/87a6f056a002/fmicb-10-02923-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/2b11d42006b1/fmicb-10-02923-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/a0358f36c676/fmicb-10-02923-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/0e5543f20639/fmicb-10-02923-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/5b7a21a0afe8/fmicb-10-02923-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/d0c5975caf2e/fmicb-10-02923-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/9dc072e18c04/fmicb-10-02923-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/87a6f056a002/fmicb-10-02923-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/2b11d42006b1/fmicb-10-02923-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/a0358f36c676/fmicb-10-02923-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/0e5543f20639/fmicb-10-02923-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/5b7a21a0afe8/fmicb-10-02923-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/d0c5975caf2e/fmicb-10-02923-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/9dc072e18c04/fmicb-10-02923-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e76/6930231/87a6f056a002/fmicb-10-02923-g007.jpg

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Bone marrow-derived mesenchymal stem cells-derived exosomes prevent oligodendrocyte apoptosis through exosomal miR-134 by targeting caspase-8.骨髓间充质干细胞来源的外泌体通过靶向半胱天冬酶-8,经由外泌体miR-134预防少突胶质细胞凋亡。
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