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维生素D增强微小RNA - 130a对丙型肝炎病毒复制的抑制作用,且不依赖于I型干扰素信号通路。

Vitamin D Potentiates the Inhibitory Effect of MicroRNA-130a in Hepatitis C Virus Replication Independent of Type I Interferon Signaling Pathway.

作者信息

Duan Xiaoqiong, Guan Yujuan, Li Yujia, Chen Shan, Li Shilin, Chen Limin

机构信息

Institute of Blood Transfusion, Chinese Academy of Medical Sciences and Peking Union Medical College, Chengdu, China.

Guangzhou No. 8 People's Hospital, Guangzhou, China.

出版信息

Mediators Inflamm. 2015;2015:508989. doi: 10.1155/2015/508989. Epub 2015 Apr 28.

Abstract

Calcitriol, the bioactive metabolite of vitamin D, was reported to inhibit HCV production in a synergistic fashion with interferon, a treatment in vitro. Our previous study established that miR-130a inhibits HCV replication by restoring the host innate immune response. We aimed to determine whether there is additive inhibitory effect of calcitriol and miR-130a on HCV replication. Here we showed that calcitriol potentiates the anti-HCV effect of miR-130a in both Con1b replicon and J6/JFH1 culture systems. Intriguingly, this potentiating effect of calcitriol on miR-130a was not through upregulating the expression of cellular miR-130a or through increasing the miR-130a-mediated IFNα/β production. All these findings may contribute to the development of novel anti-HCV therapeutic strategies although the antiviral mechanism needs to be further investigated.

摘要

骨化三醇是维生素D的生物活性代谢产物,据报道,它在体外与干扰素协同抑制丙型肝炎病毒(HCV)的产生。我们之前的研究表明,miR-130a通过恢复宿主固有免疫反应来抑制HCV复制。我们旨在确定骨化三醇和miR-130a对HCV复制是否具有相加抑制作用。在此我们表明,在Con1b复制子和J6/JFH1培养系统中,骨化三醇均可增强miR-130a的抗HCV作用。有趣的是,骨化三醇对miR-130a的这种增强作用并非通过上调细胞miR-130a的表达或增加miR-130a介导的IFNα/β产生。尽管抗病毒机制有待进一步研究,但所有这些发现可能有助于开发新的抗HCV治疗策略。

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