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

机译:维生素D有效地增强了MicroRNA-130a在丙型肝炎病毒复制中的抑制作用,无论如何I型干扰素信号通路

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摘要

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.
机译:据报道,求解维生素D的生物活性代谢物,以抑制干扰素的协同时尚,体外治疗抑制HCV产量。我们以前的研究确定MIR-130A通过恢复主体先天免疫应答来抑制HCV复制。我们的目标是判断钙聚合物和miR-130a对HCV复制是否存在添加剂抑制作用。在这里,我们表明,CalcIr醇增强了MiR-130a在Con1B Replicon和J6 / JFH1培养系统中的抗HCV效应。有趣的是,CalciTiol对miR-130a上的这种增性作用不是通过上调细胞miR-130a的表达或通过增加miR-130a介导的IFNα/β的产生。尽管需要进一步调查抗病毒机制,但所有这些调查结果可能导致新型抗HCV治疗策略的发展。

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