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Modulation of calcium signaling pathway by hepatitis C virus core protein stimulates NLRP3 inflammasome activation

机译:丙型肝炎病毒核心蛋白对钙信号通路的调节可刺激NLRP3炎症小体活化

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摘要

Hepatitis C virus (HCV) infection remains a major cause of hepatic inflammation and liver disease. HCV triggers NLRP3 inflammasome activation and interleukin-1β (IL-1β) production from hepatic macrophages, or Kupffer cells, to drive the hepatic inflammatory response. Here we examined HCV activation of the NLRP3 inflammasome signaling cascade in primary human monocyte derived macrophages and THP-1 cell models of hepatic macrophages to define the HCV-specific agonist and cellular processes of inflammasome activation. We identified the HCV core protein as a virion-specific factor of inflammasome activation. The core protein was both necessary and sufficient for IL-1β production from macrophages exposed to HCV or soluble core protein alone. NLRP3 inflammasome activation by the HCV core protein required calcium mobilization linked with phospholipase-C activation. Our findings reveal a molecular basis of hepatic inflammasome activation and IL-1β release triggered by HCV core protein.
机译:丙型肝炎病毒(HCV)感染仍然是肝炎和肝病的主要原因。 HCV触发肝巨噬细胞或库普弗细胞产生NLRP3炎性体活化和白介素1β(IL-1β)产生,从而驱动肝炎性反应。在这里,我们检查了原代人单核细胞衍生的巨噬细胞和肝巨噬细胞的THP-1细胞模型中NLRP3炎性体信号传导级联的HCV激活,以定义HCV特异性激动剂和炎性体激活的细胞过程。我们将HCV核心蛋白鉴定为炎性体激活的病毒体特异性因子。对于从暴露于HCV的巨噬细胞或仅可溶性核心蛋白产生IL-1β而言,核心蛋白既必要又足够。 HCV核心蛋白对NLRP3炎性小体的激活需要钙动员和磷脂酶C激活。我们的发现揭示了由HCV核心蛋白触发的肝炎性小体活化和IL-1β释放的分子基础。

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