タイトル |
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The RNA Sensor RIG-I Dually Functions as an Innate Sensor and Direct Antiviral Factor for Hepatitis B Virus
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その他のタイトル |
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RIG-I functions as a dual effector against HBV
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アクセス権 |
open access |
権利情報 |
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© 2015. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
- http://creativecommons.org/licenses/by-nc-nd/4.0/
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Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
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内容注記 |
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Supplemental materials are available on the publisher's website.
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Abstract
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Host innate recognition triggers key immune responses for viral elimination. The sensing mechanism of hepatitis B virus (HBV), a DNA virus, and the subsequent downstream signaling events remain to be fully clarified. Here we found that type III but not type I interferons are predominantly induced in human primary hepatocytes in response to HBV infection, through retinoic acid-inducible gene-I (RIG-I)-mediated sensing of the 5'-ε region of HBV pregenomic RNA. In addition, RIG-I could also counteract the interaction of HBV polymerase (P protein) with the 5'-ε region in an RNA-binding dependent manner, which consistently suppressed viral replication. Liposome-mediated delivery and vector-based expression of this ε region-derived RNA in liver abolished the HBV replication in human hepatocyte-chimeric mice. These findings identify an innate recognition mechanism by which RIG-I dually functions as an HBV sensor activating innate signaling and to counteract viral polymerase in human hepatocytes.
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出版者 |
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Cell Press
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資源タイプ |
journal article |
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AM |
資源識別子 |
HDL
http://hdl.handle.net/2115/62620
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関連 |
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DOI
https://doi.org/10.1016/j.immuni.2014.12.016
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PMID
25557055
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収録誌情報 |
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Immunity
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巻42
号1
開始ページ123
終了ページ132
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コンテンツ更新日時 |
2023-07-26 |