Selected article for: "acid inducible gene and acute respiratory"

Author: Yang, Duo-Meng; Geng, Ting-Ting; Harrison, Andrew G.; Wang, Peng-Hua
Title: Differential roles of RIG-I like receptors in SARS-CoV-2 infection
  • Cord-id: 1wqrjuyq
  • Document date: 2021_9_7
  • ID: 1wqrjuyq
    Snippet: Retinoic acid-inducible gene I (RIG-I) and melanoma differentiation-associated protein 5 (MDA5) sense viral RNA and activate antiviral immune responses. Herein we investigate their functions in human epithelial cells, the primary and initial target of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). A deficiency in MDA5, RIG-I or mitochondrial antiviral signaling protein (MAVS) enhanced viral replication. The expression of the type I/III interferon (IFN) during infection was impaire
    Document: Retinoic acid-inducible gene I (RIG-I) and melanoma differentiation-associated protein 5 (MDA5) sense viral RNA and activate antiviral immune responses. Herein we investigate their functions in human epithelial cells, the primary and initial target of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). A deficiency in MDA5, RIG-I or mitochondrial antiviral signaling protein (MAVS) enhanced viral replication. The expression of the type I/III interferon (IFN) during infection was impaired in MDA5(−/−) and MAVS(−/−), but not in RIG-I(−/−), when compared to wild type (WT) cells. The mRNA level of full-length angiotensin-converting enzyme 2 (ACE2), the cellular entry receptor for SARS-CoV-2, was ~ 2.5-fold higher in RIG-I(−/−) than WT cells. These data demonstrate MDA5 as the predominant SARS-CoV-2 sensor, IFN-independent induction of ACE2 and anti-SARS-CoV-2 role of RIG-I in epithelial cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40779-021-00340-5.

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