4.6 Review

Prevention of Cellular Suicide by Cytomegaloviruses

期刊

VIRUSES-BASEL
卷 4, 期 10, 页码 1928-1949

出版社

MDPI AG
DOI: 10.3390/v4101928

关键词

HCMV; UL36; UL37x1; UL38; m41.1; M45; m38.5; M36; beta 2.7; necroptosis

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资金

  1. Deutsche Forschungsgemeinschaft [BR1730/3-1]

向作者/读者索取更多资源

As intracellular parasites, viruses rely on many host cell functions to ensure their replication. The early induction of programmed cell death (PCD) in infected cells constitutes an effective antiviral host mechanism to restrict viral spread within an organism. As a countermeasure, viruses have evolved numerous strategies to interfere with the induction or execution of PCD. Slowly replicating viruses such as the cytomegaloviruses (CMVs) are particularly dependent on sustained cell viability. To preserve viability, the CMVs encode several viral cell death inhibitors that target different key regulators of the extrinsic and intrinsic apoptosis pathways. The best-characterized CMV-encoded inhibitors are the viral inhibitor of caspase-8-induced apoptosis (vICA), viral mitochondrial inhibitor of apoptosis (vMIA), and viral inhibitor of Bak oligomerization (vIBO). Moreover, a viral inhibitor of RIP-mediated signaling (vIRS) that blocks programmed necrosis has been identified in the genome of murine CMV (MCMV), indicating that this cell death mode is a particularly important part of the antiviral host response. This review provides an overview of the known cell death suppressors encoded by CMVs and their mechanisms of action.

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