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Multiple Autonomous Cell Death Suppression Strategies Ensure Cytomegalovirus Fitness
Authors:Pratyusha Mandal  Lynsey N. Nagrani  Liliana Hernandez  Anita Louise McCormick  Christopher P. Dillon  Heather S. Koehler  Linda Roback  Emad S. Alnemri  Douglas R. Green  Edward S. Mocarski
Abstract:Programmed cell death pathways eliminate infected cells and regulate infection-associated inflammation during pathogen invasion. Cytomegaloviruses encode several distinct suppressors that block intrinsic apoptosis, extrinsic apoptosis, and necroptosis, pathways that impact pathogenesis of this ubiquitous herpesvirus. Here, we expanded the understanding of three cell autonomous suppression mechanisms on which murine cytomegalovirus relies: (i) M38.5-encoded viral mitochondrial inhibitor of apoptosis (vMIA), a BAX suppressor that functions in concert with M41.1-encoded viral inhibitor of BAK oligomerization (vIBO), (ii) M36-encoded viral inhibitor of caspase-8 activation (vICA), and (iii) M45-encoded viral inhibitor of RIP/RHIM activation (vIRA). Following infection of bone marrow-derived macrophages, the virus initially deflected receptor-interacting protein kinase (RIPK)3-dependent necroptosis, the most potent of the three cell death pathways. This process remained independent of caspase-8, although suppression of this apoptotic protease enhances necroptosis in most cell types. Second, the virus deflected TNF-mediated extrinsic apoptosis, a pathway dependent on autocrine TNF production by macrophages that proceeds independently of mitochondrial death machinery or RIPK3. Third, cytomegalovirus deflected BCL-2 family protein-dependent mitochondrial cell death through combined TNF-dependent and -independent signaling even in the absence of RIPK1, RIPK3, and caspase-8. Furthermore, each of these cell death pathways dictated a distinct pattern of cytokine and chemokine activation. Therefore, cytomegalovirus employs sequential, non-redundant suppression strategies to specifically modulate the timing and execution of necroptosis, extrinsic apoptosis, and intrinsic apoptosis within infected cells to orchestrate virus control and infection-dependent inflammation. Virus-encoded death suppressors together hold control over an intricate network that upends host defense and supports pathogenesis in the intact mammalian host.
Keywords:BCL2 family   mitochondria   serine protease   herpesvirus   apoptosis   extrinsic apoptosis   intrinsic apoptosis   pyroptosis   necroptosis   inflammation   TNF   IFN   DNA virus   cytomegalovirus   replication   HCMV   MCMV   cmvPCD   UL36   M36   vICA   M45   vIRA   M38.5   M41.1   vMIA   vIBO Caspase-8   RIPK1   RIPK3   myeloid cells   macrophages   cell death
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