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dc.contributor.authorHolm, Christian K.
dc.contributor.authorJensen, Soren B.
dc.contributor.authorJakobsen, Martin R.
dc.contributor.authorCheshenko, Natalia
dc.contributor.authorHoran, Kristy A.
dc.contributor.authorMoeller, Hanne B.
dc.contributor.authorGonzalez-Dosal, Regina
dc.contributor.authorRasmussen, Simon B.
dc.contributor.authorChristensen, Maria H.
dc.contributor.authorYarovinsky, Timur O.
dc.contributor.authorRixon, Frazer J.
dc.contributor.authorHerold, Betsy C.
dc.contributor.authorFitzgerald, Katherine A.
dc.contributor.authorPaludan, Soren R.
dc.date2022-08-11T08:09:08.000
dc.date.accessioned2022-08-23T16:18:54Z
dc.date.available2022-08-23T16:18:54Z
dc.date.issued2012-06-17
dc.date.submitted2013-01-31
dc.identifier.citationNat Immunol. 2012 Jun 17;13(8):737-43. doi: 10.1038/ni.2350. <a href="http://dx.doi.org/10.1038/ni.2350" target="_blank">Link to article on publisher's site</a>
dc.identifier.issn1529-2908 (Linking)
dc.identifier.doi10.1038/ni.2350
dc.identifier.pmid22706339
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34920
dc.description.abstractThe innate immune system senses infection by detecting either evolutionarily conserved molecules essential for the survival of microbes or the abnormal location of molecules. Here we demonstrate the existence of a previously unknown innate detection mechanism induced by fusion between viral envelopes and target cells. Virus-cell fusion specifically stimulated a type I interferon response with expression of interferon-stimulated genes, in vivo recruitment of leukocytes and potentiation of signaling via Toll-like receptor 7 (TLR7) and TLR9. The fusion-dependent response was dependent on the stimulator of interferon genes STING but was independent of DNA, RNA and viral capsid. We suggest that membrane fusion is sensed as a danger signal with potential implications for defense against enveloped viruses and various conditions of giant-cell formation.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=22706339&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3411909/pdf/nihms379462.pdf
dc.subjectAnimals
dc.subject*Cell Fusion
dc.subjectChemokine CXCL10
dc.subjectHEK293 Cells
dc.subjectHeLa Cells
dc.subjectHerpesvirus 1, Human
dc.subjectHumans
dc.subject*Immunity, Innate
dc.subjectInterferon Type I
dc.subjectLeukocytes
dc.subjectLymphocyte Activation
dc.subjectMacrophages
dc.subject*Membrane Fusion
dc.subjectMembrane Glycoproteins
dc.subjectMembrane Proteins
dc.subjectMice
dc.subjectMice, Knockout
dc.subjectMyeloid Differentiation Factor 88
dc.subjectSignal Transduction
dc.subjectToll-Like Receptor 7
dc.subjectToll-Like Receptor 9
dc.subjectVirus Internalization
dc.subjectImmunology and Infectious Disease
dc.titleVirus-cell fusion as a trigger of innate immunity dependent on the adaptor STING
dc.typeJournal Article
dc.source.journaltitleNature immunology
dc.source.volume13
dc.source.issue8
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/infdis_pp/145
dc.identifier.contextkey3631085
html.description.abstract<p>The innate immune system senses infection by detecting either evolutionarily conserved molecules essential for the survival of microbes or the abnormal location of molecules. Here we demonstrate the existence of a previously unknown innate detection mechanism induced by fusion between viral envelopes and target cells. Virus-cell fusion specifically stimulated a type I interferon response with expression of interferon-stimulated genes, in vivo recruitment of leukocytes and potentiation of signaling via Toll-like receptor 7 (TLR7) and TLR9. The fusion-dependent response was dependent on the stimulator of interferon genes STING but was independent of DNA, RNA and viral capsid. We suggest that membrane fusion is sensed as a danger signal with potential implications for defense against enveloped viruses and various conditions of giant-cell formation.</p>
dc.identifier.submissionpathinfdis_pp/145
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology
dc.source.pages737-43


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