Show simple item record

dc.contributor.authorMaler, MD
dc.contributor.authorNielsen, PJ
dc.contributor.authorStichling, N
dc.contributor.authorCohen, I
dc.contributor.authorRuzsics, Z
dc.contributor.authorWood, C
dc.contributor.authorEngelhard, P
dc.contributor.authorSuomalainen, M
dc.contributor.authorGyory, I
dc.contributor.authorHuber, M
dc.contributor.authorMüller-Quernheim, J
dc.contributor.authorSchamel, WWA
dc.contributor.authorGordon, S
dc.contributor.authorJakob, T
dc.contributor.authorMartin, SF
dc.contributor.authorJahnen-Dechent, W
dc.contributor.authorGreber, UF
dc.contributor.authorFreudenberg, MA
dc.contributor.authorFejer, Gyorgy
dc.date.accessioned2017-11-27T13:16:40Z
dc.date.available2017-11-27T13:16:40Z
dc.date.issued2017-09-06
dc.identifier.issn2161-2129
dc.identifier.issn2150-7511
dc.identifier.othere00670-17
dc.identifier.urihttp://hdl.handle.net/10026.1/10279
dc.description.abstract

<jats:title>ABSTRACT</jats:title> <jats:p>The scavenger receptor MARCO is expressed in several subsets of naive tissue-resident macrophages and has been shown to participate in the recognition of various bacterial pathogens. However, the role of MARCO in antiviral defense is largely unexplored. Here, we investigated whether MARCO might be involved in the innate sensing of infection with adenovirus and recombinant adenoviral vectors by macrophages, which elicit vigorous immune responses <jats:italic>in vivo</jats:italic>. Using cells derived from mice, we show that adenovirus infection is significantly more efficient in MARCO-positive alveolar macrophages (AMs) and in AM-like primary macrophage lines (Max Planck Institute cells) than in MARCO-negative bone marrow-derived macrophages. Using antibodies blocking ligand binding to MARCO, as well as gene-deficient and MARCO-transfected cells, we show that MARCO mediates the rapid adenovirus transduction of macrophages. By enhancing adenovirus infection, MARCO contributes to efficient innate virus recognition through the cytoplasmic DNA sensor cGAS. This leads to strong proinflammatory responses, including the production of interleukin-6 (IL-6), alpha/beta interferon, and mature IL-1α. These findings contribute to the understanding of viral pathogenesis in macrophages and may open new possibilities for the development of tools to influence the outcome of infection with adenovirus or adenovirus vectors. <jats:bold>IMPORTANCE</jats:bold> Macrophages play crucial roles in inflammation and defense against infection. Several macrophage subtypes have been identified with differing abilities to respond to infection with both natural adenoviruses and recombinant adenoviral vectors. Adenoviruses are important respiratory pathogens that elicit vigorous innate responses <jats:italic>in vitro</jats:italic> and <jats:italic>in vivo</jats:italic>. The cell surface receptors mediating macrophage type-specific adenovirus sensing are largely unknown. The scavenger receptor MARCO is expressed on some subsets of naive tissue-resident macrophages, including lung alveolar macrophages. Its role in antiviral macrophage responses is largely unexplored. Here, we studied whether the differential expression of MARCO might contribute to the various susceptibilities of macrophage subtypes to adenovirus. We demonstrate that MARCO significantly enhances adenovirus infection and innate responses in macrophages. These results help to understand adenoviral pathogenesis and may open new possibilities to influence the outcome of infection with adenoviruses or adenovirus vectors. <jats:bold>IMPORTANCE</jats:bold> Macrophages play crucial roles in inflammation and defense against infection. Several macrophage subtypes have been identified with differing abilities to respond to infection with both natural adenoviruses and recombinant adenoviral vectors. Adenoviruses are important respiratory pathogens that elicit vigorous innate responses <jats:italic>in vitro</jats:italic> and <jats:italic>in vivo</jats:italic>. The cell surface receptors mediating macrophage type-specific adenovirus sensing are largely unknown. The scavenger receptor MARCO is expressed on some subsets of naive tissue-resident macrophages, including lung alveolar macrophages. Its role in antiviral macrophage responses is largely unexplored. Here, we studied whether the differential expression of MARCO might contribute to the various susceptibilities of macrophage subtypes to adenovirus. We demonstrate that MARCO significantly enhances adenovirus infection and innate responses in macrophages. These results help to understand adenoviral pathogenesis and may open new possibilities to influence the outcome of infection with adenoviruses or adenovirus vectors.</jats:p>

dc.format.extent0-0
dc.format.mediumElectronic
dc.languageen
dc.language.isoen
dc.publisherAmerican Society for Microbiology
dc.subjectIL-1 alpha
dc.subjectMARCO
dc.subjectMPI cells
dc.subjectadenovirus
dc.subjectcGAS
dc.subjectcytokines
dc.subjectinnate immunity
dc.subjectmacrophages
dc.subjectscavenger receptor
dc.titleKey Role of the Scavenger Receptor MARCO in Mediating Adenovirus Infection and Subsequent Innate Responses of Macrophages
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000409384300056&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue4
plymouth.volume8
plymouth.publication-statusPublished
plymouth.journalmBio
dc.identifier.doi10.1128/mbio.00670-17
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/School of Biomedical Sciences
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CBR
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
plymouth.organisational-group/Plymouth/Users by role/Researchers in ResearchFish submission
dc.publisher.placeUnited States
dcterms.dateAccepted2017-05-31
dc.identifier.eissn2150-7511
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1128/mbio.00670-17
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2017-09-06
rioxxterms.typeJournal Article/Review
plymouth.funderEstablishment of non-transformed, continuously growing, alternatively activated mouse macrophage cell lines::NC3Rs


Files in this item

Thumbnail
Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record


All items in PEARL are protected by copyright law.
Author manuscripts deposited to comply with open access mandates are made available in accordance with publisher policies. Please cite only the published version using the details provided on the item record or document. In the absence of an open licence (e.g. Creative Commons), permissions for further reuse of content should be sought from the publisher or author.
Theme by 
Atmire NV