Key Role of the Scavenger Receptor MARCO in Mediating Adenovirus Infection and Subsequent Innate Responses of Macrophages
dc.contributor.author | Maler, MD | |
dc.contributor.author | Nielsen, PJ | |
dc.contributor.author | Stichling, N | |
dc.contributor.author | Cohen, I | |
dc.contributor.author | Ruzsics, Z | |
dc.contributor.author | Wood, C | |
dc.contributor.author | Engelhard, P | |
dc.contributor.author | Suomalainen, M | |
dc.contributor.author | Gyory, I | |
dc.contributor.author | Huber, M | |
dc.contributor.author | Müller-Quernheim, J | |
dc.contributor.author | Schamel, WWA | |
dc.contributor.author | Gordon, S | |
dc.contributor.author | Jakob, T | |
dc.contributor.author | Martin, SF | |
dc.contributor.author | Jahnen-Dechent, W | |
dc.contributor.author | Greber, UF | |
dc.contributor.author | Freudenberg, MA | |
dc.contributor.author | Fejer, Gyorgy | |
dc.date.accessioned | 2017-11-27T13:16:40Z | |
dc.date.available | 2017-11-27T13:16:40Z | |
dc.date.issued | 2017-09-06 | |
dc.identifier.issn | 2161-2129 | |
dc.identifier.issn | 2150-7511 | |
dc.identifier.other | e00670-17 | |
dc.identifier.uri | http://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.extent | 0-0 | |
dc.format.medium | Electronic | |
dc.language | en | |
dc.language.iso | en | |
dc.publisher | American Society for Microbiology | |
dc.subject | IL-1 alpha | |
dc.subject | MARCO | |
dc.subject | MPI cells | |
dc.subject | adenovirus | |
dc.subject | cGAS | |
dc.subject | cytokines | |
dc.subject | innate immunity | |
dc.subject | macrophages | |
dc.subject | scavenger receptor | |
dc.title | Key Role of the Scavenger Receptor MARCO in Mediating Adenovirus Infection and Subsequent Innate Responses of Macrophages | |
dc.type | journal-article | |
dc.type | Journal Article | |
dc.type | Research Support, Non-U.S. Gov't | |
plymouth.author-url | https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000409384300056&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008 | |
plymouth.issue | 4 | |
plymouth.volume | 8 | |
plymouth.publication-status | Published | |
plymouth.journal | mBio | |
dc.identifier.doi | 10.1128/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.place | United States | |
dcterms.dateAccepted | 2017-05-31 | |
dc.identifier.eissn | 2150-7511 | |
dc.rights.embargoperiod | Not known | |
rioxxterms.versionofrecord | 10.1128/mbio.00670-17 | |
rioxxterms.licenseref.uri | http://www.rioxx.net/licenses/all-rights-reserved | |
rioxxterms.licenseref.startdate | 2017-09-06 | |
rioxxterms.type | Journal Article/Review | |
plymouth.funder | Establishment of non-transformed, continuously growing, alternatively activated mouse macrophage cell lines::NC3Rs |