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dc.contributor.authorWight, TNen_US
dc.contributor.authorKang, Ien_US
dc.contributor.authorEvanko, SPen_US
dc.contributor.authorHarten, IAen_US
dc.contributor.authorChang, MYen_US
dc.contributor.authorPearce, OMTen_US
dc.contributor.authorAllen, CEen_US
dc.contributor.authorFrevert, CWen_US
dc.date.accessioned2020-09-17T08:44:30Z
dc.date.available2020-03-06en_US
dc.date.issued2020en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/67080
dc.description.abstractThe extracellular matrix (ECM) proteoglycan, versican increases along with other ECM versican binding molecules such as hyaluronan, tumor necrosis factor stimulated gene-6 (TSG-6), and inter alpha trypsin inhibitor (IαI) during inflammation in a number of different diseases such as cardiovascular and lung disease, autoimmune diseases, and several different cancers. These interactions form stable scaffolds which can act as "landing strips" for inflammatory cells as they invade tissue from the circulation. The increase in versican is often coincident with the invasion of leukocytes early in the inflammatory process. Versican interacts with inflammatory cells either indirectly via hyaluronan or directly via receptors such as CD44, P-selectin glycoprotein ligand-1 (PSGL-1), and toll-like receptors (TLRs) present on the surface of immune and non-immune cells. These interactions activate signaling pathways that promote the synthesis and secretion of inflammatory cytokines such as TNFα, IL-6, and NFκB. Versican also influences inflammation by interacting with a variety of growth factors and cytokines involved in regulating inflammation thereby influencing their bioavailability and bioactivity. Versican is produced by multiple cell types involved in the inflammatory process. Conditional total knockout of versican in a mouse model of lung inflammation demonstrated significant reduction in leukocyte invasion into the lung and reduced inflammatory cytokine expression. While versican produced by stromal cells tends to be pro-inflammatory, versican expressed by myeloid cells can create anti-inflammatory and immunosuppressive microenvironments. Inflammation in the tumor microenvironment often contains elevated levels of versican. Perturbing the accumulation of versican in tumors can inhibit inflammation and tumor progression in some cancers. Thus versican, as a component of the ECM impacts immunity and inflammation through regulating immune cell trafficking and activation. Versican is emerging as a potential target in the control of inflammation in a number of different diseases.en_US
dc.format.extent512 - ?en_US
dc.languageengen_US
dc.relation.ispartofFront Immunolen_US
dc.rightsThis is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectT lymphocytesen_US
dc.subjecthyaluronanen_US
dc.subjectimmunityen_US
dc.subjectinflammationen_US
dc.subjectmacrophagesen_US
dc.subjectversicanen_US
dc.titleVersican-A Critical Extracellular Matrix Regulator of Immunity and Inflammation.en_US
dc.typeArticle
dc.rights.holder© 2020 Wight, Kang, Evanko, Harten, Chang, Pearce, Allen and Frevert.
dc.identifier.doi10.3389/fimmu.2020.00512en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/32265939en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume11en_US
dcterms.dateAccepted2020-03-06en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Except where otherwise noted, this item's license is described as This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.