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dc.contributor.authorGopal, S
dc.contributor.authorArokiasamy, S
dc.contributor.authorPataki, C
dc.contributor.authorWhiteford, JR
dc.contributor.authorCouchman, JR
dc.date.accessioned2021-11-03T13:53:12Z
dc.date.available2021-11-03T13:53:12Z
dc.date.issued2021-02-10
dc.identifier.issn2046-2441
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/74993
dc.description.abstractThe syndecans are the major family of transmembrane proteoglycans, usually bearing multiple heparan sulfate chains. They are present on virtually all nucleated cells of vertebrates and are also present in invertebrates, indicative of a long evolutionary history. Genetic models in both vertebrates and invertebrates have shown that syndecans link to the actin cytoskeleton and can fine-tune cell adhesion, migration, junction formation, polarity and differentiation. Although often associated as co-receptors with other classes of receptors (e.g. integrins, growth factor and morphogen receptors), syndecans can nonetheless signal to the cytoplasm in discrete ways. Syndecan expression levels are upregulated in development, tissue repair and an array of human diseases, which has led to the increased appreciation that they may be important in pathogenesis not only as diagnostic or prognostic agents, but also as potential targets. Here, their functions in development and inflammatory diseases are summarized, including their potential roles as conduits for viral pathogen entry into cells.en_US
dc.format.extent200377
dc.languageeng
dc.publisherThe Royal Societyen_US
dc.relation.ispartofOpen Biology
dc.rightsPublished by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
dc.subjectcell adhesionen_US
dc.subjectglycosaminoglycanen_US
dc.subjectheparan sulfateen_US
dc.subjectinflammationen_US
dc.subjectproteoglycanen_US
dc.subjectstem cellen_US
dc.titleSyndecan receptors: pericellular regulators in development and inflammatory disease.en_US
dc.typeArticleen_US
dc.rights.holder© 2021 The Authors.
dc.identifier.doi10.1098/rsob.200377
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33561383en_US
pubs.issue2en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.publisher-urlhttps://doi.org/10.1098/rsob.200377
pubs.volume11en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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