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dc.contributor.advisorAspichueta Celaá, Patricia
dc.contributor.authorSyn, Wing-Kin
dc.date.accessioned2017-12-14T09:37:59Z
dc.date.available2017-12-14T09:37:59Z
dc.date.issued2017-09-19
dc.date.submitted2017-09-19
dc.identifier.urihttp://hdl.handle.net/10810/24048
dc.description150 p.es_ES
dc.description.abstractOsteopontin (OPN) is a cytokine and matrix molecule that is upregulated in human and mouse models of chronic liver injury and directly promotes liver fibrogenesis by activating hepatic stellate cells (HSC) and liver progenitors (LPC). OPN is secreted by multiple cell types including HSC, LPC, as well as recruited immune cells such as natural killer T (NKT) cells, which amplify the fibrogenic response. In vivo, OPN neutralization abrogates the LPC response, inhibits HSC activation, and reduces liver fibrosis, thus demonstrating that targeting OPN is a potentially attractive anti-fibrotic strategy.es_ES
dc.language.isoenges_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectgastroenterologyes_ES
dc.subjectgastroenterologíaes_ES
dc.titleThe role of osteopontin in liver fibrosises_ES
dc.typeinfo:eu-repo/semantics/doctoralThesises_ES
dc.rights.holder(c)2017 WING-KIN SYN
dc.identifier.studentID650526es_ES
dc.identifier.projectID14449es_ES
dc.departamentoesFisiologíaes_ES
dc.departamentoeuFisiologiaes_ES


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