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dc.contributor.authorChiricozzi, A.-
dc.contributor.authorRomanelli, M.-
dc.contributor.authorPanduri, S.-
dc.contributor.authorDonetti, E.-
dc.contributor.authorPrignano, F.-
dc.date.accessioned2022-03-01T13:04:23Z-
dc.date.available2022-03-01T13:04:23Z-
dc.date.issued2017-
dc.identifier.citationHistology and Histopathology, Vol.32, nº9, (2017)es
dc.identifier.issn1699-5848-
dc.identifier.issn0213-3911-
dc.identifier.urihttp://hdl.handle.net/10201/117514-
dc.description.abstractPsoriasis is a chronic skin disease characterized by the activation of various T cell subsets secreting IFNγ, IL-17, and IL-22, dendritic cells producing TNFα and IFNα, and other immune cells including neutrophils and mast cells. Keratinocytes respond to different cytokine signals orchestrating innate and adaptive immune responses. In vitro studies sought to clarify the cytokine effects on keratinocytes in order to evaluate the centrality of these mediators in psoriasis pathogenesis. The aim of this review is to highlight the relevance of this peculiar in vitro approach in investigating cytokine effects on skin or multilayered epidermis. Particularly, we reported keynfindinges
dc.formatapplication/pdfes
dc.format.extent6es
dc.languageenges
dc.publisherUniversidad de Murcia. Departamento de Biología Celular e Histologíaes
dc.relationSin financiación externa a la Universidades
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectPsoriasises
dc.subjectRHEes
dc.subjectSkin equivalentes
dc.subjectIL-17es
dc.subjectIL22es
dc.subjectTNFαes
dc.subjectIFNγes
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicina::616 - Patología. Medicina clínica. Oncologíaes
dc.titleRelevance of in vitro 3-D skin models in dissecting cytokine contribution to psoriasis pathogenesises
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.14670/HH-11-877-
Aparece en las colecciones:Vol.32, nº9 (2017)

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