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dc.contributor.authorTeixeira, Rodrigo Antonio Parra [UNIFESP]
dc.contributor.authorMimura, Kallyne Kioko Oliveira [UNIFESP]
dc.contributor.authorAraujo, Leandro Pires [UNIFESP]
dc.contributor.authorGreco, Karin Vicente
dc.contributor.authorOliani, Sonia Maria [UNIFESP]
dc.date.accessioned2020-10-30T18:46:28Z
dc.date.available2020-10-30T18:46:28Z
dc.date.issued2016
dc.identifierhttps://doi.org/10.1002/term.1773
dc.identifier.citationJournal Of Tissue Engineering And Regenerative Medicine. Hoboken, v. 10, n. 2, p. E44-E53, 2016.
dc.identifier.issn1932-6254
dc.identifier.urihttps://repositorio.unifesp.br/handle/11600/58474
dc.description.abstractImmunosuppressive drugs have a critical role in inhibiting tissue damage and allograft rejection. Studies have demonstrated the anti-inflammatory effects of the annexin A1 (AnxA1) in the regulation of transmigration and apoptosis of leucocytes. In the present study, an experimental skin allograft model was used to evaluate a potential protective effect of AnxA1 in transplantation survival. Mice were used for the skin allograft model and pharmacological treatments were carried out using either the AnxA1 mimetic peptide Ac2-26, with or without cyclosporine A (CsA), starting 3days before surgery until rejection. Graft survival, skin histopathology, leucocyte transmigration and expression of AnxA1 and AnxA5 post-transplantation were analysed. Pharmacological treatment with Ac2-26 increased skin allograft survival related with inhibition of neutrophil transmigration and induction of apoptosis, thereby reducing the tissue damage compared with control animals. Moreover, AnxA1 and AnxA5 expression increased after Ac2-26 treatment in neutrophils. Interestingly, the combination of Ac2-26 and cyclosporine A showed similar survival of transplants when compared with the cyclosporine A group, which could be attributed to a synergistic effect of both drugs. Investigations in vitro revealed that cyclosporine A inhibited extracellular-signal-regulated kinase (ERK) phosphorylation induced by Ac2-26 in neutrophils. Overall, the results suggest that AnxA1 has an essential role in augmenting the survival of skin allograft, mainly owing to inhibition of neutrophil transmigration and enhancement of apoptosis. This effect may lead to the development of new therapeutic approaches relevant to transplant rejection. Copyright (c) 2013 John Wiley & Sons, Ltd.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Cientifico e Tecnologico - CNPq
dc.description.sponsorshipFundacao de Amparo a Pesquisa do Estado de Sao Paulo - FAPESP
dc.format.extentE44-E53
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofJournal Of Tissue Engineering And Regenerative Medicine
dc.rightsAcesso restrito
dc.subjectannexin A1en
dc.subjectcyclosporine Aen
dc.subjectneutrophilsen
dc.subjectskinen
dc.subjecttransplantationen
dc.titleThe essential role of annexin A1 mimetic peptide in the skin allograft survivalen
dc.typeArtigo
dc.description.affiliationFed Univ Sao Paulo UNIFESP, Postgrad Struct & Funct Biol, Sao Paulo, Brazil
dc.description.affiliationUCL, Northwick Pk Inst Med Res, Dept Surg Res, London, England
dc.description.affiliationSao Paulo State Univ UNESP, Inst Biociencias Letras & Ciencias Exatas IBILCE, Dept Biol, Sao Jose Do Rio Preto, Brazil
dc.description.affiliationUnifespFed Univ Sao Paulo UNIFESP, Postgrad Struct & Funct Biol, Sao Paulo, Brazil
dc.description.sponsorshipIDCNPq: 302768/2010-6
dc.description.sponsorshipIDCNPq: 132871/2007-6
dc.description.sponsorshipIDFAPESP: 2012/13041-4
dc.identifier.doi10.1002/term.1773
dc.description.sourceWeb of Science
dc.identifier.wosWOS:000370131300001
dc.coverageHoboken
dc.citation.volume10
dc.citation.issue2


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