Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in Vitro
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
dARK ID: | ark:/48912/001300000tf1x |
Texto Completo: | http://dx.doi.org/10.4049/jimmunol.1202030 http://repositorio.unifesp.br/handle/11600/36374 |
Resumo: | Annexin A1 (AnxAl) is a protein that displays potent anti-inflammatory properties, but its expression in eye tissue and its role in ocular inflammatory diseases have not been well studied. We investigated the mechanism of action and potential uses of AnxAl and its mimetic peptide (Ac2-26) in the endotoxin-induced uveitis (EIU) rodent model and in human ARPE-19 cells activated by LPS. in rats, analysis of untreated EIU after 24 and 48 h or EIU treated with topical applications or with a single s.c. injection of Ac2-26 revealed the anti-inflammatory actions of Ac2-26 on leukocyte infiltration and on the release of inflammatory mediators; the systemic administration of Boc2, a formylated peptide receptor (fpr) antagonist, abrogated the peptide's protective effects. Moreover, AnxA1(-/-) mice exhibited exacerbated EIU compared with wild-type animals Immunohistochemical studies of ocular tissue showed a specific AnxAl posttranslational modification in EIU and indicated that the fpr2 receptor mediated the anti-inflammatory actions of AnxAl. in vitro studies confirmed the roles of AnxAl and fpr2 and the protective effects of Ac2-26 on the release of chemical mediators in ARPE-19 cells. Molecular analysis of NF-kappa B translocation and IL-6, IL-8, and cyclooxygenase-2 gene expression indicated that the protective effects of AnxAl occur independently of the NF-kappa B signaling pathway and possibly in a posttranscriptional manner. Together, our data highlight the role of AnxAl in ocular inflammation, especially uveitis, and suggest the use of AnxAl or its mimetic peptide Ac2-26 as a therapeutic approach. |
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Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in VitroAnnexin A1 (AnxAl) is a protein that displays potent anti-inflammatory properties, but its expression in eye tissue and its role in ocular inflammatory diseases have not been well studied. We investigated the mechanism of action and potential uses of AnxAl and its mimetic peptide (Ac2-26) in the endotoxin-induced uveitis (EIU) rodent model and in human ARPE-19 cells activated by LPS. in rats, analysis of untreated EIU after 24 and 48 h or EIU treated with topical applications or with a single s.c. injection of Ac2-26 revealed the anti-inflammatory actions of Ac2-26 on leukocyte infiltration and on the release of inflammatory mediators; the systemic administration of Boc2, a formylated peptide receptor (fpr) antagonist, abrogated the peptide's protective effects. Moreover, AnxA1(-/-) mice exhibited exacerbated EIU compared with wild-type animals Immunohistochemical studies of ocular tissue showed a specific AnxAl posttranslational modification in EIU and indicated that the fpr2 receptor mediated the anti-inflammatory actions of AnxAl. in vitro studies confirmed the roles of AnxAl and fpr2 and the protective effects of Ac2-26 on the release of chemical mediators in ARPE-19 cells. Molecular analysis of NF-kappa B translocation and IL-6, IL-8, and cyclooxygenase-2 gene expression indicated that the protective effects of AnxAl occur independently of the NF-kappa B signaling pathway and possibly in a posttranscriptional manner. Together, our data highlight the role of AnxAl in ocular inflammation, especially uveitis, and suggest the use of AnxAl or its mimetic peptide Ac2-26 as a therapeutic approach.São Paulo State Univ, Inst Biociencias Letras & Ciencias Exatas, Dept Biol, BR-15054000 Sao Jose Do Rio Preto, BrazilIntegrated Coll Padre Albino Fdn, Dept Phys & Biol Sci, BR-15809144 Catanduva, SP, BrazilUniversidade Federal de São Paulo, Postgrad Struct & Funct Biol, BR-04023900 São Paulo, BrazilUniv São Paulo, Dept Clin & Toxicol Anal, BR-05508900 São Paulo, BrazilQueen Mary Univ London, Barts & London Sch Med & Dent, William Harvey Res Inst, London EC1M 6BQ, EnglandUniversidade Federal de São Paulo, Dept Morphol & Genet, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Postgrad Struct & Funct Biol, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morphol & Genet, BR-04023900 São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)FAPESP: 2011/00128-1FAPESP: 2009/15240-1CNPq: 472056/2009-3CNPq: 301677/2011-5Amer Assoc ImmunologistsSão Paulo State UnivIntegrated Coll Padre Albino FdnUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Queen Mary Univ LondonGirol, Ana Paula [UNIFESP]Mimura, Kallyne Kioko Oliveira [UNIFESP]Drewes, Carine CristianeBoonheis, Simone M.Solito, EgleFarsky, Sandra Helena PoliselliGil, Cristiane Damas [UNIFESP]Oliani, Sonia Maria [UNIFESP]2016-01-24T14:31:49Z2016-01-24T14:31:49Z2013-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion5689-5701http://dx.doi.org/10.4049/jimmunol.1202030Journal of Immunology. Bethesda: Amer Assoc Immunologists, v. 190, n. 11, p. 5689-5701, 2013.10.4049/jimmunol.12020300022-1767http://repositorio.unifesp.br/handle/11600/36374WOS:000319205900039ark:/48912/001300000tf1xengJournal of Immunologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T12:31:49Zoai:repositorio.unifesp.br/:11600/36374Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:37:19.484400Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in Vitro |
title |
Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in Vitro |
spellingShingle |
Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in Vitro Girol, Ana Paula [UNIFESP] |
title_short |
Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in Vitro |
title_full |
Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in Vitro |
title_fullStr |
Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in Vitro |
title_full_unstemmed |
Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in Vitro |
title_sort |
Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in Vitro |
author |
Girol, Ana Paula [UNIFESP] |
author_facet |
Girol, Ana Paula [UNIFESP] Mimura, Kallyne Kioko Oliveira [UNIFESP] Drewes, Carine Cristiane Boonheis, Simone M. Solito, Egle Farsky, Sandra Helena Poliselli Gil, Cristiane Damas [UNIFESP] Oliani, Sonia Maria [UNIFESP] |
author_role |
author |
author2 |
Mimura, Kallyne Kioko Oliveira [UNIFESP] Drewes, Carine Cristiane Boonheis, Simone M. Solito, Egle Farsky, Sandra Helena Poliselli Gil, Cristiane Damas [UNIFESP] Oliani, Sonia Maria [UNIFESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
São Paulo State Univ Integrated Coll Padre Albino Fdn Universidade Federal de São Paulo (UNIFESP) Universidade de São Paulo (USP) Queen Mary Univ London |
dc.contributor.author.fl_str_mv |
Girol, Ana Paula [UNIFESP] Mimura, Kallyne Kioko Oliveira [UNIFESP] Drewes, Carine Cristiane Boonheis, Simone M. Solito, Egle Farsky, Sandra Helena Poliselli Gil, Cristiane Damas [UNIFESP] Oliani, Sonia Maria [UNIFESP] |
description |
Annexin A1 (AnxAl) is a protein that displays potent anti-inflammatory properties, but its expression in eye tissue and its role in ocular inflammatory diseases have not been well studied. We investigated the mechanism of action and potential uses of AnxAl and its mimetic peptide (Ac2-26) in the endotoxin-induced uveitis (EIU) rodent model and in human ARPE-19 cells activated by LPS. in rats, analysis of untreated EIU after 24 and 48 h or EIU treated with topical applications or with a single s.c. injection of Ac2-26 revealed the anti-inflammatory actions of Ac2-26 on leukocyte infiltration and on the release of inflammatory mediators; the systemic administration of Boc2, a formylated peptide receptor (fpr) antagonist, abrogated the peptide's protective effects. Moreover, AnxA1(-/-) mice exhibited exacerbated EIU compared with wild-type animals Immunohistochemical studies of ocular tissue showed a specific AnxAl posttranslational modification in EIU and indicated that the fpr2 receptor mediated the anti-inflammatory actions of AnxAl. in vitro studies confirmed the roles of AnxAl and fpr2 and the protective effects of Ac2-26 on the release of chemical mediators in ARPE-19 cells. Molecular analysis of NF-kappa B translocation and IL-6, IL-8, and cyclooxygenase-2 gene expression indicated that the protective effects of AnxAl occur independently of the NF-kappa B signaling pathway and possibly in a posttranscriptional manner. Together, our data highlight the role of AnxAl in ocular inflammation, especially uveitis, and suggest the use of AnxAl or its mimetic peptide Ac2-26 as a therapeutic approach. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-06-01 2016-01-24T14:31:49Z 2016-01-24T14:31:49Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.4049/jimmunol.1202030 Journal of Immunology. Bethesda: Amer Assoc Immunologists, v. 190, n. 11, p. 5689-5701, 2013. 10.4049/jimmunol.1202030 0022-1767 http://repositorio.unifesp.br/handle/11600/36374 WOS:000319205900039 |
dc.identifier.dark.fl_str_mv |
ark:/48912/001300000tf1x |
url |
http://dx.doi.org/10.4049/jimmunol.1202030 http://repositorio.unifesp.br/handle/11600/36374 |
identifier_str_mv |
Journal of Immunology. Bethesda: Amer Assoc Immunologists, v. 190, n. 11, p. 5689-5701, 2013. 10.4049/jimmunol.1202030 0022-1767 WOS:000319205900039 ark:/48912/001300000tf1x |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Immunology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
5689-5701 |
dc.publisher.none.fl_str_mv |
Amer Assoc Immunologists |
publisher.none.fl_str_mv |
Amer Assoc Immunologists |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1818602517110456320 |