Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation in Vivo and in Vitro

Detalhes bibliográficos
Autor(a) principal: Girol, Ana Paula [UNIFESP]
Data de Publicação: 2013
Outros Autores: 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]
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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spelling 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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