The involvement of anti-inflammatory protein, Annexin A1, in ocular toxoplasmosis
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://www.molvis.org/molvis/v18/a163/ http://repositorio.unifesp.br/handle/11600/44936 |
Resumo: | Purpose: The aim of this study was to evaluate the expression of the protein annexin A1 (ANXA1), a potent endogenous regulator of the inflammatory process, in ocular toxoplasmosis.Methods: C57BL/ 6 female mice were infected using intravitreal injections of either 10(6) tachyzoites of Toxoplasma gondii (RH strain; T. gondii) or PBS only (control groups). After 24, 48, and 72 h, animals were sacrificed and their eyes were harvested for histopathological, immunohistochemical, and ultrastructural immunocytochemical analysis of ANXA1. Human retinal pigment epithelial (RPE) cells (ARPE-19) were infected in vitro with T. gondii and collected after 60, 120, 240 min, and 24 h.Results: Compared with non-infected eyes, an intense inflammatory response was observed in the anterior (24 h after infection) and posterior segments (72 h after infection) of the infected eye, characterized by neutrophil infiltration and by the presence of tachyzoites and their consequent destruction along with disorganization of normal retina architecture and RPE vacuolization. T. gondii infection was associated with a significant increase of ANXA1 expression in the neutrophils at 24, 48, and 72 h, and in the RPE at 48 and 72 h. In vitro studies confirmed an upregulation of ANXA1 levels in RPE cells, after 60 and 120 min of infection with T. gondii.Conclusions: The positive modulation of endogenous ANXA1 in the inflammatory and RPE cells during T. gondii infection suggests that this protein may serve as a therapeutic target in ocular toxoplasmosis. |
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The involvement of anti-inflammatory protein, Annexin A1, in ocular toxoplasmosisPurpose: The aim of this study was to evaluate the expression of the protein annexin A1 (ANXA1), a potent endogenous regulator of the inflammatory process, in ocular toxoplasmosis.Methods: C57BL/ 6 female mice were infected using intravitreal injections of either 10(6) tachyzoites of Toxoplasma gondii (RH strain; T. gondii) or PBS only (control groups). After 24, 48, and 72 h, animals were sacrificed and their eyes were harvested for histopathological, immunohistochemical, and ultrastructural immunocytochemical analysis of ANXA1. Human retinal pigment epithelial (RPE) cells (ARPE-19) were infected in vitro with T. gondii and collected after 60, 120, 240 min, and 24 h.Results: Compared with non-infected eyes, an intense inflammatory response was observed in the anterior (24 h after infection) and posterior segments (72 h after infection) of the infected eye, characterized by neutrophil infiltration and by the presence of tachyzoites and their consequent destruction along with disorganization of normal retina architecture and RPE vacuolization. T. gondii infection was associated with a significant increase of ANXA1 expression in the neutrophils at 24, 48, and 72 h, and in the RPE at 48 and 72 h. In vitro studies confirmed an upregulation of ANXA1 levels in RPE cells, after 60 and 120 min of infection with T. gondii.Conclusions: The positive modulation of endogenous ANXA1 in the inflammatory and RPE cells during T. gondii infection suggests that this protein may serve as a therapeutic target in ocular toxoplasmosis.Fed Univ Sao Paulo UNIFESP, Dept Morphol & Genet, Sao Paulo, BrazilInst Oswaldo Cruz FIOCRUZ, Lab Imunomodulacao & Protozool, Rio De Janeiro, RJ, BrazilSao Paulo State Univ UNESP, Inst Biociencias Letras & Ciencias Exatas IBILCE, Dept Biol, Sao Jose Do Rio Preto, SP, BrazilFed Univ Sao Paulo UNIFESP, Dept Morphol & Genet, Sao Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)FAPESP: 2011/00128-1FAPESP: 2009/15240-1CNPq: 302768/2010-6Molecular VisionUniversidade Federal de São Paulo (UNIFESP)Inst Oswaldo Cruz FIOCRUZSao Paulo State Univ UNESPMimura, Kallyne Kioko OliveiraTedesco, Roberto Carlos [UNIFESP]Calabrese, Katia da SilvaGil, Cristiane Damas [UNIFESP]Oliani, Sonia Maria2018-06-18T11:04:11Z2018-06-18T11:04:11Z2012-06-15info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1583-1593http://www.molvis.org/molvis/v18/a163/Molecular Vision. Atlanta: Molecular Vision, v. 18, n. 163-64, p. 1583-1593, 2012.1090-0535http://repositorio.unifesp.br/handle/11600/44936WOS:000305554600001engMolecular Visioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-05-02T15:51:51Zoai:repositorio.unifesp.br/:11600/44936Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-05-02T15:51:51Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
The involvement of anti-inflammatory protein, Annexin A1, in ocular toxoplasmosis |
title |
The involvement of anti-inflammatory protein, Annexin A1, in ocular toxoplasmosis |
spellingShingle |
The involvement of anti-inflammatory protein, Annexin A1, in ocular toxoplasmosis Mimura, Kallyne Kioko Oliveira |
title_short |
The involvement of anti-inflammatory protein, Annexin A1, in ocular toxoplasmosis |
title_full |
The involvement of anti-inflammatory protein, Annexin A1, in ocular toxoplasmosis |
title_fullStr |
The involvement of anti-inflammatory protein, Annexin A1, in ocular toxoplasmosis |
title_full_unstemmed |
The involvement of anti-inflammatory protein, Annexin A1, in ocular toxoplasmosis |
title_sort |
The involvement of anti-inflammatory protein, Annexin A1, in ocular toxoplasmosis |
author |
Mimura, Kallyne Kioko Oliveira |
author_facet |
Mimura, Kallyne Kioko Oliveira Tedesco, Roberto Carlos [UNIFESP] Calabrese, Katia da Silva Gil, Cristiane Damas [UNIFESP] Oliani, Sonia Maria |
author_role |
author |
author2 |
Tedesco, Roberto Carlos [UNIFESP] Calabrese, Katia da Silva Gil, Cristiane Damas [UNIFESP] Oliani, Sonia Maria |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Inst Oswaldo Cruz FIOCRUZ Sao Paulo State Univ UNESP |
dc.contributor.author.fl_str_mv |
Mimura, Kallyne Kioko Oliveira Tedesco, Roberto Carlos [UNIFESP] Calabrese, Katia da Silva Gil, Cristiane Damas [UNIFESP] Oliani, Sonia Maria |
description |
Purpose: The aim of this study was to evaluate the expression of the protein annexin A1 (ANXA1), a potent endogenous regulator of the inflammatory process, in ocular toxoplasmosis.Methods: C57BL/ 6 female mice were infected using intravitreal injections of either 10(6) tachyzoites of Toxoplasma gondii (RH strain; T. gondii) or PBS only (control groups). After 24, 48, and 72 h, animals were sacrificed and their eyes were harvested for histopathological, immunohistochemical, and ultrastructural immunocytochemical analysis of ANXA1. Human retinal pigment epithelial (RPE) cells (ARPE-19) were infected in vitro with T. gondii and collected after 60, 120, 240 min, and 24 h.Results: Compared with non-infected eyes, an intense inflammatory response was observed in the anterior (24 h after infection) and posterior segments (72 h after infection) of the infected eye, characterized by neutrophil infiltration and by the presence of tachyzoites and their consequent destruction along with disorganization of normal retina architecture and RPE vacuolization. T. gondii infection was associated with a significant increase of ANXA1 expression in the neutrophils at 24, 48, and 72 h, and in the RPE at 48 and 72 h. In vitro studies confirmed an upregulation of ANXA1 levels in RPE cells, after 60 and 120 min of infection with T. gondii.Conclusions: The positive modulation of endogenous ANXA1 in the inflammatory and RPE cells during T. gondii infection suggests that this protein may serve as a therapeutic target in ocular toxoplasmosis. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-06-15 2018-06-18T11:04:11Z 2018-06-18T11:04:11Z |
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://www.molvis.org/molvis/v18/a163/ Molecular Vision. Atlanta: Molecular Vision, v. 18, n. 163-64, p. 1583-1593, 2012. 1090-0535 http://repositorio.unifesp.br/handle/11600/44936 WOS:000305554600001 |
url |
http://www.molvis.org/molvis/v18/a163/ http://repositorio.unifesp.br/handle/11600/44936 |
identifier_str_mv |
Molecular Vision. Atlanta: Molecular Vision, v. 18, n. 163-64, p. 1583-1593, 2012. 1090-0535 WOS:000305554600001 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Molecular Vision |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1583-1593 |
dc.publisher.none.fl_str_mv |
Molecular Vision |
publisher.none.fl_str_mv |
Molecular Vision |
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 |
_version_ |
1814268321806155776 |