Mast cells modulate the inflammatory process in endotoxin-induced uveitis

Detalhes bibliográficos
Autor(a) principal: Silva, Pierre Sebastiao da [UNIFESP]
Data de Publicação: 2011
Outros Autores: Girol, Ana Paula, Oliani, Sonia Maria [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/11600/44935
http://www.molvis.org/molvis/v17/a147/
Resumo: Purpose: To investigate the role of mast cells and annexin-A1 (Anxa1) in endotoxin-induced uveitis (EIU).Methods: EIU was induced by injection of lipopolysaccharide (LPS) into the paws of rats, which were then sacrificed after 24 and 48 h. To assess EIU in the absence of mast cells, groups of animals were pretreated with compound 48/80 (c48/80) and sacrificed after 24 h after no treatment or EIU induction. The eyes were used for histological studies and the aqueous humor (AqH) pool was used for the analysis of transmigrated cells and Anxa1 levels. In inflammatory cells, Anxa1 expression was monitored by immunohistochemistry.Results: After 24 h, rats with EIU exhibited degranulated mast cells, associated with elevated numbers of infiltrating leukocytes and the high expression of Anxa1 in the AqH and the neutrophils. After 48 h of EIU, the mast cells were intact, indicating granule re-synthesis, and there was a reduction of neutrophil transmigration and an increase in the number of mononuclear phagocytic cells in ocular tissues. Anxa1 expression was decreased in neutrophils but increased in mononuclear phagocytic cells. In the animals pretreated with c48/80 and subjected to EIU, mast cells responded to this secretagogue by degranulating and few transmigrated neutrophils were observed.Conclustions: We report that mast cells are a potential source of pharmacological mediators that are strongly linked to the pathophysiology of EIU, and the endogenous protein Anxa1 is a mediator in the homeostasis of the inflammatory process with anti-migratory effects on leukocytes, which supports further studies of this protein as an innovative therapy for uveitis.
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spelling Silva, Pierre Sebastiao da [UNIFESP]Girol, Ana PaulaOliani, Sonia Maria [UNIFESP]UNESPUniversidade Federal de São Paulo (UNIFESP)2018-06-18T11:04:11Z2018-06-18T11:04:11Z2011-05-08Molecular Vision. Atlanta: Molecular Vision, v. 17, n. 147, p. 1310-1319, 2011.1090-0535http://repositorio.unifesp.br/11600/44935http://www.molvis.org/molvis/v17/a147/WOS:000290297300001Purpose: To investigate the role of mast cells and annexin-A1 (Anxa1) in endotoxin-induced uveitis (EIU).Methods: EIU was induced by injection of lipopolysaccharide (LPS) into the paws of rats, which were then sacrificed after 24 and 48 h. To assess EIU in the absence of mast cells, groups of animals were pretreated with compound 48/80 (c48/80) and sacrificed after 24 h after no treatment or EIU induction. The eyes were used for histological studies and the aqueous humor (AqH) pool was used for the analysis of transmigrated cells and Anxa1 levels. In inflammatory cells, Anxa1 expression was monitored by immunohistochemistry.Results: After 24 h, rats with EIU exhibited degranulated mast cells, associated with elevated numbers of infiltrating leukocytes and the high expression of Anxa1 in the AqH and the neutrophils. After 48 h of EIU, the mast cells were intact, indicating granule re-synthesis, and there was a reduction of neutrophil transmigration and an increase in the number of mononuclear phagocytic cells in ocular tissues. Anxa1 expression was decreased in neutrophils but increased in mononuclear phagocytic cells. In the animals pretreated with c48/80 and subjected to EIU, mast cells responded to this secretagogue by degranulating and few transmigrated neutrophils were observed.Conclustions: We report that mast cells are a potential source of pharmacological mediators that are strongly linked to the pathophysiology of EIU, and the endogenous protein Anxa1 is a mediator in the homeostasis of the inflammatory process with anti-migratory effects on leukocytes, which supports further studies of this protein as an innovative therapy for uveitis.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)UNESP, IBILCE, Dept Biol, BR-15054000 Sao Jose Do Rio Preto, SP, BrazilUniv Fed Sao Paulo, Sao Paulo, BrazilUniv Fed Sao Paulo, Sao Paulo, BrazilCNPq: 306074/2007-9FAPESP: 06/54095-9Web of Science1310-1319engMolecular VisionMolecular VisionMast cells modulate the inflammatory process in endotoxin-induced uveitisinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/449352021-10-05 22:12:42.955metadata only accessoai:repositorio.unifesp.br:11600/44935Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652021-10-06T01:12:42Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Mast cells modulate the inflammatory process in endotoxin-induced uveitis
title Mast cells modulate the inflammatory process in endotoxin-induced uveitis
spellingShingle Mast cells modulate the inflammatory process in endotoxin-induced uveitis
Silva, Pierre Sebastiao da [UNIFESP]
title_short Mast cells modulate the inflammatory process in endotoxin-induced uveitis
title_full Mast cells modulate the inflammatory process in endotoxin-induced uveitis
title_fullStr Mast cells modulate the inflammatory process in endotoxin-induced uveitis
title_full_unstemmed Mast cells modulate the inflammatory process in endotoxin-induced uveitis
title_sort Mast cells modulate the inflammatory process in endotoxin-induced uveitis
author Silva, Pierre Sebastiao da [UNIFESP]
author_facet Silva, Pierre Sebastiao da [UNIFESP]
Girol, Ana Paula
Oliani, Sonia Maria [UNIFESP]
author_role author
author2 Girol, Ana Paula
Oliani, Sonia Maria [UNIFESP]
author2_role author
author
dc.contributor.institution.none.fl_str_mv UNESP
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Silva, Pierre Sebastiao da [UNIFESP]
Girol, Ana Paula
Oliani, Sonia Maria [UNIFESP]
description Purpose: To investigate the role of mast cells and annexin-A1 (Anxa1) in endotoxin-induced uveitis (EIU).Methods: EIU was induced by injection of lipopolysaccharide (LPS) into the paws of rats, which were then sacrificed after 24 and 48 h. To assess EIU in the absence of mast cells, groups of animals were pretreated with compound 48/80 (c48/80) and sacrificed after 24 h after no treatment or EIU induction. The eyes were used for histological studies and the aqueous humor (AqH) pool was used for the analysis of transmigrated cells and Anxa1 levels. In inflammatory cells, Anxa1 expression was monitored by immunohistochemistry.Results: After 24 h, rats with EIU exhibited degranulated mast cells, associated with elevated numbers of infiltrating leukocytes and the high expression of Anxa1 in the AqH and the neutrophils. After 48 h of EIU, the mast cells were intact, indicating granule re-synthesis, and there was a reduction of neutrophil transmigration and an increase in the number of mononuclear phagocytic cells in ocular tissues. Anxa1 expression was decreased in neutrophils but increased in mononuclear phagocytic cells. In the animals pretreated with c48/80 and subjected to EIU, mast cells responded to this secretagogue by degranulating and few transmigrated neutrophils were observed.Conclustions: We report that mast cells are a potential source of pharmacological mediators that are strongly linked to the pathophysiology of EIU, and the endogenous protein Anxa1 is a mediator in the homeostasis of the inflammatory process with anti-migratory effects on leukocytes, which supports further studies of this protein as an innovative therapy for uveitis.
publishDate 2011
dc.date.issued.fl_str_mv 2011-05-08
dc.date.accessioned.fl_str_mv 2018-06-18T11:04:11Z
dc.date.available.fl_str_mv 2018-06-18T11:04:11Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Molecular Vision. Atlanta: Molecular Vision, v. 17, n. 147, p. 1310-1319, 2011.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/11600/44935
http://www.molvis.org/molvis/v17/a147/
dc.identifier.issn.none.fl_str_mv 1090-0535
dc.identifier.wos.none.fl_str_mv WOS:000290297300001
identifier_str_mv Molecular Vision. Atlanta: Molecular Vision, v. 17, n. 147, p. 1310-1319, 2011.
1090-0535
WOS:000290297300001
url http://repositorio.unifesp.br/11600/44935
http://www.molvis.org/molvis/v17/a147/
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.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 1310-1319
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
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