Mast cells modulate the inflammatory process in endotoxin-induced uveitis
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://hdl.handle.net/11449/195973 |
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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Mast cells modulate the inflammatory process in endotoxin-induced uveitisPurpose: 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, BrazilUNESP, IBILCE, Dept Biol, BR-15054000 Sao Jose Do Rio Preto, SP, BrazilCNPq: 306074/2007-9FAPESP: 06/54095-9Molecular VisionUniversidade Estadual Paulista (Unesp)Universidade Federal de São Paulo (UNIFESP)Silva, Pierre Sebastiao daGirol, Ana Paula [UNESP]Oliani, Sonia M. [UNESP]2020-12-10T19:00:03Z2020-12-10T19:00:03Z2011-05-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1310-1319Molecular Vision. Atlanta: Molecular Vision, v. 17, n. 147, p. 1310-1319, 2011.1090-0535http://hdl.handle.net/11449/195973WOS:000290297300001Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMolecular Visioninfo:eu-repo/semantics/openAccess2021-10-22T20:49:10Zoai:repositorio.unesp.br:11449/195973Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:32:41.539542Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.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 |
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 |
author_facet |
Silva, Pierre Sebastiao da Girol, Ana Paula [UNESP] Oliani, Sonia M. [UNESP] |
author_role |
author |
author2 |
Girol, Ana Paula [UNESP] Oliani, Sonia M. [UNESP] |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Silva, Pierre Sebastiao da Girol, Ana Paula [UNESP] Oliani, Sonia M. [UNESP] |
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.none.fl_str_mv |
2011-05-08 2020-12-10T19:00:03Z 2020-12-10T19:00:03Z |
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.uri.fl_str_mv |
Molecular Vision. Atlanta: Molecular Vision, v. 17, n. 147, p. 1310-1319, 2011. 1090-0535 http://hdl.handle.net/11449/195973 WOS:000290297300001 |
identifier_str_mv |
Molecular Vision. Atlanta: Molecular Vision, v. 17, n. 147, p. 1310-1319, 2011. 1090-0535 WOS:000290297300001 |
url |
http://hdl.handle.net/11449/195973 |
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 |
1310-1319 |
dc.publisher.none.fl_str_mv |
Molecular Vision |
publisher.none.fl_str_mv |
Molecular Vision |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129216885030912 |