Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions

Detalhes bibliográficos
Autor(a) principal: Machado, Isabel Daufenback
Data de Publicação: 2014
Outros Autores: Santin, Jose Roberto, Drewes, Carine Cristiane, Gil, Cristiane Damas [UNIFESP], Oliani, Sonia Maria, Perretti, Mauro, Poliselli Farsky, Sandra Helena
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
dARK ID: ark:/48912/001300000jd1x
DOI: 10.1152/ajpendo.00227.2014
Texto Completo: http://dx.doi.org/10.1152/ajpendo.00227.2014
http://repositorio.unifesp.br/handle/11600/38366
Resumo: Elevated levels of adrenocorticotrophic hormone (ACTH) mobilize granulocytes from bone marrow into the blood, although these neutrophils are refractory to a full migratory response into inflamed tissues. Here, we investigated the dependence of glucocorticoid receptor activation and glucocorticoid-regulated protein annexin A1 (ANXA1) on ACTH-induced neutrophilia and the phenotype of blood neutrophil after ACTH injection, focusing on adhesion molecule expressions and locomotion properties. ACTH injection (5 mu g ip, 4 h) induced neutrophilia in wild-type (WT) mice and did not alter the elevated numbers of neutrophils in RU-38486 (RU)-pretreated or ANXA1(-/-)mice injected with ACTH. Neutrophils from WT ACTH-treated mice presented higher expression of Ly6G(+) ANXA1(high), CD18(high), CD62L(high), CD49(high), CXCR4(high), and formyl-peptide receptor 1 (FPR1(low)) than those observed in RU-pretreated or ANXA1(-/-)mice. the membrane phenotype of neutrophils collected from WT ACTH-treated mice was paralleled by elevated fractions of rolling and adherent leukocytes to the cremaster postcapillary venules together with impaired neutrophil migration into inflamed air pouches in vivo and in vitro reduced formyl-methionyl-leucyl-phenylalanine (fMLP) or stromal-derived factor-1 (SDF-1 alpha)-induced chemotaxis. in an 18-h senescence protocol, neutrophils from WT ACTH-treated mice had a higher proportion of ANXAV(low)/CXCR4(low), and they were less phagocytosed by peritoneal macrophages. We conclude that alterations on HPA axis affect the pattern of membrane receptors in circulating neutrophils, which may lead to different neutrophil phenotypes in the blood. Moreover, ACTH actions render circulating neutrophils to a phenotype with early reactivity, such as in vivo leukocyte-endothelial interactions, but with impaired locomotion and clearance.
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spelling Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actionshypothalamic-pituitary-adrenal axischemokine (C-X-C motif) receptor 4adhesion moleculeschemotaxisintravital microscopyElevated levels of adrenocorticotrophic hormone (ACTH) mobilize granulocytes from bone marrow into the blood, although these neutrophils are refractory to a full migratory response into inflamed tissues. Here, we investigated the dependence of glucocorticoid receptor activation and glucocorticoid-regulated protein annexin A1 (ANXA1) on ACTH-induced neutrophilia and the phenotype of blood neutrophil after ACTH injection, focusing on adhesion molecule expressions and locomotion properties. ACTH injection (5 mu g ip, 4 h) induced neutrophilia in wild-type (WT) mice and did not alter the elevated numbers of neutrophils in RU-38486 (RU)-pretreated or ANXA1(-/-)mice injected with ACTH. Neutrophils from WT ACTH-treated mice presented higher expression of Ly6G(+) ANXA1(high), CD18(high), CD62L(high), CD49(high), CXCR4(high), and formyl-peptide receptor 1 (FPR1(low)) than those observed in RU-pretreated or ANXA1(-/-)mice. the membrane phenotype of neutrophils collected from WT ACTH-treated mice was paralleled by elevated fractions of rolling and adherent leukocytes to the cremaster postcapillary venules together with impaired neutrophil migration into inflamed air pouches in vivo and in vitro reduced formyl-methionyl-leucyl-phenylalanine (fMLP) or stromal-derived factor-1 (SDF-1 alpha)-induced chemotaxis. in an 18-h senescence protocol, neutrophils from WT ACTH-treated mice had a higher proportion of ANXAV(low)/CXCR4(low), and they were less phagocytosed by peritoneal macrophages. We conclude that alterations on HPA axis affect the pattern of membrane receptors in circulating neutrophils, which may lead to different neutrophil phenotypes in the blood. Moreover, ACTH actions render circulating neutrophils to a phenotype with early reactivity, such as in vivo leukocyte-endothelial interactions, but with impaired locomotion and clearance.Univ São Paulo, Fac Pharmaceut Sci, Dept Clin & Toxicol Analyses, BR-05508900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morphol & Genet, São Paulo, BrazilSão Paulo State Univ, Inst Biociencias Letras & Ciencias Exatas, Dept Biol, Sao Jose Do Rio Preto, BrazilQueen Mary Univ London, Barts & London Sch Med, William Harvey Res Inst, London, EnglandUniversidade Federal de São Paulo, Dept Morphol & Genet, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)FAPESP: 2010/16828-0: 2010/08402-2: 2010/17175-0: 2010/19802-1Amer Physiological SocUniversidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)São Paulo State UnivQueen Mary Univ LondonMachado, Isabel DaufenbackSantin, Jose RobertoDrewes, Carine CristianeGil, Cristiane Damas [UNIFESP]Oliani, Sonia MariaPerretti, MauroPoliselli Farsky, Sandra Helena2016-01-24T14:38:03Z2016-01-24T14:38:03Z2014-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionE754-E763http://dx.doi.org/10.1152/ajpendo.00227.2014American Journal of Physiology-endocrinology and Metabolism. Bethesda: Amer Physiological Soc, v. 307, n. 9, p. E754-E763, 2014.10.1152/ajpendo.00227.20140193-1849http://repositorio.unifesp.br/handle/11600/38366WOS:000344989400003ark:/48912/001300000jd1xengAmerican Journal of Physiology-endocrinology and Metabolisminfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2023-05-18T14:58:11Zoai:repositorio.unifesp.br/:11600/38366Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:21:02.610485Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
title Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
spellingShingle Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
Machado, Isabel Daufenback
hypothalamic-pituitary-adrenal axis
chemokine (C-X-C motif) receptor 4
adhesion molecules
chemotaxis
intravital microscopy
Machado, Isabel Daufenback
hypothalamic-pituitary-adrenal axis
chemokine (C-X-C motif) receptor 4
adhesion molecules
chemotaxis
intravital microscopy
title_short Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
title_full Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
title_fullStr Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
title_full_unstemmed Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
title_sort Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
author Machado, Isabel Daufenback
author_facet Machado, Isabel Daufenback
Machado, Isabel Daufenback
Santin, Jose Roberto
Drewes, Carine Cristiane
Gil, Cristiane Damas [UNIFESP]
Oliani, Sonia Maria
Perretti, Mauro
Poliselli Farsky, Sandra Helena
Santin, Jose Roberto
Drewes, Carine Cristiane
Gil, Cristiane Damas [UNIFESP]
Oliani, Sonia Maria
Perretti, Mauro
Poliselli Farsky, Sandra Helena
author_role author
author2 Santin, Jose Roberto
Drewes, Carine Cristiane
Gil, Cristiane Damas [UNIFESP]
Oliani, Sonia Maria
Perretti, Mauro
Poliselli Farsky, Sandra Helena
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
São Paulo State Univ
Queen Mary Univ London
dc.contributor.author.fl_str_mv Machado, Isabel Daufenback
Santin, Jose Roberto
Drewes, Carine Cristiane
Gil, Cristiane Damas [UNIFESP]
Oliani, Sonia Maria
Perretti, Mauro
Poliselli Farsky, Sandra Helena
dc.subject.por.fl_str_mv hypothalamic-pituitary-adrenal axis
chemokine (C-X-C motif) receptor 4
adhesion molecules
chemotaxis
intravital microscopy
topic hypothalamic-pituitary-adrenal axis
chemokine (C-X-C motif) receptor 4
adhesion molecules
chemotaxis
intravital microscopy
description Elevated levels of adrenocorticotrophic hormone (ACTH) mobilize granulocytes from bone marrow into the blood, although these neutrophils are refractory to a full migratory response into inflamed tissues. Here, we investigated the dependence of glucocorticoid receptor activation and glucocorticoid-regulated protein annexin A1 (ANXA1) on ACTH-induced neutrophilia and the phenotype of blood neutrophil after ACTH injection, focusing on adhesion molecule expressions and locomotion properties. ACTH injection (5 mu g ip, 4 h) induced neutrophilia in wild-type (WT) mice and did not alter the elevated numbers of neutrophils in RU-38486 (RU)-pretreated or ANXA1(-/-)mice injected with ACTH. Neutrophils from WT ACTH-treated mice presented higher expression of Ly6G(+) ANXA1(high), CD18(high), CD62L(high), CD49(high), CXCR4(high), and formyl-peptide receptor 1 (FPR1(low)) than those observed in RU-pretreated or ANXA1(-/-)mice. the membrane phenotype of neutrophils collected from WT ACTH-treated mice was paralleled by elevated fractions of rolling and adherent leukocytes to the cremaster postcapillary venules together with impaired neutrophil migration into inflamed air pouches in vivo and in vitro reduced formyl-methionyl-leucyl-phenylalanine (fMLP) or stromal-derived factor-1 (SDF-1 alpha)-induced chemotaxis. in an 18-h senescence protocol, neutrophils from WT ACTH-treated mice had a higher proportion of ANXAV(low)/CXCR4(low), and they were less phagocytosed by peritoneal macrophages. We conclude that alterations on HPA axis affect the pattern of membrane receptors in circulating neutrophils, which may lead to different neutrophil phenotypes in the blood. Moreover, ACTH actions render circulating neutrophils to a phenotype with early reactivity, such as in vivo leukocyte-endothelial interactions, but with impaired locomotion and clearance.
publishDate 2014
dc.date.none.fl_str_mv 2014-11-01
2016-01-24T14:38:03Z
2016-01-24T14:38:03Z
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/10.1152/ajpendo.00227.2014
American Journal of Physiology-endocrinology and Metabolism. Bethesda: Amer Physiological Soc, v. 307, n. 9, p. E754-E763, 2014.
10.1152/ajpendo.00227.2014
0193-1849
http://repositorio.unifesp.br/handle/11600/38366
WOS:000344989400003
dc.identifier.dark.fl_str_mv ark:/48912/001300000jd1x
url http://dx.doi.org/10.1152/ajpendo.00227.2014
http://repositorio.unifesp.br/handle/11600/38366
identifier_str_mv American Journal of Physiology-endocrinology and Metabolism. Bethesda: Amer Physiological Soc, v. 307, n. 9, p. E754-E763, 2014.
10.1152/ajpendo.00227.2014
0193-1849
WOS:000344989400003
ark:/48912/001300000jd1x
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv American Journal of Physiology-endocrinology and Metabolism
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv E754-E763
dc.publisher.none.fl_str_mv Amer Physiological Soc
publisher.none.fl_str_mv Amer Physiological Soc
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_ 1822219212787023872
dc.identifier.doi.none.fl_str_mv 10.1152/ajpendo.00227.2014