Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , |
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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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 |