In vitro and in vivo studies on CCR10 regulation by Annexin A1
Autor(a) principal: | |
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Data de Publicação: | 2006 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.febslet.2006.01.072 http://hdl.handle.net/11449/21716 |
Resumo: | The mode of action of annexin A1 (ANXA1) is poorly understood. By using rapid subtraction hybridization we studied the effects of human recombinant ANXA1 and the N-terminal ANXA1 peptide on gene expression in a human larynx cell line. Three genes showed strong downregulation after treatment with ANXA1. In contrast, expression of CCR10, a seven transmembrane G-protein coupled receptor for chemokine CCL27 involved in mucosal immunity, was increased. Moreover the reduction in CCR10 expression induced by ANXA1 gene deletion was rescued by intravenous treatment with low doses of ANXA1. These findings provide new evidence that ANXA1 modulates gene expression. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved. |
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In vitro and in vivo studies on CCR10 regulation by Annexin A1gene expressionhost defenceannexin A1-null miceepithelial cellsannexin A1The mode of action of annexin A1 (ANXA1) is poorly understood. By using rapid subtraction hybridization we studied the effects of human recombinant ANXA1 and the N-terminal ANXA1 peptide on gene expression in a human larynx cell line. Three genes showed strong downregulation after treatment with ANXA1. In contrast, expression of CCR10, a seven transmembrane G-protein coupled receptor for chemokine CCL27 involved in mucosal immunity, was increased. Moreover the reduction in CCR10 expression induced by ANXA1 gene deletion was rescued by intravenous treatment with low doses of ANXA1. These findings provide new evidence that ANXA1 modulates gene expression. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Neurosci & Mental Hlth, Dept Cellular & Mol Neurosci, London W12 0NN, EnglandUNESP, São Paulo State Univ, IBILCE, Sao Jose do Rio Preto, SP, BrazilUSP, Fac Med, Ribeirao Preto, BrazilUNESP, São Paulo State Univ, IBILCE, Sao Jose do Rio Preto, SP, BrazilElsevier B.V.Univ London Imperial Coll Sci Technol & MedUniversidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Rodrigues-Lisoni, F. C.Mehemet, D. K.Peitl, P.John, C. D.Tajara, E.Buckingham, J. C.Solito, E.2014-05-20T14:01:32Z2014-05-20T14:01:32Z2006-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1431-1438application/pdfhttp://dx.doi.org/10.1016/j.febslet.2006.01.072Febs Letters. Amsterdam: Elsevier B.V., v. 580, n. 5, p. 1431-1438, 2006.0014-5793http://hdl.handle.net/11449/2171610.1016/j.febslet.2006.01.072WOS:000235597700037WOS000235597700037.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengFEBS Letters1,991info:eu-repo/semantics/openAccess2023-12-24T06:17:13Zoai:repositorio.unesp.br:11449/21716Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:10:13.225239Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
In vitro and in vivo studies on CCR10 regulation by Annexin A1 |
title |
In vitro and in vivo studies on CCR10 regulation by Annexin A1 |
spellingShingle |
In vitro and in vivo studies on CCR10 regulation by Annexin A1 Rodrigues-Lisoni, F. C. gene expression host defence annexin A1-null mice epithelial cells annexin A1 |
title_short |
In vitro and in vivo studies on CCR10 regulation by Annexin A1 |
title_full |
In vitro and in vivo studies on CCR10 regulation by Annexin A1 |
title_fullStr |
In vitro and in vivo studies on CCR10 regulation by Annexin A1 |
title_full_unstemmed |
In vitro and in vivo studies on CCR10 regulation by Annexin A1 |
title_sort |
In vitro and in vivo studies on CCR10 regulation by Annexin A1 |
author |
Rodrigues-Lisoni, F. C. |
author_facet |
Rodrigues-Lisoni, F. C. Mehemet, D. K. Peitl, P. John, C. D. Tajara, E. Buckingham, J. C. Solito, E. |
author_role |
author |
author2 |
Mehemet, D. K. Peitl, P. John, C. D. Tajara, E. Buckingham, J. C. Solito, E. |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Univ London Imperial Coll Sci Technol & Med Universidade Estadual Paulista (Unesp) Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Rodrigues-Lisoni, F. C. Mehemet, D. K. Peitl, P. John, C. D. Tajara, E. Buckingham, J. C. Solito, E. |
dc.subject.por.fl_str_mv |
gene expression host defence annexin A1-null mice epithelial cells annexin A1 |
topic |
gene expression host defence annexin A1-null mice epithelial cells annexin A1 |
description |
The mode of action of annexin A1 (ANXA1) is poorly understood. By using rapid subtraction hybridization we studied the effects of human recombinant ANXA1 and the N-terminal ANXA1 peptide on gene expression in a human larynx cell line. Three genes showed strong downregulation after treatment with ANXA1. In contrast, expression of CCR10, a seven transmembrane G-protein coupled receptor for chemokine CCL27 involved in mucosal immunity, was increased. Moreover the reduction in CCR10 expression induced by ANXA1 gene deletion was rescued by intravenous treatment with low doses of ANXA1. These findings provide new evidence that ANXA1 modulates gene expression. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved. |
publishDate |
2006 |
dc.date.none.fl_str_mv |
2006-02-01 2014-05-20T14:01:32Z 2014-05-20T14:01:32Z |
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 |
http://dx.doi.org/10.1016/j.febslet.2006.01.072 Febs Letters. Amsterdam: Elsevier B.V., v. 580, n. 5, p. 1431-1438, 2006. 0014-5793 http://hdl.handle.net/11449/21716 10.1016/j.febslet.2006.01.072 WOS:000235597700037 WOS000235597700037.pdf |
url |
http://dx.doi.org/10.1016/j.febslet.2006.01.072 http://hdl.handle.net/11449/21716 |
identifier_str_mv |
Febs Letters. Amsterdam: Elsevier B.V., v. 580, n. 5, p. 1431-1438, 2006. 0014-5793 10.1016/j.febslet.2006.01.072 WOS:000235597700037 WOS000235597700037.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
FEBS Letters 1,991 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1431-1438 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
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_ |
1808129293367115776 |