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Similarities and Differences in RANTES- and (AOP)-RANTES–triggered Signals: Implications for Chemotaxis
Chemokines are a family of proinflammatory cytokines that attract and activate specific types of leukocytes. Chemokines mediate their effects via interaction with seven transmembrane G protein–coupled receptors (GPCR). Using CCR5-transfected HEK-293 cells, we show that both the CCR5 ligand, RANTES,...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1999
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132943/ https://www.ncbi.nlm.nih.gov/pubmed/10037796 |
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author | Rodríguez-Frade, José M. Vila-Coro, Antonio J. Martín, Ana Nieto, Marta Sánchez-Madrid, Francisco Proudfoot, Amanda E.I. Wells, Timothy N.C. Martínez-A, Carlos Mellado, Mario |
author_facet | Rodríguez-Frade, José M. Vila-Coro, Antonio J. Martín, Ana Nieto, Marta Sánchez-Madrid, Francisco Proudfoot, Amanda E.I. Wells, Timothy N.C. Martínez-A, Carlos Mellado, Mario |
author_sort | Rodríguez-Frade, José M. |
collection | PubMed |
description | Chemokines are a family of proinflammatory cytokines that attract and activate specific types of leukocytes. Chemokines mediate their effects via interaction with seven transmembrane G protein–coupled receptors (GPCR). Using CCR5-transfected HEK-293 cells, we show that both the CCR5 ligand, RANTES, as well as its derivative, aminooxypentane (AOP)- RANTES, trigger immediate responses such as Ca(2+) influx, receptor dimerization, tyrosine phosphorylation, and Gα(i) as well as JAK/STAT association to the receptor. In contrast to RANTES, (AOP)-RANTES is unable to trigger late responses, as measured by the association of focal adhesion kinase (FAK) to the chemokine receptor complex, impaired cell polarization required for migration, or chemotaxis. The results are discussed in the context of the dissociation of the late signals, provoked by the chemokines required for cell migration, from early signals. |
format | Text |
id | pubmed-2132943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21329432008-05-01 Similarities and Differences in RANTES- and (AOP)-RANTES–triggered Signals: Implications for Chemotaxis Rodríguez-Frade, José M. Vila-Coro, Antonio J. Martín, Ana Nieto, Marta Sánchez-Madrid, Francisco Proudfoot, Amanda E.I. Wells, Timothy N.C. Martínez-A, Carlos Mellado, Mario J Cell Biol Regular Articles Chemokines are a family of proinflammatory cytokines that attract and activate specific types of leukocytes. Chemokines mediate their effects via interaction with seven transmembrane G protein–coupled receptors (GPCR). Using CCR5-transfected HEK-293 cells, we show that both the CCR5 ligand, RANTES, as well as its derivative, aminooxypentane (AOP)- RANTES, trigger immediate responses such as Ca(2+) influx, receptor dimerization, tyrosine phosphorylation, and Gα(i) as well as JAK/STAT association to the receptor. In contrast to RANTES, (AOP)-RANTES is unable to trigger late responses, as measured by the association of focal adhesion kinase (FAK) to the chemokine receptor complex, impaired cell polarization required for migration, or chemotaxis. The results are discussed in the context of the dissociation of the late signals, provoked by the chemokines required for cell migration, from early signals. The Rockefeller University Press 1999-02-22 /pmc/articles/PMC2132943/ /pubmed/10037796 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Regular Articles Rodríguez-Frade, José M. Vila-Coro, Antonio J. Martín, Ana Nieto, Marta Sánchez-Madrid, Francisco Proudfoot, Amanda E.I. Wells, Timothy N.C. Martínez-A, Carlos Mellado, Mario Similarities and Differences in RANTES- and (AOP)-RANTES–triggered Signals: Implications for Chemotaxis |
title | Similarities and Differences in RANTES- and (AOP)-RANTES–triggered Signals: Implications for Chemotaxis |
title_full | Similarities and Differences in RANTES- and (AOP)-RANTES–triggered Signals: Implications for Chemotaxis |
title_fullStr | Similarities and Differences in RANTES- and (AOP)-RANTES–triggered Signals: Implications for Chemotaxis |
title_full_unstemmed | Similarities and Differences in RANTES- and (AOP)-RANTES–triggered Signals: Implications for Chemotaxis |
title_short | Similarities and Differences in RANTES- and (AOP)-RANTES–triggered Signals: Implications for Chemotaxis |
title_sort | similarities and differences in rantes- and (aop)-rantes–triggered signals: implications for chemotaxis |
topic | Regular Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132943/ https://www.ncbi.nlm.nih.gov/pubmed/10037796 |
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