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Adiponectin and Leptin Induce VCAM-1 Expression in Human and Murine Chondrocytes
BACKGROUND: Osteoarthritis (OA) and rheumatoid arthritis (RA), the most common rheumatic diseases, are characterized by irreversible degeneration of the joint tissues. There are several factors involved in the pathogenesis of these diseases including pro-inflammatory cytokines, adipokines and adhesi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526577/ https://www.ncbi.nlm.nih.gov/pubmed/23285079 http://dx.doi.org/10.1371/journal.pone.0052533 |
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author | Conde, Javier Scotece, Morena López, Verónica Gómez, Rodolfo Lago, Francisca Pino, Jesús Gómez-Reino, Juan Jesús Gualillo, Oreste |
author_facet | Conde, Javier Scotece, Morena López, Verónica Gómez, Rodolfo Lago, Francisca Pino, Jesús Gómez-Reino, Juan Jesús Gualillo, Oreste |
author_sort | Conde, Javier |
collection | PubMed |
description | BACKGROUND: Osteoarthritis (OA) and rheumatoid arthritis (RA), the most common rheumatic diseases, are characterized by irreversible degeneration of the joint tissues. There are several factors involved in the pathogenesis of these diseases including pro-inflammatory cytokines, adipokines and adhesion molecules. OBJECTIVE: Up to now, the relationship between adipokines and adhesion molecules at cartilage level was not explored. Thus, the aim of this article was to study the effect of leptin and adiponectin on the expression of VCAM-1 in human and murine chondrocytes. For completeness, intracellular signal transduction pathway was also explored. METHODS: VCAM-1 expression was assessed by quantitative RT-PCR and western blot analysis upon treatment with leptin, adiponectin and other pertinent reagents in cultured human primary chondrocytes. Signal transduction pathways have been explored by using specific pharmacological inhibitors in the adipokine-stimulated human primary chondrocytes and ATDC5 murine chondrocyte cell line. RESULTS: Herein, we demonstrate, for the first time, that leptin and adiponectin increase VCAM-1 expression in human and murine chondrocytes. In addition, both adipokines have additive effect with IL-1β. Finally, we demonstrate that several kinases, including JAK2, PI3K and AMPK are at a play in the intracellular signalling of VCAM-1 induction. CONCLUSIONS: Taken together, our results suggest that leptin and adiponectin could perpetuate cartilage-degrading processes by inducing also factors responsible of leukocyte and monocyte infiltration at inflamed joints. |
format | Online Article Text |
id | pubmed-3526577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35265772013-01-02 Adiponectin and Leptin Induce VCAM-1 Expression in Human and Murine Chondrocytes Conde, Javier Scotece, Morena López, Verónica Gómez, Rodolfo Lago, Francisca Pino, Jesús Gómez-Reino, Juan Jesús Gualillo, Oreste PLoS One Research Article BACKGROUND: Osteoarthritis (OA) and rheumatoid arthritis (RA), the most common rheumatic diseases, are characterized by irreversible degeneration of the joint tissues. There are several factors involved in the pathogenesis of these diseases including pro-inflammatory cytokines, adipokines and adhesion molecules. OBJECTIVE: Up to now, the relationship between adipokines and adhesion molecules at cartilage level was not explored. Thus, the aim of this article was to study the effect of leptin and adiponectin on the expression of VCAM-1 in human and murine chondrocytes. For completeness, intracellular signal transduction pathway was also explored. METHODS: VCAM-1 expression was assessed by quantitative RT-PCR and western blot analysis upon treatment with leptin, adiponectin and other pertinent reagents in cultured human primary chondrocytes. Signal transduction pathways have been explored by using specific pharmacological inhibitors in the adipokine-stimulated human primary chondrocytes and ATDC5 murine chondrocyte cell line. RESULTS: Herein, we demonstrate, for the first time, that leptin and adiponectin increase VCAM-1 expression in human and murine chondrocytes. In addition, both adipokines have additive effect with IL-1β. Finally, we demonstrate that several kinases, including JAK2, PI3K and AMPK are at a play in the intracellular signalling of VCAM-1 induction. CONCLUSIONS: Taken together, our results suggest that leptin and adiponectin could perpetuate cartilage-degrading processes by inducing also factors responsible of leukocyte and monocyte infiltration at inflamed joints. Public Library of Science 2012-12-19 /pmc/articles/PMC3526577/ /pubmed/23285079 http://dx.doi.org/10.1371/journal.pone.0052533 Text en © 2012 Conde et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Conde, Javier Scotece, Morena López, Verónica Gómez, Rodolfo Lago, Francisca Pino, Jesús Gómez-Reino, Juan Jesús Gualillo, Oreste Adiponectin and Leptin Induce VCAM-1 Expression in Human and Murine Chondrocytes |
title | Adiponectin and Leptin Induce VCAM-1 Expression in Human and Murine Chondrocytes |
title_full | Adiponectin and Leptin Induce VCAM-1 Expression in Human and Murine Chondrocytes |
title_fullStr | Adiponectin and Leptin Induce VCAM-1 Expression in Human and Murine Chondrocytes |
title_full_unstemmed | Adiponectin and Leptin Induce VCAM-1 Expression in Human and Murine Chondrocytes |
title_short | Adiponectin and Leptin Induce VCAM-1 Expression in Human and Murine Chondrocytes |
title_sort | adiponectin and leptin induce vcam-1 expression in human and murine chondrocytes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526577/ https://www.ncbi.nlm.nih.gov/pubmed/23285079 http://dx.doi.org/10.1371/journal.pone.0052533 |
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