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CCL2 induces articular chondrocyte MMP expression through ERK and p38 signaling pathways
OBJECTIVE: In previous studies, we determined an association between increased serum and articular cartilage levels of CCL2 with osteoarthritis (OA) progression, cartilage damage and increased MMP13 in cartilage. Here we analyzed CCL2 downstream signaling mediators that lead to gene expression of ca...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718225/ https://www.ncbi.nlm.nih.gov/pubmed/36475068 http://dx.doi.org/10.1016/j.ocarto.2020.100136 |
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author | Willcockson, Helen Ozkan, Huseyin Chubinskaya, Susan Loeser, Richard F. Longobardi, Lara |
author_facet | Willcockson, Helen Ozkan, Huseyin Chubinskaya, Susan Loeser, Richard F. Longobardi, Lara |
author_sort | Willcockson, Helen |
collection | PubMed |
description | OBJECTIVE: In previous studies, we determined an association between increased serum and articular cartilage levels of CCL2 with osteoarthritis (OA) progression, cartilage damage and increased MMP13 in cartilage. Here we analyzed CCL2 downstream signaling mediators that lead to gene expression of cartilage catabolic markers, in healthy and OA human articular chondrocytes. DESIGN: Human articular chondrocytes obtained from healthy or OA subjects were treated with or without recombinant human CCL2; cell lysates or mRNA were collected for immunoblotting or qRT-PCR. For pathway analysis, chondrocytes were pre-incubated with an inhibitor of CCR2 (the unique CCL2 receptor), ERK inhibitor or p38 inhibitor prior to CCL2 treatment. RESULTS: CCL2 treatment of both healthy and OA chondrocytes activated ERK and p38 via CCR2. In healthy chondrocytes, short (6h) and prolonged (24–72h) CCL2 treatments led to Ccr2, Mmp-1, Mmp-3, Mmp-13 and Timp1 upregulation. In OA chondrocytes, CCL2 induced expression of Ccr2, Mmp-1 and Mmp-3, but not Mmp1 and Timp1, and only following longer treatments (72h). In both healthy and OA chondrocytes, the CCL2-mediated upregulation of Ccr2 and cartilage catabolic markers was mediated by ERK and p38 signaling. CONCLUSIONS: The triggering of the CCL2/CCR2 axis in articular chondrocytes activates specific MAPK pathways leading to gene expression of cartilage degrading enzymes. However, some differences in the response to CCL2 stimulation are detected in healthy vs OA chondrocytes with respect to the number of activated genes and to the time of exposure to CCL2, suggesting that CCL2 action in articular cartilage may be dependent on OA stage and severity. |
format | Online Article Text |
id | pubmed-9718225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97182252022-12-05 CCL2 induces articular chondrocyte MMP expression through ERK and p38 signaling pathways Willcockson, Helen Ozkan, Huseyin Chubinskaya, Susan Loeser, Richard F. Longobardi, Lara Osteoarthr Cartil Open ORIGINAL PAPER OBJECTIVE: In previous studies, we determined an association between increased serum and articular cartilage levels of CCL2 with osteoarthritis (OA) progression, cartilage damage and increased MMP13 in cartilage. Here we analyzed CCL2 downstream signaling mediators that lead to gene expression of cartilage catabolic markers, in healthy and OA human articular chondrocytes. DESIGN: Human articular chondrocytes obtained from healthy or OA subjects were treated with or without recombinant human CCL2; cell lysates or mRNA were collected for immunoblotting or qRT-PCR. For pathway analysis, chondrocytes were pre-incubated with an inhibitor of CCR2 (the unique CCL2 receptor), ERK inhibitor or p38 inhibitor prior to CCL2 treatment. RESULTS: CCL2 treatment of both healthy and OA chondrocytes activated ERK and p38 via CCR2. In healthy chondrocytes, short (6h) and prolonged (24–72h) CCL2 treatments led to Ccr2, Mmp-1, Mmp-3, Mmp-13 and Timp1 upregulation. In OA chondrocytes, CCL2 induced expression of Ccr2, Mmp-1 and Mmp-3, but not Mmp1 and Timp1, and only following longer treatments (72h). In both healthy and OA chondrocytes, the CCL2-mediated upregulation of Ccr2 and cartilage catabolic markers was mediated by ERK and p38 signaling. CONCLUSIONS: The triggering of the CCL2/CCR2 axis in articular chondrocytes activates specific MAPK pathways leading to gene expression of cartilage degrading enzymes. However, some differences in the response to CCL2 stimulation are detected in healthy vs OA chondrocytes with respect to the number of activated genes and to the time of exposure to CCL2, suggesting that CCL2 action in articular cartilage may be dependent on OA stage and severity. Elsevier 2021-01-06 /pmc/articles/PMC9718225/ /pubmed/36475068 http://dx.doi.org/10.1016/j.ocarto.2020.100136 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | ORIGINAL PAPER Willcockson, Helen Ozkan, Huseyin Chubinskaya, Susan Loeser, Richard F. Longobardi, Lara CCL2 induces articular chondrocyte MMP expression through ERK and p38 signaling pathways |
title | CCL2 induces articular chondrocyte MMP expression through ERK and p38 signaling pathways |
title_full | CCL2 induces articular chondrocyte MMP expression through ERK and p38 signaling pathways |
title_fullStr | CCL2 induces articular chondrocyte MMP expression through ERK and p38 signaling pathways |
title_full_unstemmed | CCL2 induces articular chondrocyte MMP expression through ERK and p38 signaling pathways |
title_short | CCL2 induces articular chondrocyte MMP expression through ERK and p38 signaling pathways |
title_sort | ccl2 induces articular chondrocyte mmp expression through erk and p38 signaling pathways |
topic | ORIGINAL PAPER |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718225/ https://www.ncbi.nlm.nih.gov/pubmed/36475068 http://dx.doi.org/10.1016/j.ocarto.2020.100136 |
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