Regulation of MMP-3 expression and secretion by the chemokine eotaxin-1 in human chondrocytes
<p>Abstract</p> <p>Background</p> <p>Osteoarthritis (OA) is characterized by the degradation of articular cartilage, marked by the breakdown of matrix proteins. Studies demonstrated the involvement of chemokines in this process, and some may potentially serve as diagnos...
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doaj-224670af496b4eaba28af1847c695c822020-11-25T00:58:03ZengBMCJournal of Biomedical Science1021-77701423-01272011-11-011818610.1186/1423-0127-18-86Regulation of MMP-3 expression and secretion by the chemokine eotaxin-1 in human chondrocytesChao Pin-ZhirHsieh Ming-ShiumCheng Chao-WenLin Yung-FengChen Chien-Ho<p>Abstract</p> <p>Background</p> <p>Osteoarthritis (OA) is characterized by the degradation of articular cartilage, marked by the breakdown of matrix proteins. Studies demonstrated the involvement of chemokines in this process, and some may potentially serve as diagnostic markers and therapeutic targets; however, the underlying signal transductions are not well understood.</p> <p>Methods</p> <p>We investigated the effects of the CC chemokine eotaxin-1 (CCL11) on the matrix metalloproteinase (MMP) expression and secretion in the human chondrocyte cell line SW1353 and primary chondrocytes.</p> <p>Results</p> <p>Eotaxin-1 significantly induced MMP-3 mRNA expression in a dose-dependent manner. Inhibitors of extracellular signal-regulated kinase (ERK) and p38 kinase were able to repress eotaxin-1-induced MMP-3 expression. On the contrary, Rp-adenosine-3',5'-cyclic monophosphorothioate (Rp-cAMPs), a competitive cAMP antagonist for cAMP receptors, and H-89, a protein kinase A (PKA) inhibitor, markedly enhanced eotaxin-1-induced MMP-3 expression. These results suggest that MMP-3 expression is specifically mediated by the G protein-coupled eotaxin-1 receptor activities. Interestingly, little amount of MMP-3 protein was detected in the cell lysates of eotaxin-1-treated SW1353 cells, and most of MMP-3 protein was in the culture media. Furthermore we found that the eotaxin-1-dependent MMP-3 protein secretion was regulated by phospholipase C (PLC)-protein kinase C (PKC) cascade and c-Jun N-terminal kinase (JNK)/mitogen-activated protein (MAP) kinase pathways. These data indicate a specific regulation of MMP-3 secretion also by eotaxin-1 receptor activities.</p> <p>Conclusions</p> <p>Eotaxin-1 not only induces MMP-3 gene expression but also promotes MMP-3 protein secretion through G protein-coupled eotaxin-1 receptor activities. Chemokines, such as eotaxin-1, could be a potential candidate in the diagnosis and treatment of arthritis.</p> http://www.jbiomedsci.com/content/18/1/86osteoarthritischemokinecartilage degradationchondrocyteMMP-3eotaxin-1 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chao Pin-Zhir Hsieh Ming-Shium Cheng Chao-Wen Lin Yung-Feng Chen Chien-Ho |
spellingShingle |
Chao Pin-Zhir Hsieh Ming-Shium Cheng Chao-Wen Lin Yung-Feng Chen Chien-Ho Regulation of MMP-3 expression and secretion by the chemokine eotaxin-1 in human chondrocytes Journal of Biomedical Science osteoarthritis chemokine cartilage degradation chondrocyte MMP-3 eotaxin-1 |
author_facet |
Chao Pin-Zhir Hsieh Ming-Shium Cheng Chao-Wen Lin Yung-Feng Chen Chien-Ho |
author_sort |
Chao Pin-Zhir |
title |
Regulation of MMP-3 expression and secretion by the chemokine eotaxin-1 in human chondrocytes |
title_short |
Regulation of MMP-3 expression and secretion by the chemokine eotaxin-1 in human chondrocytes |
title_full |
Regulation of MMP-3 expression and secretion by the chemokine eotaxin-1 in human chondrocytes |
title_fullStr |
Regulation of MMP-3 expression and secretion by the chemokine eotaxin-1 in human chondrocytes |
title_full_unstemmed |
Regulation of MMP-3 expression and secretion by the chemokine eotaxin-1 in human chondrocytes |
title_sort |
regulation of mmp-3 expression and secretion by the chemokine eotaxin-1 in human chondrocytes |
publisher |
BMC |
series |
Journal of Biomedical Science |
issn |
1021-7770 1423-0127 |
publishDate |
2011-11-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Osteoarthritis (OA) is characterized by the degradation of articular cartilage, marked by the breakdown of matrix proteins. Studies demonstrated the involvement of chemokines in this process, and some may potentially serve as diagnostic markers and therapeutic targets; however, the underlying signal transductions are not well understood.</p> <p>Methods</p> <p>We investigated the effects of the CC chemokine eotaxin-1 (CCL11) on the matrix metalloproteinase (MMP) expression and secretion in the human chondrocyte cell line SW1353 and primary chondrocytes.</p> <p>Results</p> <p>Eotaxin-1 significantly induced MMP-3 mRNA expression in a dose-dependent manner. Inhibitors of extracellular signal-regulated kinase (ERK) and p38 kinase were able to repress eotaxin-1-induced MMP-3 expression. On the contrary, Rp-adenosine-3',5'-cyclic monophosphorothioate (Rp-cAMPs), a competitive cAMP antagonist for cAMP receptors, and H-89, a protein kinase A (PKA) inhibitor, markedly enhanced eotaxin-1-induced MMP-3 expression. These results suggest that MMP-3 expression is specifically mediated by the G protein-coupled eotaxin-1 receptor activities. Interestingly, little amount of MMP-3 protein was detected in the cell lysates of eotaxin-1-treated SW1353 cells, and most of MMP-3 protein was in the culture media. Furthermore we found that the eotaxin-1-dependent MMP-3 protein secretion was regulated by phospholipase C (PLC)-protein kinase C (PKC) cascade and c-Jun N-terminal kinase (JNK)/mitogen-activated protein (MAP) kinase pathways. These data indicate a specific regulation of MMP-3 secretion also by eotaxin-1 receptor activities.</p> <p>Conclusions</p> <p>Eotaxin-1 not only induces MMP-3 gene expression but also promotes MMP-3 protein secretion through G protein-coupled eotaxin-1 receptor activities. Chemokines, such as eotaxin-1, could be a potential candidate in the diagnosis and treatment of arthritis.</p> |
topic |
osteoarthritis chemokine cartilage degradation chondrocyte MMP-3 eotaxin-1 |
url |
http://www.jbiomedsci.com/content/18/1/86 |
work_keys_str_mv |
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