Effects of prostaglandin E2 on matrix metalloproteinase-2 activity in synovial cells and its signaling pathway
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Effects of prostaglandin E2 on matrix metalloproteinase-2 activity in synovial cells and its signaling pathway
Journal of Chongqing Medical UniversityVol. 37, Issue 8, Pages: 682-686(2012)
作者机构:
1. 重庆医科大学附属第一医院骨科,重庆,400016
2. 重庆大学生物工程学院与国家“111计划”基地,重庆,400044
3. 美国加州大学圣迭亚哥分校骨科与生物工程系,圣迭亚哥 CA,92093-0412
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Published:2012,
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CHEN Rongfu, HUANG Wei, LIANG Xi, et al. Effects of prostaglandin E2 on matrix metalloproteinase-2 activity in synovial cells and its signaling pathway. [J]. Journal of Chongqing Medical University 37(8):682-686(2012)
DOI:
CHEN Rongfu, HUANG Wei, LIANG Xi, et al. Effects of prostaglandin E2 on matrix metalloproteinase-2 activity in synovial cells and its signaling pathway. [J]. Journal of Chongqing Medical University 37(8):682-686(2012)DOI:
Effects of prostaglandin E2 on matrix metalloproteinase-2 activity in synovial cells and its signaling pathway
Objective:To investigate the effects of prostaglandin E2(PGE2) on matrix metalloproteinase-2(MMP-2) activity in syn-ovial cells and its signaling pathway so as to help discuss the possible effect of PGE2 on the healing ability of anterior cruciate liga-ment(ACL) after injury. Methods:Cultured synovial cells were treated with different concentrations of PGE2,and gelatin zymography assay was performed to detect MMP-2 activity at 12,24,48 h and 72 h after treatment.In presence of 10 ng/ml PGE2,each of seven signal pathway-specific inhibitors was respectively used to treat the synovial cells and MMP-2 activity was detected and semi-quan-tified. Results:PGE2 significantly elevated MMP-2 activity in synovial cells in a dose and time dependent manner. Inhibition of the p38 pathway with SB203850,ERK pathway with PD98059,and PKA pathway with KT5720 had no specific effect on PGE2-induced MMP-2 activity. However,inhibition of the JNK pathway with SP600125,AP-1 pathway with Curcumin,and nuclear factor-κB(NF-κB) pathway with Bay11-7082 and-7085 dramatically decreased PGE2-induced MMP-2 activity to 43%,25%,16% and 11%,respec-tively(P<0.01). Conclusions:PGE2-induced MMP-2 activity in synovial cells may account for ACL’s poor healing ability after in-jury and this process might be regulated via JNK,AP-1 and NF-κB pathway. Inhibition of NF-κB pathway has the strongest decreas-ing effect on PGE2-induced MMP-2 activity,which provides a novel strategy for ACL repair.
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