Wang Yequan, Yang Li, Zhang Jin, Xue Ruyue, Tang Zhenyu, Huang Wei, Jiang Dianming, Tang Xinyan, Chen Peter, Sung K L Paul
111 project Laboratory of Biomechanics and Tissue Repair, College of Bioengineering, Chongqing University, Chongqing 400044, China.
Mol Cell Biomech. 2010 Jun;7(2):105-14.
The anterior cruciate ligament, posterior cruciate ligament, cartilage and meniscus in human knee joint have poor healing ability. Accumulation of MMPs in the joint fluids due to knee injury has been considered as the main reason. Our previous experiments showed that synovium may be the major regulator of MMPs in joint cavity after injury. In this paper, we used human synoviocytes harvested from synovium to determine whether mechanical injury and inflammatory factors will induce MMP-2 production in synoviocytes. With zymography, we found that mechanical compression increased the MMP-2 production by 23% under 6% compressions, 61% under 12% compression and 109% under 14% compressions. In addition, TNF-alpha can also elevate the activity of MMP-2 in a dose dependent manner, while IL-1alpha does not. However, mixture of these two factors dramatically increased MMP-2 production by 201%. In addition, mechanical injury had a strong synergistic effect on MMP-2 production with TNF-alpha, IL-1alpha and their mixture, increasing by 207%, 354% and 468% individually. The generic MMP activity assayrevealed that mechanical compression increased the generic activity. APMA treatment increased the generic activity of MMPs induced by compres-
人体膝关节中的前交叉韧带、后交叉韧带、软骨和半月板愈合能力较差。膝关节损伤导致关节液中基质金属蛋白酶(MMPs)的积累被认为是主要原因。我们之前的实验表明,滑膜可能是损伤后关节腔内MMPs的主要调节因子。在本文中,我们使用从滑膜中获取的人滑膜细胞来确定机械损伤和炎症因子是否会诱导滑膜细胞产生MMP-2。通过酶谱分析,我们发现机械压缩在6%压缩下使MMP-2的产生增加了23%,在12%压缩下增加了61%,在14%压缩下增加了109%。此外,肿瘤坏死因子-α(TNF-α)也能以剂量依赖的方式提高MMP-2的活性,而白细胞介素-1α(IL-1α)则不能。然而,这两种因子的混合物使MMP-2的产生显著增加了201%。此外,机械损伤与TNF-α、IL-1α及其混合物对MMP-2的产生具有强烈的协同作用,分别增加了207%、354%和468%。通用MMP活性测定显示机械压缩增加了通用活性。对氨基苯汞乙酸(APMA)处理增加了压缩诱导的MMPs的通用活性。