Tchetverikov I, Lohmander L S, Verzijl N, Huizinga T W J, TeKoppele J M, Hanemaaijer R, DeGroot J
Division of Biomedical Research, TNO Prevention and Health, PO Box 2215, 2301 CE, Leiden, Netherlands.
Ann Rheum Dis. 2005 May;64(5):694-8. doi: 10.1136/ard.2004.022434.
To determine protein and activity levels of matrix metalloproteinases 1 and 3 (MMP-1 and MMP-3) in synovial fluid of patients with knee joint injury, primary osteoarthritis, and acute pyrophosphate arthritis (pseudogout).
Measurements were done on knee synovial fluid obtained in a cross sectional study of cases of injury (n = 283), osteoarthritis (n = 105), and pseudogout (n = 65), and in healthy controls (n = 35). Activity of MMP-1 and MMP-3 in alpha(2) macroglobulin complexes was measured using specific low molecular weight fluorogenic substrates. ProMMP-1, proMMP-3, and TIMP-1 (tissue inhibitor of metalloproteinase 1) were quantified by immunoassay.
Mean levels of proMMP-1, proMMP-3, and TIMP-1 were increased in injury, osteoarthritis, and pseudogout compared with controls. MMP-1 activity was increased in pseudogout and injury groups over control levels, whereas MMP-3 activity was increased only in the pseudogout group. The increase in MMP-1 activity coincided with a decrease in TIMP-1 levels in the injury group.
Patients with joint injury have a persistent increase in proMMP-1 and proMMP-3 in synovial fluid and an increase in activated MMPs, which are not inhibited by TIMP. The differences in activation and inhibition patterns between the study groups are consistent with disease specific patterns of MMP activation and/or inhibition in joint pathology.
测定膝关节损伤、原发性骨关节炎及急性焦磷酸关节炎(假性痛风)患者滑液中基质金属蛋白酶1和3(MMP - 1和MMP - 3)的蛋白及活性水平。
对在一项横断面研究中获取的膝关节滑液进行检测,该研究包括损伤病例(n = 283)、骨关节炎病例(n = 105)、假性痛风病例(n = 65)以及健康对照者(n = 35)。使用特定的低分子量荧光底物测定α2巨球蛋白复合物中MMP - 1和MMP - 3的活性。通过免疫测定法对前MMP - 1、前MMP - 3和金属蛋白酶组织抑制剂1(TIMP - 1)进行定量分析。
与对照组相比,损伤、骨关节炎和假性痛风患者的前MMP - 1、前MMP - 3和TIMP - 1平均水平均升高。假性痛风组和损伤组的MMP - 1活性高于对照组水平,而MMP - 3活性仅在假性痛风组升高。损伤组中MMP - 1活性的增加与TIMP - 1水平的降低同时出现。
关节损伤患者滑液中的前MMP - 1和前MMP - 3持续增加,且活化的MMPs增加,而TIMP不能抑制这些增加。研究组之间活化和抑制模式的差异与关节病理中MMP活化和/或抑制的疾病特异性模式一致。