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Measurement of cartilage oligomeric matrix protein (COMP) in normal and diseased equine synovial fluids.

机译:正常和患病马滑液中软骨寡聚基质蛋白(COMP)的测量。

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OBJECTIVE: This study was designed to assay cartilage oligomeric matrix protein (COMP) in equine synovial fluids and to compare the concentration in synovial fluids from normal horses with joint diseased horses. The relationship between the COMP degradation and the matrix metalloproteinase activity in synovial fluids was also investigated. DESIGN: Using COMP antigen prepared from equine articular cartilage and murine monoclonal antibody (12C4) raised against human COMP, an inhibition ELISA was developed. COMP in equine synovial fluids from normal and diseased joints was quantified. Metalloproteinase activities were evaluated in the same synovial fluids by a gelatin degradation ELISA. COMP fragments were evaluated qualitatively by Western blotting. RESULTS: The COMP inhibition ELISA was reliable at concentrations of equine COMP between 62.5 and 2000 ng/ml. COMP values in joint fluids in both aseptic and septic joint disease (19.7+/-15.3 and 16.1+/-11.2 microg/ml, respectively) were significantly (P < 0.001) lower than normal (53.2+/-29.0 microg/ml). The molecular sizes of COMP on immunoblots were different between normal and diseased synovial fluids; more fragments were seen in diseased fluids. The aseptic (26.6 +/- 20.6%) and septic joint disease synovial fluids (36.1 +/- 37.5%) had significantly higher (P < 0.02 and 0.002, respectively) gelatinolytic activities than normal (13.6 +/- 13.7%). There was a negative correlation (R = -0.31, P < 0.002) between COMP level and gelatinase activity.Conclusions We conclude that the fragment pattern and the absolute COMP concentration maybe useful for monitoring joint disease, and that COMP degradation in synovial fluids from progressed joint disease may be due to MMP gelatinolytic activity. Copyright 2001
机译:目的:本研究旨在分析马滑液中的软骨寡聚基质蛋白(COMP),并比较正常马和关节病马的滑液中的软骨浓度。还研究了滑膜液中COMP降解与基质金属蛋白酶活性之间的关系。设计:使用由马关节软骨和针对人类COMP的鼠单克隆抗体(12C4)制备的COMP抗原,开发了抑制ELISA。定量来自正常和患病关节的马滑液中的COMP。通过明胶降解ELISA评估相同滑液中的金属蛋白酶活性。通过蛋白质印迹对COMP片段进行定性评估。结果:当马COMP浓度在62.5至2000 ng / ml之间时,COMP抑制ELISA是可靠的。无菌和败血性关节疾病的关节液中COMP值(分别为19.7 +/- 15.3和16.1 +/- 11.2 microg / ml)显着(P <0.001)低于正常值(53.2 +/- 29.0 microg / ml) 。在正常和患病的滑液之间,免疫印迹上COMP的分子大小是不同的。在患病的液体​​中发现了更多碎片。无菌(26.6 +/- 20.6%)和败血症性关节疾病滑液(36.1 +/- 37.5%)的明胶分解活性明显高于正常(13.6 +/- 13.7%)(分别为P <0.02和0.002)。结论:COMP水平与明胶酶活性之间呈负相关(R = -0.31,P <0.002)。结论我们得出结论,碎片模式和COMP绝对浓度可能有助于监测关节疾病,滑膜液中COMP的降解随疾病进展而发展。关节疾病可能是由于MMP的明胶分解活性所致。版权所有2001

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