Tang Yue-qiong, Shan Zheng-zheng, Dai Sheng-ming
Department of Rheumatology & Immunology, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
Zhonghua Yi Xue Za Zhi. 2008 Jun 3;88(21):1493-7.
To study the expression level of caveolin-1 in articular chondrocytes in patients with osteoarthritis (OA), and whether catabolic factor IL-1beta stimulate caveolin-1 expression in articular chondrocytes.
In human OA cartilage, caveolin-1 mRNA was investigated by quantitative real-time RT-PCR while caveolin-1 protein was detected by immunohistologic analysis in 8 cases. OA model was prepared by unilateral anterior cruciate ligament and medial collateral ligament transection in 20 rats. In cultured OA chondrocytes, caveolin-1 mRNA expression was studied by RT-PCR and quantitative real-time RT-PCR, and caveolin-1 protein was analyzed by Western blotting.
In 6 of 8 OA cases, human OA articular cartilage, higher expression levels of both caveolin-1 mRNA and caveolin-1 protein were found in advanced degenerated cartilage than less degenerated cartilage of the same joints. In rat OA model, upregulated caveolin-1 expression was found, which was associated with the degree of cartilage destruction. IL-1beta (10 ng/ml) upregulated caveolin-1 mRNA/protein expression in cultured OA chondrocytes for at least 48 hours.
Enhanced expression level of caveolin-1 is associated with cartilage degeneration in OA. IL-1beta stimulates caveolin-1 expression in articular chondrocytes, which may be responsible for OA development.
研究骨关节炎(OA)患者关节软骨细胞中小窝蛋白-1(caveolin-1)的表达水平,以及分解代谢因子白细胞介素-1β(IL-1β)是否刺激关节软骨细胞中caveolin-1的表达。
在8例人类OA软骨中,通过定量实时逆转录聚合酶链反应(RT-PCR)研究caveolin-1 mRNA,同时通过免疫组织学分析检测caveolin-1蛋白。通过切断20只大鼠的单侧前交叉韧带和内侧副韧带制备OA模型。在培养的OA软骨细胞中,通过RT-PCR和定量实时RT-PCR研究caveolin-1 mRNA表达,并通过蛋白质印迹法分析caveolin-1蛋白。
在8例OA病例中的6例中,人类OA关节软骨中,与同一关节退变较轻的软骨相比,退变严重的软骨中caveolin-1 mRNA和caveolin-1蛋白的表达水平更高。在大鼠OA模型中,发现caveolin-1表达上调,这与软骨破坏程度相关。IL-1β(10 ng/ml)在培养的OA软骨细胞中至少48小时上调caveolin-1 mRNA/蛋白表达。
caveolin-1表达水平增强与OA中的软骨退变相关。IL-1β刺激关节软骨细胞中caveolin-1的表达,这可能是OA发展的原因。