Yeh L A, Augustine A J, Lee P, Riviere L R, Sheldon A
Department of Enzyme Biochemistry, OsteoArthritis Sciences, Inc., Cambridge, MA 02139, USA.
J Rheumatol. 1995 Sep;22(9):1740-6.
To determine the ability of interleukin-4 (IL-4) to inhibit the degradation of proteoglycan in bovine articular cartilage explants stimulated by human interleukin-1 (IL-1 alpha), tumor necrosis factor (TNF-alpha), a combination of TNF-alpha and IL-1 alpha, and lipopolysaccharide (LPS).
35SO4 radiolabelled bovine radiocarpal cartilage explants were treated with IL-1 alpha, TNF-alpha, TNF-alpha plus IL-1 alpha, or LPS, plus various concentrations of IL-4 for 72 h. Proteoglycan released to the media was analyzed by scintillation counting and composite gel electrophoresis. Media samples were also analyzed by Western immunoblotting for metalloproteinases and TIMP.
IL-4 significantly reduced the cartilage proteoglycan degradation induced by IL-1 alpha, TNF-alpha, TNF-alpha plus IL-1 alpha, or LPS (50% inhibitory concentration, IC50 for IL-4 ranged from about 15 to 50 ng/ml). Western blotting showed that media stromelysin levels were increased by IL-1 alpha, TNF-alpha, and LPS, but that IL-4 had no observable effect. Composite gel electrophoresis demonstrated quantitative and qualitative differences in proteoglycan degradation after IL-4 treatment.
IL-4 has a potent inhibitory effect on cartilage degradation after stimulation with IL-1 alpha, TNF-alpha, TNF-alpha plus IL-1 alpha, or LPS. These results suggest that IL-4 should be investigated further for therapeutic value as a chondroprotective agent for the treatment of arthritis.
确定白细胞介素-4(IL-4)抑制人白细胞介素-1(IL-1α)、肿瘤坏死因子(TNF-α)、TNF-α与IL-1α联合以及脂多糖(LPS)刺激的牛关节软骨外植体中蛋白聚糖降解的能力。
用IL-1α、TNF-α、TNF-α加IL-1α或LPS,以及不同浓度的IL-4处理35SO4放射性标记的牛桡腕关节软骨外植体72小时。通过闪烁计数和复合凝胶电泳分析释放到培养基中的蛋白聚糖。还通过蛋白质免疫印迹法对培养基样本进行金属蛋白酶和金属蛋白酶组织抑制剂(TIMP)分析。
IL-4显著降低了由IL-1α、TNF-α、TNF-α加IL-1α或LPS诱导的软骨蛋白聚糖降解(IL-4的50%抑制浓度,IC50范围约为15至50 ng/ml)。蛋白质印迹显示,IL-1α、TNF-α和LPS可使培养基中基质溶解素水平升高,但IL-4未观察到明显作用。复合凝胶电泳显示IL-4处理后蛋白聚糖降解存在定量和定性差异。
IL-4对IL-1α、TNF-α、TNF-α加IL-1α或LPS刺激后的软骨降解具有强大的抑制作用。这些结果表明,作为一种治疗关节炎的软骨保护剂,IL-4的治疗价值应进一步研究。