Westacott C I, Atkins R M, Dieppe P A, Elson C J
Department of Pathology, University of Bristol, UK.
J Rheumatol. 1994 Sep;21(9):1710-5.
To determine whether the previously observed enhanced susceptibility of osteoarthritic (OA) cartilage to tumor necrosis factor-alpha (TNF-alpha) induced degradation could be due to differences in receptor expression.
Using specific monoclonal antibodies flow cytometry was used to identify and quantify 2 TNF-alpha receptors on the surface of chondrocytes isolated from human articular cartilage.
The proportion of chondrocytes expressing p55 TNF-alpha receptor was significantly higher in populations from OA cartilage (p < 0.01) when compared with similar populations from non-arthritic cartilage. The number of p55 receptors/chondrocyte was also significantly higher (p < 0.01) in OA. A significant correlation (r = 0.72, p < 0.18) was found in OA between the numbers of chondrocytes expressing p75 receptor and the number of receptors/chondrocyte.
p55 TNF-alpha receptor expression is significantly increased on OA chondrocytes ex vivo. Enhanced expression of p55, purported to be the biologically active receptor, could contribute to OA cartilage degradation.
确定先前观察到的骨关节炎(OA)软骨对肿瘤坏死因子-α(TNF-α)诱导降解的易感性增强是否可能归因于受体表达的差异。
使用特异性单克隆抗体,通过流式细胞术鉴定和定量从人关节软骨分离的软骨细胞表面的两种TNF-α受体。
与非关节炎软骨的相似细胞群体相比,OA软骨细胞群体中表达p55 TNF-α受体的软骨细胞比例显著更高(p < 0.01)。OA中每个软骨细胞的p55受体数量也显著更高(p < 0.01)。在OA中,表达p75受体的软骨细胞数量与每个软骨细胞的受体数量之间存在显著相关性(r = 0.72,p < 0.18)。
离体OA软骨细胞上p55 TNF-α受体表达显著增加。据称具有生物活性的p55受体表达增强可能导致OA软骨降解。