Patterson Angela M, Siddall Hilary, Chamberlain Giselle, Gardner Lucy, Middleton Jim
Centre for Science and Technology in Medicine, Keele University at Robert Jones and Agnes Hunt Orthopaedic Hospital, Oswestry, UK.
J Pathol. 2002 May;197(1):108-16. doi: 10.1002/path.1100.
The expression of chemokine binding sites on the endothelial cells of venules in inflamed synovia was examined and whether the Duffy antigen/receptor for chemokines (DARC) was involved. In situ binding assays were performed to determine the expression of chemokine binding sites from rheumatoid (n = 10) and non-rheumatoid (n = 10) synovia. The expression of DARC protein and mRNA was examined by immunohistochemistry and northern blotting. The involvement of DARC in chemokine binding was studied by incubating sections with blocking antibodies to DARC (Fy3 and 6), to find out if these reduced 125I-IL-8 binding. Binding of radiolabelled chemokines IL-8, RANTES, MCP-1, but not MIP-1alpha, was found on venular endothelial cells in inflamed synovia from both rheumatoid and non-rheumatoid patients. Excess homologous unlabelled chemokine displaced binding and excess unlabelled RANTES could displace radiolabelled IL-8 binding. DARC protein expression was demonstrated on venular endothelial cells in all samples and DARC mRNA could be detected in extracts from synovia. There was downregulation of DARC protein and mRNA in rheumatoid samples. Binding of IL-8 to both rheumatoid and non-rheumatoid synovia was significantly reduced in the presence of anti-DARC Fy3 and Fy6 monoclonal antibodies. These findings show the expression of a multispecific chemokine binding site on the inflamed synovial endothelium, with evidence for involvement of DARC. This suggests a potential role for DARC in the inflammatory processes involved in synovitis.
研究了炎症滑膜中小静脉内皮细胞趋化因子结合位点的表达情况,以及趋化因子Duffy抗原/受体(DARC)是否参与其中。进行原位结合试验以确定类风湿性(n = 10)和非类风湿性(n = 10)滑膜中趋化因子结合位点的表达。通过免疫组织化学和Northern印迹法检测DARC蛋白和mRNA的表达。通过用针对DARC的阻断抗体(Fy3和6)孵育切片来研究DARC在趋化因子结合中的作用,以确定这些抗体是否能减少125I-IL-8的结合。在类风湿性和非类风湿性患者炎症滑膜的小静脉内皮细胞上发现了放射性标记的趋化因子IL-8、RANTES、MCP-1(但不是MIP-1α)的结合。过量的同源未标记趋化因子可取代结合,过量的未标记RANTES可取代放射性标记的IL-8结合。在所有样本的小静脉内皮细胞上均证实有DARC蛋白表达,并且在滑膜提取物中可检测到DARC mRNA。类风湿性样本中DARC蛋白和mRNA表达下调。在存在抗DARC Fy3和Fy6单克隆抗体的情况下,IL-8与类风湿性和非类风湿性滑膜的结合均显著减少。这些发现表明炎症滑膜内皮细胞上存在多特异性趋化因子结合位点,并有证据表明DARC参与其中。这提示DARC在滑膜炎相关炎症过程中可能发挥作用。