首页> 美国卫生研究院文献>Annals of the Rheumatic Diseases >Characterisation of the cell type-specificity of collagenase 3 mRNA expression in comparison with membrane type 1 matrix metalloproteinase and gelatinase A in the synovial membrane in rheumatoid arthritis
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Characterisation of the cell type-specificity of collagenase 3 mRNA expression in comparison with membrane type 1 matrix metalloproteinase and gelatinase A in the synovial membrane in rheumatoid arthritis

机译:类风湿关节炎滑膜中胶原酶3 mRNA表达的细胞类型特异性与膜型1基质金属蛋白酶和明胶酶A的比较

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摘要

Objective: To study the pattern and cell type-specificity of collagenase 3, membrane-type 1 matrix metalloproteinase (MT1-MMP), and gelatinase A mRNA expression in the synovial membrane in rheumatoid arthritis (RA). Methods: The mRNA expression of collagenase 3, MT1-MMP, and gelatinase A was characterised by northern blot analysis, reverse transcriptase-polymerase chain reaction, and in situ hybridisation. In situ hybridisation was performed in combination with the immunohistochemical detection of cell type-specific antigens. Results: Synovial membrane specimens from 19 of 21 patients with RA expressing collagenase 3 mRNA were positive for MT1-MMP and gelatinase A mRNA. In control samples from patients without destructive inflammatory joint diseases collagenase 3 mRNA was not expressed and only in two of seven cases was a coexpression of MT1-MMP and gelatinase A mRNA detected. Fibroblast-like cells of the synovial membrane were found to be the predominant source of collagenase 3, MT1-MMP, and gelatinase A mRNA expression in lining and sublining layers as well as at the synovial membrane-cartilage interface. Additionally, the expression of MT1-MMP mRNA was detected in endothelial cells. Collagenase 3 mRNA expression was found in about 5% of CD68 positive macrophages. Conclusions: Collagenase 3 mRNA is expressed simultaneously with MT1-MMP and gelatinase A mRNA in fibroblast-like cells of the synovial membrane in RA. These results suggest (a) a broad extracellular proteolytic potential of fibroblast-like cells and (b) an important role of cell surface associated procollagenase 3 activation by MT1-MMP and gelatinase A for cartilage degradation by invading fibroblast-like cells.
机译:目的:研究类风湿关节炎(RA)滑膜中胶原酶3,膜1型基质金属蛋白酶(MT1-MMP)和明胶酶A mRNA表达的模式和细胞类型特异性。方法:通过RNA印迹分析,逆转录酶-聚合酶链反应和原位杂交的方法对胶原酶3,MT1-MMP和明胶酶A的mRNA表达进行表征。结合细胞类型特异性抗原的免疫组织化学检测进行原位杂交。结果:21例RA患者中19例表达胶原酶3 mRNA的滑膜标本MT1-MMP和明胶酶A mRNA阳性。在没有破坏性炎性关节疾病的患者的对照样品中,胶原酶3 mRNA不表达,只有七分之二的患者检测到MT1-MMP和明胶酶A mRNA的共表达。发现滑膜的成纤维样细胞是胶原酶3,MT1-MMP和明胶酶A mRNA在衬层和衬层以及滑膜-软骨界面的主要表达来源。另外,在内皮细胞中检测到MT1-MMP mRNA的表达。在约68%的CD68阳性巨噬细胞中发现胶原酶3mRNA表达。结论:RA大鼠滑膜成纤维样细胞中胶原酶3 mRNA与MT1-MMP和明胶酶A mRNA同时表达。这些结果表明(a)成纤维细胞样细胞具有广泛的细胞外蛋白水解潜能,并且(b)MT1-MMP和明胶酶A激活的细胞表面相关的胶原蛋白3活化对于侵袭成纤维细胞样细胞的软骨降解具有重要作用。

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