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类风湿关节炎中基质降解的机制。

Mechanisms of matrix degradation in rheumatoid arthritis.

作者信息

Krane S M, Conca W, Stephenson M L, Amento E P, Goldring M B

机构信息

Department of Medicine, Harvard Medical School, Boston, Massachusetts.

出版信息

Ann N Y Acad Sci. 1990;580:340-54. doi: 10.1111/j.1749-6632.1990.tb17943.x.

Abstract

In the inflammatory synovium production of collagenase is probably responsible for the degradation of collagen in the extracellular matrix and distortion of the architecture and function of the joints. Major collagenase-producing cells are mesenchymal cells such as fibroblasts and chondrocytes, which synthesize and secrete the enzyme influenced by the action of cytokines produced by adjacent mononuclear cells. The cytokines act primarily through cell-surface receptors, whose signal is probably then mediated by complexes of nuclear oncoproteins, to activate transcription of the procollagenase gene. The increased production of collagenase ultimately is the result of a cascade of cellular effects involving complex interactions of different ligands in a system characterized by amplification and feedback loops.

摘要

在炎性滑膜中,胶原酶的产生可能是细胞外基质中胶原蛋白降解以及关节结构和功能变形的原因。主要产生胶原酶的细胞是间充质细胞,如成纤维细胞和软骨细胞,它们在相邻单核细胞产生的细胞因子作用下合成并分泌这种酶。细胞因子主要通过细胞表面受体起作用,其信号可能随后由核癌蛋白复合物介导,以激活前胶原酶基因的转录。胶原酶产生的增加最终是一系列细胞效应的结果,这些效应涉及一个以放大和反馈环为特征的系统中不同配体的复杂相互作用。

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