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Differential expression of mRNAs for endopeptidases in phenotypically modulated (`dedifferentiated') human articular chondrocytes

机译:表型调节(“去分化”)人关节软骨细胞中内肽酶mRNA的差异表达

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>Human articular chondrocytes modulated away from their original phenotype by serial subcultures in monolayer differentially express mRNAs for endopeptidases. The mRNAs for the cathepsins B and L are extremely low in differentiated cells, but are soon expressed in parallel with the loss of the differentiated state. In contrast, the mRNA for collagenase-1 is strongly expressed by differentiated chondrocytes and declines rapidly following phenotypic modulation. The mRNA for stromelysin-1 and the tissue inhibitor of metalloproteinases-2 is high and does not appreciably change after modulation. Chondrocyte activation induced by alteration of its original phenotype leads to the expression of endopeptidases in a way that markedly differs from that induced by cytokines. The results are relevant to cartilage catabolism in osteoarthritis and suggest a prominent role of fibroblastic metaplasia on the part of the chondrocytes as a mechanism of expressing catabolic endopeptidases.
机译:在单层中,通过连续继代培养,人类关节软骨细胞从其原始表型中被调制出来,从而差异表达内肽酶。组织蛋白酶B和L的mRNA在分化的细胞中极低,但是很快与分化状态的丧失并行地表达。相反,胶原酶-1的mRNA在分化的软骨细胞中强烈表达,并在表型调节后迅速下降。基质溶素-1和金属蛋白酶-2的组织抑制剂的mRNA高,在调节后没有明显变化。通过改变其原始表型诱导的软骨细胞活化导致内肽酶的表达与细胞因子诱导的表达明显不同。该结果与骨关节炎中的软骨分解代谢有关,并提示成纤维细胞化生在软骨细胞的一部分上作为表达分解代谢内肽酶的机制的重要作用。

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