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Differential expression of mRNAs for endopeptidases in phenotypically modulated ('dedifferentiated') human articular chondrocytes
被引:16
作者:
Kostoulas, G
Lang, A
Trueb, B
Baici, A
机构:
[1] UNIV ZURICH HOSP,DEPT RHEUMATOL,CH-8091 ZURICH,SWITZERLAND
[2] UNIV BERN,ME MULLER INST BIOMECH,CH-3010 BERN,SWITZERLAND
关键词:
cathepsin B;
cathepsin L;
collagenase-1;
stromelysin-1;
TIMP-2;
osteoarthritis;
D O I:
10.1016/S0014-5793(97)00825-9
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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 was 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. (C) 1997 Federation of European Biochemical Societies.
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页码:453 / 455
页数:3
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