TRANSFORMING GROWTH-FACTOR-BETA-1 REGULATES TISSUE INHIBITOR OF METALLOPROTEINASES-1 EXPRESSION IN DIFFERENTIATED HUMAN ARTICULAR CHONDROCYTES

被引:96
作者
GUNTHER, M
HAUBECK, HD
VANDELEUR, E
BLASER, J
BENDER, S
GUTGEMANN, I
FISCHER, DC
TSCHESCHE, H
GREILING, H
HEINRICH, PC
GRAEVE, L
机构
[1] RHEIN WESTFAL TH AACHEN,INST BIOCHEM,AACHEN,GERMANY
[2] RHEIN WESTFAL TH AACHEN,INST KLIN CHEM & PATHOBIOCHEM,AACHEN,GERMANY
[3] UNIV BIELEFELD,INST BIOCHEM,BIELEFELD,GERMANY
来源
ARTHRITIS AND RHEUMATISM | 1994年 / 37卷 / 03期
关键词
D O I
10.1002/art.1780370314
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To investigate the role of interleukin-6 (IL-6) and transforming growth factor beta 1 (TGF beta 1) in the regulation of tissue inhibitor of metalloproteinases-1 (TIMP-1) synthesis in human articular chondrocytes. Methods. Articular cartilage was obtained from human knee joints 24 hours after death. Chondrocytes were isolated by collagenase digestion and embedded in low-gelling-temperature agarose. After stimulation by cytokines, total RNA was isolated and analyzed by Northern blotting. TIMP-1 protein levels were determined using a competitive enzyme-linked immunosorbent assay. Results. Human chondrocytes in agarose culture expressed messenger RNA (mRNA) for the IL-6 receptor (gp80) and its signal-transducing subunit gp130. In contrast to the findings in a previous study, IL-6 did not stimulate TIMP-1 expression in these cells, whereas TGF beta 1 was an important inducer of TIMP-1 mRNA and protein synthesis. Conclusion. Our findings suggest that TGF beta 1 has a protective effect on the extracellular matrix of human articular chondrocytes.
引用
收藏
页码:395 / 405
页数:11
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