The new collagenase, collagenase-3, is expressed and synthesized by human chondrocytes but not by synoviocytes - A role in osteoarthritis

被引:415
作者
Reboul, P [1 ]
Pelletier, JP [1 ]
Tardif, G [1 ]
Cloutier, JM [1 ]
MartelPelletier, J [1 ]
机构
[1] UNIV MONTREAL,NOTRE DAME HOSP,LC SIMARD RES CTR,RHEUMATOL OSTEOARTHRIT RES UNIT,MONTREAL,PQ H2L 4K8,CANADA
关键词
cartilage; collagen; chondrocytes; arthritis; cytokines;
D O I
10.1172/JCI118636
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Recently, a new human collagenase, collagenase-3 has been identified. Since collagen changes are of particular importance in cartilage degeneration, we investigated if collagenase-3 plays a role in osteoarthritis (OA). Reverse transcriptase-PCR analysis revealed that in articular tissues collagenase-3 was expressed by the chondrocytes but not by the synoviocytes. Northern blot analysis of the chondrocyte mRNA revealed the presence of two major gene transcripts of 3.0 and 2.5 kb, and a third one of 2.2 kb was occasionally present. Compared to normal, OA showed a significantly higher (3.0 kb, P less than or equal to 0.05; 2.5 kb, P less than or equal to 0.03) level of collagenase-3 mRNA expression. Collagenase-3 had a higher catalytic velocity rate (about fivefold) than collagenase-1 on type II collagen. With the use of two specific antibodies, we showed that human chondrocytes had the ability to produce collagenase-3 as a proenzyme and as a glycosylated doublet. The chondrocyte collagenase-3 protein is produced in a significantly higher (P less than or equal to 0.04) level in OA (similar to 9.5-fold) than in normal. The synthesis and expression of this new collagenase could also be modulated by two proinflammatory cytokines, IL-1 beta and TNF-alpha, in a time- and dose-dependent manner. This study provides novel and interesting data on collagenase-3 expression and synthesis in human cartilage cells and suggest its involvement in human OA cartilage pathophysiology.
引用
收藏
页码:2011 / 2019
页数:9
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