Differential effects of local application of BMP-2 or TGF-β1 on both articular cartilage composition and osteophyte formation

被引:239
作者
van Beuningen, HM [1 ]
Glansbeek, HL [1 ]
van der Kraan, PM [1 ]
van den Berg, WB [1 ]
机构
[1] Univ Nijmegen Hosp, Dept Rheumatol, NL-6525 GA Nijmegen, Netherlands
关键词
BMP-2; TGF-beta; 1; proteoglycan; osteophytes;
D O I
10.1053/joca.1998.0129
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: The related molecules bone morphogenetic protein-2 (BMP-2) and transforming growth factor beta-1 (TGF-beta 1) have both been shown to stimulate chondrocyte proteoglycan (PG) synthesis in vitro. We investigated the in-vivo effects of these factors on articular cartilage PG metabolism. Design: Several doses of BMP-2 or TGF-beta 1 were injected into the murine knee joint, once or repeatedly. Patellar cartilage PG synthesis it-as measured by [S-35]-sulfate incorporation and reverse transcriptase polymerase chain reaction (RT-PCR). PG content was analyzed by measuring safranin O staining intensity on histologic sections. Results: A single injection of 200 ng BMP-X induced a much earlier and more impressive stimulation of articular cartilage PG synthesis, than 200 ng TGF-beta 1. RT-PCR revealed that both factors upregulated mRNA of aggrecan more than that of biglycan and decorin. However, 21 days after a single injection of 200 ng TGF-beta 1 PG synthesis still was significantly increased, while stimulation by BMP-2 only lasted for 3 to ii days. Stimulation by BMP-2 could be prolonged to at least 2 weeks by triple injections of 200 ng each, at alternate days. Remarkably, even after this intense exposure to BMP-2, stimulation of PG synthesis was not reflected in long-lasting enhancement of PG content of articular cartilage. In contrast, even a single injection with 200 ng of TGF-beta 1 induced prolonged enhancement of PCT content. After repeated injections, both BMP-2 and TGF-beta 1 induced chondrogenesis at specific sites. 'Chondrophytes' induced by BMP-2 were found predominantly in the region where the growth plates meet the joint space, while those triggered by TGF-beta 1 originated from the periosteum also at sites remote from the growth plates. Conclusions: BMP-2 and TGF-beta stimulate PG synthesis and PG content with differ ent kinetics, and these factors have different chondro-inductive properties.
引用
收藏
页码:306 / 317
页数:12
相关论文
共 41 条
[1]   Transforming growth factor beta and bone morphogenetic protein 2 for bone ingrowth: A comparison using bone chambers in rats [J].
Aspenberg, P ;
Jeppsson, C ;
Wang, JS ;
Bostrom, M .
BONE, 1996, 19 (05) :499-503
[2]  
ASUNDI VK, 1992, EUR J CELL BIOL, V59, P314
[3]   TRANSFORMING GROWTH FACTOR-B REGULATES PRODUCTION OF PROTEOGLYCANS BY MESANGIAL CELLS [J].
BORDER, WA ;
OKUDA, S ;
LANGUINO, LR ;
RUOSLAHTI, E .
KIDNEY INTERNATIONAL, 1990, 37 (02) :689-695
[4]   TRANSFORMING GROWTH FACTOR-BETA IS A POTENT INHIBITOR OF IL-1 INDUCED PROTEASE ACTIVITY AND CARTILAGE PROTEOGLYCAN DEGRADATION [J].
CHANDRASEKHAR, S ;
HARVEY, AK .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 157 (03) :1352-1359
[5]   Recombinant human osteogenic protein 1 is a potent stimulator of the synthesis of cartilage proteoglycans and collagens by human articular chondrocytes [J].
Flechtenmacher, J ;
Huch, K ;
Thonar, EJMA ;
Mollenhauer, JA ;
Davies, SR ;
Schmid, TM ;
Puhl, W ;
Sampath, TK ;
Aydelotte, MB ;
Kuettner, KE .
ARTHRITIS AND RHEUMATISM, 1996, 39 (11) :1896-1904
[6]   VERSICAN GENE-EXPRESSION IN HUMAN ARTICULAR-CARTILAGE AND COMPARISON OF MESSENGER-RNA SPLICING VARIATION WITH AGGRECAN [J].
GROVER, J ;
ROUGHLEY, PJ .
BIOCHEMICAL JOURNAL, 1993, 291 :361-367
[7]   TRANSFORMING GROWTH-FACTOR-BETA-1 REGULATES TISSUE INHIBITOR OF METALLOPROTEINASES-1 EXPRESSION IN DIFFERENTIATED HUMAN ARTICULAR CHONDROCYTES [J].
GUNTHER, M ;
HAUBECK, HD ;
VANDELEUR, E ;
BLASER, J ;
BENDER, S ;
GUTGEMANN, I ;
FISCHER, DC ;
TSCHESCHE, H ;
GREILING, H ;
HEINRICH, PC ;
GRAEVE, L .
ARTHRITIS AND RHEUMATISM, 1994, 37 (03) :395-405
[8]  
KAHARI VM, 1991, J BIOL CHEM, V266, P10608
[9]  
KAWAGUCHI H, 1992, SPINE, V17, pS33
[10]   THE TGF-BETA SUPERFAMILY - NEW MEMBERS, NEW RECEPTORS, AND NEW GENETIC TESTS OF FUNCTION IN DIFFERENT ORGANISMS [J].
KINGSLEY, DM .
GENES & DEVELOPMENT, 1994, 8 (02) :133-146