TREATMENT OF PROTEOGLYCAN AGGREGATES WITH PHYSEAL ENZYMES REDUCES THEIR ABILITY TO INHIBIT HYDROXYAPATITE PROLIFERATION IN A GELATIN GEL

被引:27
作者
BOSKEY, AL
MARESCA, M
ARMSTRONG, AL
EHRLICH, MG
机构
[1] CORNELL UNIV, MED CTR, COLL MED, DEPT BIOCHEM, NEW YORK, NY 10021 USA
[2] BROWN UNIV, PROVIDENCE, RI 02912 USA
[3] RHODE ISL HOSP, DEPT ORTHOPED, PROVIDENCE, RI 02902 USA
关键词
CALCIFICATION; GROWTH PLATE; HYDROXYAPATITE; PROTEOGLYCANASE; PROTEOGLYCAN;
D O I
10.1002/jor.1100100302
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
In vitro, cartilage proteoglycans (PGs) are effective inhibitors of hydroxyapatite formation and growth. Their inhibitory ability decreases with decreasing PG size and charge density. It has been suggested that the enzyme-mediated alteration in the size and conformation of PGs in the growth plate may similarly facilitate the calcification process. In this study, a gelatin gel system was used to monitor hydroxyapatite formation and growth in the presence of proteoglycan aggregates, before and after enzyme treatment. To reproduce the physeal degradation cascade, an enzyme preparation was used that contained all of the growth plate enzymes. At a concentration of 500-mu-g/ml, the untreated proteoglycan aggregates reduced the amount of mineral formed by 30%. When the aggregates were treated with the heat-inactivated enzyme, the same extent of inhibition was found. In contrast, treating the aggregates with the crude growth plate enzyme preparation removed all the inhibitory ability, such that 500-mu-g/ml of proteoglycan preparation yielded 10% more mineral than the controls. Treatment of the aggregates with chondroitinase ABC and trypsin, similarly removed all the inhibitory ability. These data, suggest that enzymatic degradation of proteoglycans may contribute to the regulation of growth plate calcification.
引用
收藏
页码:313 / 319
页数:7
相关论文
共 49 条
[41]  
POOLE AR, 1989, ANAT REC, V224, P167
[42]  
Rosenberg L, 1975, DYNAMICS CONNECTIVE, P105
[43]   DEGRADATION OF CARTILAGE PROTEOGLYCANS BY TISSUE PROTEINASES - PROTEOGLYCAN STRUCTURE AND ITS SUSCEPTIBILITY TO PROTEOLYSIS [J].
ROUGHLEY, PJ ;
BARRETT, AJ .
BIOCHEMICAL JOURNAL, 1977, 167 (03) :629-637
[44]  
RUOSLAHTI E, 1988, ANNU REV CELL BIOL, V4, P229, DOI 10.1146/annurev.cb.04.110188.001305
[45]   NEUTRAL PROTEASES AND CATHEPSIN D IN HUMAN ARTICULAR CARTILAGE [J].
SAPOLSKY, AI ;
HOWELL, DS ;
WOESSNER, JF .
JOURNAL OF CLINICAL INVESTIGATION, 1974, 53 (04) :1044-1055
[46]  
SAPOLSKY AI, 1982, ARTHRITIS RHEUM, V25, P871
[47]   ULTRASTRUCTURAL MODIFICATIONS OF PROTEOGLYCANS COINCIDENT WITH MINERALIZATION IN LOCAL REGIONS OF RAT GROWTH PLATE [J].
SHEPARD, N ;
MITCHELL, N .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1985, 67A (03) :455-464
[48]   THE DETERMINATION OF METALS IN BLOOD SERUM BY ATOMIC ABSORPTION SPECTROSCOPY .1. CALCIUM [J].
WILLIS, JB .
SPECTROCHIMICA ACTA, 1960, 16 (03) :259-&
[49]  
WOESSNER JF, 1987, J RHEUMATOL, V14, P36