Growth Factor Regulation of Growth Factors in Articular Chondrocytes

被引:44
作者
Shi, Shuiliang [1 ]
Mercer, Scott [1 ]
Eckert, George J. [2 ]
Trippel, Stephen B. [1 ,3 ]
机构
[1] Indiana Univ, Sch Med, Dept Orthopaed Surg, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Med, Div Biostat, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Anat & Cell Biol, Indianapolis, IN 46202 USA
关键词
DEFECTS IN-VIVO; FACTOR-BETA; IGF-I; PROTEOGLYCAN SYNTHESIS; OSTEOGENIC PROTEIN-1; CARTILAGE EXPLANTS; ENHANCED REPAIR; TGF-BETA; METABOLISM; COLLAGEN;
D O I
10.1074/jbc.M807859200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Several lines of evidence indicate that polypeptide growth factors are important in articular cartilage homeostasis and repair. It is not yet clear how these growth factors are regulated. We tested the hypothesis that the growth factors responsible for regulating cartilage are themselves regulated by growth factors. We delivered insulin-like growth factor I (IGF-I), fibroblast growth factor-2 (FGF-2), and/or transforming growth factor-beta 1 (TGF-beta 1) to adult bovine articular chondrocytes in primary culture and measured the resulting changes in IGF-I, FGF-2, and TGF-beta 1 gene expression and protein production. These growth factors differentially regulated their own and each others gene expression and protein production. In concert, they regulated each other in an interactive fashion. Their interactions ranged from inhibitory to synergistic. The time course of the regulatory effects differed among the individual growth factors and combinations. Growth factor-induced changes in growth factor protein production by articular chondrocytes generally corresponded to the changes in gene expression patterns. These studies suggest that interactions among IGF-I, FGF-2, and TGF-beta 1 substantially modulate their regulatory functions. The results may help guide the application of growth factors to articular cartilage repair.
引用
收藏
页码:6697 / 6704
页数:8
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