Use of Bone Morphogenic Protein-7 as a Treatment for Osteoarthritis

被引:39
作者
Badlani, Neil [1 ]
Oshima, Yasushi [1 ]
Healey, Rob [1 ]
Coutts, Richard [1 ]
Amiel, David [1 ]
机构
[1] Univ Calif San Diego, Dept Orthopaed Surg, La Jolla, CA 92093 USA
关键词
HUMAN OSTEOGENIC PROTEIN-1; HUMAN ARTICULAR CHONDROCYTES; RABBIT KNEE; CARTILAGE; REPAIR; MODEL; EXPRESSION; DEFECTS; OP-1; PROTEOGLYCAN;
D O I
10.1007/s11999-008-0569-9
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
100224 [整形外科学];
摘要
Osteoarthritis is a degenerative disorder resulting from breakdown of articular cartilage. Previous work has shown bone morphogenic protein-7 has a potential protective effect on cartilage during the development of osteoarthritis. The purpose of this study was to determine whether bone morphogenic protein-7 could decrease the amount of cartilage degradation in preexisting osteoarthritis. The rabbit ACLT model was used as a model of osteoarthritis. Bone morphogenic protein-7 was delivered via Alzet osmotic pump to the joint 4 weeks after anterior cruciate ligament transection; thus cartilage injury was preexisting. The experimental group showed less cartilage degradation than the controls, with an average Outerbridge score of 1.9 versus 2.6 for the controls. Histomorphometry showed a trend toward less cartilage degradation in the bone morphogenic protein-7 group when compared with controls. Semiquantitative real-time polymerase chain reaction showed a considerably greater expression of aggrecan in the bone morphogenic protein-7-treated cartilage when compared with controls and less expression of matrix metalloproteinase-3 and matrix metalloproteinase-13, important catabolic mediators. The synovial tissue of the experimental group also showed considerably less expression of matrix metalloproteinase-3, matrix metalloproteinase-13, and aggrecanase. These results indicate bone morphogenic protein-7 may reduce degradation of articular cartilage in osteoarthritis.
引用
收藏
页码:3221 / 3229
页数:9
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