Critical roles for collagenase-3 (Mmp13) in development of growth and in endochondral plate cartilage ossification

被引:453
作者
Inada, M
Wang, YM
Byrne, MH
Rahman, MU
Miyaura, C
López-Otín, C
Krane, SM
机构
[1] Harvard Univ, Sch Med, Ctr Immunol & Inflammatory Dis, Dept Med, Boston, MA 02129 USA
[2] Massachusetts Gen Hosp, Boston, MA 02129 USA
[3] Tokyo Univ Agr & Technol, Dept Biotechnol & Life Sci, Koganei, Tokyo 1848588, Japan
[4] Univ Oviedo, Inst Univ Oncol, Dept Bioquim & Biol Mol, E-33006 Oviedo, Spain
关键词
collagen; extracellular matrix; vascularization;
D O I
10.1073/pnas.0407788101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Collagenase-3 (MMP13), a member of the matrix metalloproteinase (MMP) family of neutral endopeptidases, is expressed in the skeleton during embryonic development and is highly overexpressed in human carcinomas and in chondrocytes and synovial cells in rheumatoid arthritis and osteoarthritis. To determine the functional roles of Mmp13, we generated Mmp13-null mice that showed profound defects in growth plate cartilage with markedly increased hypertrophic domains as well as delay in endochondral ossification and formation and vascularization of primary ossification centers. Absence of Mmp13 resulted in significant interstitial collagen accumulation due, in part, to the lack of appropriate collagenase-mediated cleavage that normally occurs in growth plates and primary ossification centers. Cartilaginous growth plate abnormalities persisted in adult mice and phenocopied defects observed in human hereditary chondrodysplasias. Our findings demonstrate a unique role of Mmp13 in skeletal development.
引用
收藏
页码:17192 / 17197
页数:6
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