Inada Masaki, Wang Yingmin, Byrne Michael H, Rahman Mahboob U, Miyaura Chisato, López-Otín Carlos, Krane Stephen M
Center for Immunology and Inflammatory Diseases, Department of Medicine, Harvard Medical School and Massachusetts General Hospital, Building 149, 13th Street, Room 8301, Boston, MA 02129, USA.
Proc Natl Acad Sci U S A. 2004 Dec 7;101(49):17192-7. doi: 10.1073/pnas.0407788101. Epub 2004 Nov 24.
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.
胶原酶-3(MMP13)是中性内肽酶基质金属蛋白酶(MMP)家族的成员之一,在胚胎发育期间于骨骼中表达,并且在人类癌症以及类风湿性关节炎和骨关节炎的软骨细胞与滑膜细胞中高度过表达。为了确定Mmp13的功能作用,我们培育出了Mmp13基因敲除小鼠,这些小鼠在生长板软骨中表现出严重缺陷,肥大区域明显增加,同时软骨内骨化以及初级骨化中心的形成和血管化出现延迟。Mmp13的缺失导致了显著的间质胶原积累,部分原因是生长板和初级骨化中心中正常发生的胶原酶介导的切割缺乏。软骨生长板异常在成年小鼠中持续存在,并且复制了在人类遗传性软骨发育不良中观察到的缺陷。我们的研究结果证明了Mmp13在骨骼发育中的独特作用。