Matrix remodeling during endochondral ossification

被引:342
作者
Ortega, N [1 ]
Behonick, DJ [1 ]
Werb, Z [1 ]
机构
[1] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.tcb.2003.12.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Endochondral ossification, the process by which most of the skeleton is formed, is a powerful system for studying various aspects of the biological response to degraded extracellular matrix (ECM). In addition, the dependence of endochondral ossification upon neovascularization and continuous ECM remodeling provides a good model for studying the role of the matrix metalloproteases (MMPs) not only as simple effectors of ECM degradation but also as regulators of active signal-inducers for the initiation of endochondral ossification. The daunting task of elucidating their specific role during endochondral ossification has been facilitated by the development of mice deficient for various members of this family. Here, we discuss the ECM and its remodeling as one level of molecular regulation for the process of endochondral ossification, with special attention to the MMPs.
引用
收藏
页码:86 / 93
页数:8
相关论文
共 59 条
[41]   Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome [J].
Martignetti, JA ;
Al Aqeel, A ;
Al Sewairi, W ;
Boumah, CE ;
Kambouris, M ;
Al Mayouf, S ;
Sheth, KV ;
Al Eid, W ;
Dowling, O ;
Harris, J ;
Glucksman, MJ ;
Bahabri, S ;
Meyer, BF ;
Desnick, RJ .
NATURE GENETICS, 2001, 28 (03) :261-265
[42]  
MATTOT V, 1995, J CELL SCI, V108, P529
[43]   EXPRESSION OF 92-KD TYPE-IV COLLAGENASE (GELATINASE-B) IN THE OSTEOCLAST LINEAGE DURING MOUSE DEVELOPMENT [J].
REPONEN, P ;
SAHLBERG, C ;
MUNAUT, C ;
THESLEFF, I ;
TRYGGVASON, K .
JOURNAL OF CELL BIOLOGY, 1994, 124 (06) :1091-1102
[44]   Activation of a recombinant membrane type 1-matrix metalloproteinase (MT1-MMP) by furin and its interaction with tissue inhibitor of metalloproteinases (TIMP)-2 [J].
Sato, H ;
Kinoshita, T ;
Takino, T ;
Nakayama, K ;
Seiki, M .
FEBS LETTERS, 1996, 393 (01) :101-104
[45]  
Sato T, 1997, J CELL SCI, V110, P589
[46]   Parathyroid hormone-related peptide (PTHrP)-dependent and -independent effects of transforming growth factor β (TGF-β) on endochondral bone formation [J].
Serra, R ;
Karaplis, A ;
Sohn, P .
JOURNAL OF CELL BIOLOGY, 1999, 145 (04) :783-794
[47]  
StahleBackdahl M, 1997, LAB INVEST, V76, P717
[48]   Collagenase-3 (MMP-13) and integral membrane protein 2a (Itm2a) are marker genes of chondrogenic/osteoblastic cells in bone formation:: Sequential temporal, and spatial expression of Itm2a, alkaline phosphatase, MMP-13, and osteocalcin in the mouse [J].
Tuckermann, JP ;
Pittois, K ;
Partridge, NC ;
Merregaert, J ;
Angel, P .
JOURNAL OF BONE AND MINERAL RESEARCH, 2000, 15 (07) :1257-1265
[49]   Expression of cathepsins B, H, K, L, and S and matrix metalloproteinases 9 and 13 during chondrocyte hypertrophy and endochondral ossification in mouse fracture callus [J].
Uusitalo, H ;
Hiltunen, A ;
Söderström, M ;
Aro, HT ;
Vuorio, E .
CALCIFIED TISSUE INTERNATIONAL, 2000, 67 (05) :382-390
[50]   THE CYSTEINE SWITCH - A PRINCIPLE OF REGULATION OF METALLOPROTEINASE ACTIVITY WITH POTENTIAL APPLICABILITY TO THE ENTIRE MATRIX METALLOPROTEINASE GENE FAMILY [J].
VANWART, HE ;
BIRKEDALHANSEN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (14) :5578-5582