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
[11]   IMMUNOLOCALIZATION OF METALLOPROTEINASES AND THEIR INHIBITOR IN THE RABBIT GROWTH PLATE [J].
BROWN, CC ;
HEMBRY, RM ;
REYNOLDS, JJ .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1989, 71A (04) :580-593
[12]   Altered fracture repair in the absence of MMP9 [J].
Colnot, C ;
Thompson, Z ;
Miclau, T ;
Werb, Z ;
Helms, JA .
DEVELOPMENT, 2003, 130 (17) :4123-4133
[13]   Perlecan maintains the integrity of cartilage and some basement membranes [J].
Costell, M ;
Gustafsson, E ;
Aszódi, A ;
Mörgelin, M ;
Bloch, W ;
Hunziker, E ;
Addicks, K ;
Timpl, R ;
Fässler, R .
JOURNAL OF CELL BIOLOGY, 1999, 147 (05) :1109-1122
[14]   Enzymes active in the areas undergoing cartilage resorption during the development of the secondary ossification center in the tibiae of rats aged 0-21 days: II. Two proteinases, gelatinase B and collagenase-3, are implicated in the lysis of collagen fibrils [J].
Davoli, MA ;
Lamplugh, L ;
Beauchemin, A ;
Chan, K ;
Mordier, S ;
Mort, JS ;
Murphy, G ;
Docherty, AJP ;
Leblond, CP ;
Lee, ER .
DEVELOPMENTAL DYNAMICS, 2001, 222 (01) :71-88
[15]   LOCALIZATION OF COLLAGENASE IN THE GROWTH PLATE OF RACHITIC RATS [J].
DEAN, DD ;
MUNIZ, OE ;
BERMAN, I ;
PITA, JC ;
CARRENO, MR ;
WOESSNER, JF ;
HOWELL, DS .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (02) :716-722
[16]   Localisation of matrix metalloproteinases and TIMP-2 in resorbing mouse bone [J].
Dew, G ;
Murphy, G ;
Stanton, H ;
Vallon, R ;
Angel, P ;
Reynolds, JJ ;
Hembry, RM .
CELL AND TISSUE RESEARCH, 2000, 299 (03) :385-394
[17]   New functions for the matrix metalloproteinases in cancer progression [J].
Egeblad, M ;
Werb, Z .
NATURE REVIEWS CANCER, 2002, 2 (03) :161-174
[18]   Matrix metalloproteinase 9 and vascular endothelial growth factor are essential for osteoclast recruitment into developing long bones [J].
Engsig, MT ;
Chen, QJ ;
Vu, TH ;
Pedersen, AC ;
Therkidsen, B ;
Lund, LR ;
Henriksen, K ;
Lenhard, T ;
Foged, NT ;
Werb, Z ;
Delaisse, JM .
JOURNAL OF CELL BIOLOGY, 2000, 151 (04) :879-889
[19]   DEVELOPMENTAL EXPRESSION OF THE ENDOGENOUS TIMP GENE AND A TIMP-1ACZ FUSION GENE IN TRANSGENIC MICE [J].
FLENNIKEN, AM ;
WILLIAMS, BRG .
GENES & DEVELOPMENT, 1990, 4 (07) :1094-1106
[20]  
GACK S, 1995, CELL GROWTH DIFFER, V6, P759