A role for the BMP antagonist chordin in endochondral ossification

被引:74
作者
Zhang, DH [1 ]
Ferguson, CM [1 ]
O'Keefe, RJ [1 ]
Puzas, JE [1 ]
Rosier, RN [1 ]
Reynolds, PR [1 ]
机构
[1] Univ Rochester, Sch Med & Dent, Dept Orthoped, Rochester, NY USA
关键词
bone morphogenetic proteins; chordin; chondrocyte differentiation; endochondral ossification; limb growth;
D O I
10.1359/jbmr.2002.17.2.293
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bone morphogenetic proteins (BMPs) are ubiquitous regulators of cellular growth and differentiation. A variety of processes modulate BMP activity, including negative regulation by several distinct binding proteins. One such BMP antagonist chordin has a role in axis determination and neural induction in the early embryo. In this study, a role for chordin during endochondral ossification has been investigated. During limb development, Chordin expression was detected only at the distal ends of the skeletal elements. In cultured embryonic sternal chondrocytes, Chordin expression was related inversely to the stages of maturation. Further, treating cultured chondrocytes with chordin interfered with maturation induced by treatment with BMP-2. These results suggest that chordin may negatively regulate chondrocyte maturation and limb growth in vivo. To address this hypothesis, chordin protein was expressed ectopically in Hamburger-Hamilton (HH) stage 25-27 embryonic chick limbs. The phenotypic changes and alteration of gene expression in treated limbs revealed that overexpression of chordin protein delayed chondrocyte maturation in developing skeletal elements. In summary, these findings strongly support a role for chordin as a negative regulator of endochondral ossification.
引用
收藏
页码:293 / 300
页数:8
相关论文
共 40 条
[31]   Cloning of the chick BMP1/Tolloid cDNA and expression in skeletal tissues [J].
Reynolds, SD ;
Zhang, DH ;
Puzas, JE ;
O'Keefe, RJ ;
Rosier, RN ;
Paul, R ;
Reynolds, PR .
GENE, 2000, 248 (1-2) :233-243
[32]  
Romano PR, 1998, J CELL SCI, V111, P803
[33]   Targeted expression of constitutively active receptors for parathyroid hormone and parathyroid hormone-related peptide delays endochondral bone formation and rescues mice that lack parathyroid hormone-related peptide [J].
Schipani, E ;
Lanske, B ;
Hunzelman, J ;
Luz, A ;
Kovacs, CS ;
Lee, K ;
Pirro, A ;
Kronenberg, HM ;
Juppner, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (25) :13689-13694
[34]  
Streit A, 1998, DEVELOPMENT, V125, P507
[35]   Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein [J].
Vortkamp, A ;
Lee, K ;
Lanske, B ;
Segre, GV ;
Kronenberg, HM ;
Tabin, CJ .
SCIENCE, 1996, 273 (5275) :613-622
[36]   Targeted overexpression of parathyroid hormone-related peptide in chondrocytes causes chondrodysplasia and delayed endochondral bone formation [J].
Weir, EC ;
Philbrick, WM ;
Amling, M ;
Neff, LA ;
Baron, R ;
Broadus, AE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (19) :10240-10245
[37]   BONE MORPHOGENETIC PROTEIN-4 IS REQUIRED FOR MESODERM FORMATION AND PATTERNING IN THE MOUSE [J].
WINNIER, G ;
BLESSING, M ;
LABOSKY, PA ;
HOGAN, BLM .
GENES & DEVELOPMENT, 1995, 9 (17) :2105-2116
[38]  
Zhang HB, 1996, DEVELOPMENT, V122, P2977
[39]   The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4 [J].
Zimmerman, LB ;
DeJesusEscobar, JM ;
Harland, RM .
CELL, 1996, 86 (04) :599-606
[40]   Distinct roles of type I bone morphogenetic protein receptors in the formation and differentiation of cartilage [J].
Zou, HY ;
Wieser, R ;
Massague, J ;
Niswander, L .
GENES & DEVELOPMENT, 1997, 11 (17) :2191-2203