Role of N-cadherin in bone formation

被引:106
作者
Marie, PJ
机构
[1] Hop Lariboisiere, INSERM, U 349, F-75475 Paris 10, France
[2] Hop Lariboisiere, CNRS, F-75475 Paris 10, France
关键词
D O I
10.1002/jcp.10073
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell-cell adhesion mediated by cadherins is essential for the function of bone forming cells during osteogenesis. Here, the evidence that N-cadherin is an important regulator of osteoblast differentiation and osteogenesis is reviewed. Osteoblasts express a limited number of cadherins, including the classic N-cadherin. The expression profile of N-cadherin in osteoblasts during bone formation in vivo and in vitro suggests a role of this molecule in osteogenesis. Functional studies using neutralizing antibodies or antisense oligonucleotides indicate that N-cadherin is involved in the control the expression of osteoblast marker gene expression and differentiation. Cleavage of N-cadherin during osteoblast apoptosis also suggests a role of N-cadherin-mediated-cell-cell adhesion in osteoblast survival. Hormonal and local factors that regulate osteoblast function also regulate N-cadherin expression and subsequent cell-cell adhesion associated with osteoblast differentiation or survival. Signaling mechanisms involved in N-cadherin-mediated cell-cell adhesion and osteoblast gene expression have also been identified. Alterations of N-cadherin expression are associated with abnormal osteoblast differentiation and osteogenesis in pathological conditions. These findings indicate that N-cadherin plays a role in normal and pathological bone formation and provide some insight into the process involved in N-cadherin-mediated cell-cell adhesion and differentiation in osteoblasts. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:297 / 305
页数:9
相关论文
共 91 条
[61]  
NEWTON AC, 1995, J BIOL CHEM, V270, P28495, DOI 10.1074/jbc.270.48.28495
[62]   Is there a therapeutic opportunity to either prevent or treat osteopenic disorders by inhibiting marrow adipogenesis? [J].
Nuttall, ME ;
Gimble, JM .
BONE, 2000, 27 (02) :177-184
[63]   SPATIOTEMPORAL PROFILE OF N-CADHERIN EXPRESSION IN THE DEVELOPING LIMB MESENCHYME [J].
OBERLENDER, SA ;
TUAN, RS .
CELL ADHESION AND COMMUNICATION, 1994, 2 (06) :521-537
[64]  
OBERLENDER SA, 1994, DEVELOPMENT, V120, P177
[65]  
OKAZAKI M, 1994, J BIOL CHEM, V269, P12092
[66]   The transcription factor SOX9 regulates cell cycle and differentiation genes in chondrocytic CFK2 cells. [J].
Panda, DK ;
Miao, DS ;
Lefebvre, V ;
Hendy, GN ;
Goltzman, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (44) :41229-41236
[67]   INDUCTION OF THE NEURAL CELL-ADHESION MOLECULE AND NEURONAL AGGREGATION BY OSTEOGENIC PROTEIN-1 [J].
PERIDES, G ;
SAFRAN, RM ;
RUEGER, DC ;
CHARNESS, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (21) :10326-10330
[68]   The cadherin-catenin system: Implications for growth and differentiation of endocrine tissues [J].
Pötter, E ;
Bergwitz, C ;
Brabant, G .
ENDOCRINE REVIEWS, 1999, 20 (02) :207-239
[69]  
Quarles LD, 1996, J BONE MINER RES, V11, P1375
[70]   Developmental defects in mouse embryos lacking N-cadherin [J].
Radice, GL ;
Rayburn, H ;
Matsunami, H ;
Knudsen, KA ;
Takeichi, M ;
Hynes, RO .
DEVELOPMENTAL BIOLOGY, 1997, 181 (01) :64-78