Regulation of osteoblast differentiation by transcription factors

被引:878
作者
Komori, Toshihisa [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Dept Dev & Reconstruct Med, Div Cell Biol, Nagasaki 8528588, Japan
关键词
Runx2; osterix; beta-catenin; osteoblast; transcription factor;
D O I
10.1002/jcb.20958
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Runx2, osterix, and beta-catenin are essential for osteoblast differentiation. Runx2 directs multipotent mesenchymal cellstoan osteoblastic lineage, and inhibitsthem from differentiating into the adipocytic and chondrocytic lineages. After differentiating to preosteoblasts, beta-catenin, osterix, and Runx2 directthem to immature osteoblasts, which produce bone matrix proteins, blocking their potential to differentiate into the chondrocytic lineage. Runx2 inhibits osteoblast maturation and the transition into osteocytes, keeping osteoblasts in an immature stage. Other transcription factors including Msxl, Msx2, Dlx5, Dlx6, Twist, AP1 (Fos/Jun), Knox-20, Sp3, and ATF4 are also involved in osteoblast differentiation. To gain an understanding of bone development, it is importantto position these transcription factors to the right places in the processes of osteoblast differentiation.
引用
收藏
页码:1233 / 1239
页数:7
相关论文
共 33 条
[11]   Sequential roles of Hedgehog and Wnt signaling in osteoblast development [J].
Hu, HL ;
Hilton, MJ ;
Tu, XL ;
Yu, K ;
Ornitz, DM ;
Long, F .
DEVELOPMENT, 2005, 132 (01) :49-60
[12]   Reciprocal roles of Msx2 in regulation of osteoblast and adipocyte differentiation [J].
Ichida, F ;
Nishimura, R ;
Hata, K ;
Matsubara, T ;
Ikeda, F ;
Hisada, K ;
Yatani, H ;
Cao, X ;
Komori, T ;
Yamaguchi, A ;
Yoneda, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (32) :34015-34022
[13]   Msx2 and Twist cooperatively control the development of the neural crest-derived skeletogenic mesenchyme of the murine skull vault [J].
Ishii, M ;
Merrill, AE ;
Chan, YS ;
Gitelman, I ;
Rice, DPC ;
Sucov, HM ;
Maxson, RE .
DEVELOPMENT, 2003, 130 (24) :6131-6142
[14]  
KANATANI N, 2006, IN PRESS DEV BIOL
[15]   Repression of Runx2 function by TGF-β through recruitment of class II histone deacetylases by Smad3 [J].
Kang, JS ;
Alliston, T ;
Delston, R ;
Derynck, R .
EMBO JOURNAL, 2005, 24 (14) :2543-2555
[16]   Multilineage differentiation of Cbfa1-deficient calvarial cells in vitro [J].
Kobayashi, H ;
Gao, YH ;
Ueta, C ;
Yamaguchi, A ;
Komori, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (02) :630-636
[17]   NFAT and Osterix cooperatively regulate bone formation [J].
Koga, T ;
Matsui, Y ;
Asagiri, M ;
Kodama, T ;
de Crombrugghe, B ;
Nakashima, K ;
Takayanagi, H .
NATURE MEDICINE, 2005, 11 (08) :880-885
[18]   Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts [J].
Komori, T ;
Yagi, H ;
Nomura, S ;
Yamaguchi, A ;
Sasaki, K ;
Deguchi, K ;
Shimizu, Y ;
Bronson, RT ;
Gao, YH ;
Inada, M ;
Sato, M ;
Okamoto, R ;
Kitamura, Y ;
Yoshiki, S ;
Kishimoto, T .
CELL, 1997, 89 (05) :755-764
[19]   Regulation of skeletal development by the Runx family of transcription factors [J].
Komori, T .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2005, 95 (03) :445-453
[20]   ΔFosB induces osteosclerosis and decreases adipogenesis by two independent cell-autonomous mechanisms [J].
Kveiborg, M ;
Sabatakos, G ;
Chiusaroli, R ;
Wu, ML ;
Philbrick, WM ;
Horne, WC ;
Baron, R .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (07) :2820-2830