Bone morphogenetic protein 2-induced osteoblast differentiation requires smad-mediated down-regulation of Cdk6

被引:119
作者
Ogasawara, T
Kawaguchi, H
Jinno, S
Hoshi, K
Itaka, K
Takato, T
Nakamura, K
Okayama, H
机构
[1] Univ Tokyo, Grad Sch Med, Dept Biochem & Mol Biol, Tokyo 1130033, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Sensory & Motor Syst Med, Tokyo 1130033, Japan
关键词
D O I
10.1128/mcb.24.15.6560-6568.2004
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
Because a temporal arrest in the G, phase of the cell cycle is thought to be a prerequisite for cell differentiation, we investigated cell cycle factors that critically influence the differentiation of mouse osteoblastic MC3T3-E1 cells induced by bone morphogenetic protein 2 (BMP-2), a potent inducer of osteoblast differentiation. Of the G, cell cycle factors examined, the expression of cyclin-dependent kinase 6 (Cdk6) was found to be strongly down-regulated by BMP-2/Smads signaling, mainly via transcriptional repression. The enforced expression of Cdk6 blocked BMP-2-induced osteoblast differentiation to various degrees, depending on the level of its overexpression. However, neither BMP-2 treatment nor Cdk6 overexpression significantly affected cell proliferation, suggesting that the inhibitory effect of Cdk6 on cell differentiation was exerted by a mechanism that is largely independent of its cell cycle regulation. These results indicate that Cdk6 is a critical regulator of BMP-2-induced osteoblast differentiation and that its Smads-mediated down-regulation is essential for efficient osteoblast differentiation.
引用
收藏
页码:6560 / 6568
页数:9
相关论文
共 33 条
[1]   Smad6 as a transcriptional corepressor [J].
Bai, ST ;
Shi, XM ;
Yang, XL ;
Cao, X .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) :8267-8270
[2]   Overexpression of Cdk6-cyclin D3 highly sensitizes cells to physical and chemical transformation [J].
Chen, QH ;
Lin, J ;
Jinno, S ;
Okayama, H .
ONCOGENE, 2003, 22 (07) :992-1001
[3]   MICE LACKING P21(C/P1/WAF1) UNDERGO NORMAL DEVELOPMENT, BUT ARE DEFECTIVE IN G1 CHECKPOINT CONTROL [J].
DENG, CX ;
ZHANG, PM ;
HARPER, JW ;
ELLEDGE, SJ ;
LEDER, P .
CELL, 1995, 82 (04) :675-684
[4]   Inhibition of E-selectin gene expression by transforming growth factor β in endothelial cells involves coactivator integration of Smad and nuclear factor κB-mediated signals [J].
DiChiara, MR ;
Kiely, JM ;
Gimbrone, MA ;
Lee, ME ;
Perrella, MA ;
Topper, JN .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (05) :695-704
[5]   TUMOR-SUPPRESSOR GENES [J].
HINDS, PW ;
WEINBERG, RA .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (01) :135-141
[6]   SMADs:: mediators and regulators of TGF-β signaling [J].
Kretzschmar, M ;
Massague, J .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1998, 8 (01) :103-111
[7]   Runx2 is a common target of transforming growth factor β1 and bone morphogenetic protein 2, and cooperation between Runx2 and Smad5 induces osteoblast-specific gene expression in the pluripotent mesenchymal precursor cell line C2C12 [J].
Lee, KS ;
Kim, HJ ;
Li, QL ;
Chi, XZ ;
Ueta, C ;
Komori, T ;
Wozney, JM ;
Kim, EG ;
Choi, JY ;
Ryoo, HM ;
Bae, SC .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (23) :8783-8792
[8]   Cdk6-cyclin D3 complex evades inhibition by inhibitor proteins and uniquely controls cell's proliferation competence [J].
Lin, J ;
Jinno, S ;
Okayama, H .
ONCOGENE, 2001, 20 (16) :2000-2009
[9]   Interaction and functional cooperation of NF-κB with Smads -: Transcriptional regulation of the junB promoter [J].
López-Rovira, T ;
Chalaux, E ;
Rosa, JL ;
Bartrons, R ;
Ventura, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (37) :28937-28946
[10]   CDK6 blocks differentiation: coupling cell proliferation to the block to differentiation in leukemic cells [J].
Matushansky, I ;
Radparvar, F ;
Skoultchi, AI .
ONCOGENE, 2003, 22 (27) :4143-4149