Critical molecular switches involved in BMP-2-induced osteogenic differentiation of mesenchymal cells

被引:326
作者
Ryoo, HM
Lee, MH
Kim, YJ
机构
[1] Seoul Natl Univ, Sch Dent, Dept Cell & Dev Biol, Seoul 110749, South Korea
[2] Seoul Natl Univ, Dent Res Inst, Seoul 110749, South Korea
[3] Kyungpook Natl Univ, Sch Dent, Dept Biochem, Taegu 700422, South Korea
[4] Kyungpook Natl Univ, Skeletal Dis Genome Res Ctr, Taegu 700422, South Korea
关键词
BMP-2; TGF-beta; Smad; Runx2; Osx; Dlx5; Msx2; osteoblast; differentiation; bone;
D O I
10.1016/j.gene.2005.10.011
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Bone morphogenetic protein (BMP)-2 strongly induces bone formation. Introduction of the protein in muscle tissue results in ectopic bone formation. Similarly, BMP-2 treatment also stimulates the in vitro transdifferentiation of myogenic cells to osteogenic cells. The establishment of an in vitro model system has enabled the investigation of intracellular events including BMP receptor activation, BMP-2-induced R-Smad activation, and kinase activation, and the role of osteogenic transcription factors, such as Runx2, Osx, Dlx5, and Msx2. Many reviews have addressed events downstream of BMP-receptor binding but few deal with molecular cascades involved in BMP-2-induced osteogenesis. We focus on critical molecular switches, especially transcription factors, and several kinase pathways involved in osteogenic differentiation. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:51 / 57
页数:7
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