Transcriptional Regulatory Cascades in Runx2-Dependent Bone Development

被引:2
|
作者
Liu, Tong Ming [1 ,2 ,3 ]
Lee, Eng Hin [2 ,3 ]
机构
[1] Genome Inst Singapore, Stem Cell & Dev Biol, Singapore 138672, Singapore
[2] Natl Univ Singapore, Dept Orthopaed Surg, Singapore 119260, Singapore
[3] Natl Univ Singapore, NUS Tissue Engn Program NUSTEP, Singapore 119260, Singapore
关键词
MESENCHYMAL STEM-CELLS; GROWTH-PLATE CHONDROCYTES; SAETHRE-CHOTZEN SYNDROME; OSTEOBLAST DIFFERENTIATION; IN-VITRO; CLEIDOCRANIAL DYSPLASIA; OSTEOGENIC DIFFERENTIATION; MORPHOGENETIC PROTEIN; CBFA1-DEFICIENT MICE; RUNX2; OVEREXPRESSION;
D O I
10.1089/ten.teb.2012.0527
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The development of the musculoskeletal system is a complex process that involves very precise control of bone formation and growth as well as remodeling during postnatal life. Although the understanding of the transcriptional mechanisms of osteogenesis has increased considerably, the molecular regulatory basis, especially the gene regulatory network of osteogenic differentiation, is still poorly understood. This review provides the reader with an overview of the key transcription factors that govern bone formation, highlighting their function and regulation linked to Runt-related transcription factor 2 (Runx2). Runx2 as the master transcription factor of osteoblast differentiation, Twist, Msh homeobox 2 (Msx2), and promyelocytic leukemia zinc-finger protein (PLZF) acting upstream of Runx2, Osterix (Osx) acting downstream of Runx2, and activating transcription factor 4 (ATF4) and zinc-finger protein 521 (ZFP521) acting as cofactors of Runx2 are discussed, and their relevance for tissue engineering is presented. References are provided for more in-depth personal study.
引用
收藏
页码:254 / 263
页数:10
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