Regulation of osteoblast differentiation by transcription factors

T Komori - Journal of cellular biochemistry, 2006 - Wiley Online Library
Journal of cellular biochemistry, 2006Wiley Online Library
Abstract Runx2, osterix, and β‐catenin are essential for osteoblast differentiation. Runx2
directs multipotent mesenchymal cells to an osteoblastic lineage, and inhibits them from
differentiating into the adipocytic and chondrocytic lineages. After differentiating to
preosteoblasts, β‐catenin, osterix, and Runx2 direct them 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 …
Abstract
Runx2, osterix, and β‐catenin are essential for osteoblast differentiation. Runx2 directs multipotent mesenchymal cells to an osteoblastic lineage, and inhibits them from differentiating into the adipocytic and chondrocytic lineages. After differentiating to preosteoblasts, β‐catenin, osterix, and Runx2 direct them 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 Msx1, 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 important to position these transcription factors to the right places in the processes of osteoblast differentiation. J. Cell. Biochem. 99: 1233–1239, 2006. © 2006 Wiley‐Liss, Inc.
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