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Regulation of osteoblast differentiation by transcription factors

Journal of Cellular Biochemistry · 2006 · Vol. 99(5) · pp. 1233–1239
Toshihisa Komori

Abstract

Runx2, osterix, and beta-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, beta-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.

Bone Metabolism and DiseasesNF-κB Signaling PathwaysTGF-β signaling in diseasesRUNX2OsteoblastCell biologyTranscription factorMesenchymal stem cellDLX5AP-1 transcription factorATF4ChemistryCellular differentiation

MeSH terms

Sp7 Transcription FactorAnimalsCell DifferentiationHumansOsteoblastsTranscription FactorsCell LineageCore Binding Factor Alpha 1 Subunitbeta CateninMice
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Regulation of osteoblast differentiation by transcription factors
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