Regulation of skeletal development by the Runx family of transcription factors

被引:282
作者
Komori, T [1 ]
机构
[1] Nagasaki Univ, Div Oral Cytol & Cell Biol, Dept Dev & Reconstruct Med, Grad Sch Biomed Sci, Nagasaki 8528588, Japan
关键词
Runx2; Cbfa1; Runx3; Cbfb; osteoblast; chondrocyte; lhh;
D O I
10.1002/jcb.20420
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
The Runx (runt-related protein) family of transcription factors plays importantroles in different tissues and cell lineages. Runx] determines commitment to the hematopoietic cell lineage and Runx2 determines commitment to the osteoblastic lineage. Cbf beta is required for Runx1 - and Runx2-dependent transcriptional regulation. Runx2 interacts with many other transcription factors and co-regulators in the transcriptional regulation of its target genes. Runx2 is essential for the commitment of multipotent mesenchymal cells into the osteoblastic lineage and inhibits adipocyte differentiation. Runx2 induces the gene expression of hone matrix proteins, while keeping the osteoblastic cells in an immature stage. Runx2 and Runx3 have redundant functions in chondrocytes, and they are essential for chondrocyte maturation. Runx2 directly induces Indian hedgehog (Ihh) expression and co-ordinates the proliferation and differentiation of chondrocytes. Therefore, elucidation of the signaling pathways through Runx2 and Runx3 will unravel the complex mechanism of skeletal development. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:445 / 453
页数:9
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