Regulation of Osteoblast Differentiation by Runx2

被引:435
作者
Komori, Toshihisa [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Unit Basic Med Sci, Dept Cell Biol, Nagasaki 8528588, Japan
来源
OSTEOIMMUNOLOGY: INTERACTIONS OF THE IMMUNE AND SKELETAL SYSTEMS II | 2010年 / 658卷
关键词
Runx2; Sp7; Canonical Wnt Signaling; Osteoblast; Osteopontin; Osteocalcin; BONE-FORMATION; TRANSCRIPTION FACTOR; SKELETAL DEVELOPMENT; CBFA1; CONTRIBUTES; EXPRESSION; GENE; MAINTENANCE; PROGENITORS; HEDGEHOG; FAMILY;
D O I
10.1007/978-1-4419-1050-9_5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Runx2 protein is first detected in preosteoblasts, and the expression is upregulated in immature osteoblasts, but downregulated in mature osteoblasts. Runx2 is the first transcription factor required for determination of the osteoblast lineage, while Sp7 and canonical Wnt-signaling further direct the fate of mesenchymal cells to osteoblasts, blocking their differentiation into chondrocytes. Runx2 induces the differentiation of multipotent mesenchymal cells into immature osteoblasts, directing the formation of immature bone, but Runx2 inhibits osteoblast maturation and mature bone formation. Normally, the protein level of Runx2 in osteoblasts reduces during bone development, and osteoblasts acquire mature phenotypes, which are required for mature bone formation. Furthermore, Runx2 triggers the expression of major bone matrix genes during the early stages of osteoblast differentiation, but Runx2 is not essential for the maintenance of these gene expressions in mature osteoblasts.
引用
收藏
页码:43 / 49
页数:7
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