Fra-2/AP-1 controls bone formation by regulating osteoblast differentiation and collagen production

被引:120
作者
Bozec, Aline [1 ]
Bakiri, Latifa [1 ]
Jimenez, Maria [1 ]
Schinke, Thorsten [2 ]
Amling, Michael [2 ]
Wagner, Erwin F. [1 ]
机构
[1] Spanish Natl Canc Ctr, Canc Cell Biol Program, BBVA Fdn, Genes Dev & Dis Grp, E-28029 Madrid, Spain
[2] Univ Med Ctr Hamburg Eppendorf, Dept Osteol & Biomech, D-20246 Hamburg, Germany
基金
欧洲研究理事会;
关键词
MOUSE OSTEOCALCIN GENE; OSTEOSARCOMA CELL-LINE; GROWTH-FACTOR-BETA; TRANSGENIC MICE; IN-VITRO; EXPRESSION; PROMOTER; MASS; ADIPOGENESIS; ACTIVATOR;
D O I
10.1083/jcb.201002111
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
T he activator protein-1 (AP-1) transcription factor complex, in particular the Fos proteins, is an important regulator of bone homeostasis. Fra-2 (Fosl2), a Fos-related protein of the AP-1 family, is expressed in bone cells, and newborn mice lacking Fra-2 exhibit defects in chondrocytes and osteoclasts. Here we show that Fra-2-deficient osteoblasts display a differentiation defect both in vivo and in vitro. Moreover, Fra-2-overexpressing mice are osteosclerotic because of increased differentiation of osteoblasts, which appears to be cell autonomous. Importantly, the osteoblast-specific osteocalcin (Oc) gene and collagen1 alpha 2 (col1 alpha 2) are transcriptional targets of Fra-2 in both murine and human bone cells. In addition, Fra-2, Oc, and col1 are expressed in stromal cells of human chondroblastic and osteoblastic osteosarcomas (Os's) as well as during osteoblast differentiation of human Os cell lines. These findings reveal a novel function of Fra-2/AP-1 as a positive regulator of bone and matrix formation in mice and humans.
引用
收藏
页码:1093 / 1106
页数:14
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