β-Catenin in the race to fracture repair:: in it to Wnt

被引:51
作者
Silkstone, David
Hong, Helen
Alman, Benjamin A. [1 ,2 ]
机构
[1] Hosp Sick Children, Program Dev & Stem Cell Biol, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, AJ Latner Chair Orthopaed Surg, Toronto, ON M5G 1X8, Canada
来源
NATURE CLINICAL PRACTICE RHEUMATOLOGY | 2008年 / 4卷 / 08期
关键词
chondrocytes; embryonic bone development; fracture repair; osteoblasts; Wnt/beta-catenin;
D O I
10.1038/ncprheum0838
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Wnt/beta-catenin pathway regulates multiple biological events during embryonic development, including bone formation. Fracture repair recapitulates some of the processes of normal bone development, such as the formation of bone from a cartilaginous template, and many cell-signaling pathways that underlie bone development are activated during the repair process. The Wnt/beta-catenin signaling pathway is activated during fracture repair, and dysregulation of this pathway alters the normal bone-healing response. In early pluripotent mesenchymal stem cells, Wnt/beta-catenin signaling needs to be precisely regulated to facilitate the differentiation of osteoblasts; by contrast, beta-catenin is not needed for chondrocyte differentiation. Once mesenchymal stem cells are committed to the osteoblast lineage, activation of Wnt/beta-catenin signaling enhances bone formation. This activity suggests that the Wnt/beta-catenin pathway is a therapeutic target during bone repair. Indeed, treatments that activate Wnt/beta-catenin signaling, such as lithium, increase bone density and also enhance healing.
引用
收藏
页码:413 / 419
页数:7
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