Update on Wnt signaling in bone cell biology and bone disease

被引:303
|
作者
Monroe, David G. [2 ]
McGee-Lawrence, Meghan E. [1 ]
Oursler, Merry Jo [2 ,3 ]
Westendorf, Jennifer J. [1 ,3 ]
机构
[1] Mayo Clin, Dept Orthoped Surg, Div Orthoped Surg, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Med, Endocrine Res Unit, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
关键词
Lrp5; Lrp6; Sclerostin; beta-catenin; R-spondin; Bone mineral density; Polymorphisms; FRIZZLED-RELATED PROTEIN-1; RECEPTOR-RELATED PROTEIN-5; GENOME-WIDE ASSOCIATION; THYMIC EPITHELIAL-CELLS; MESENCHYMAL STEM-CELLS; VAN-BUCHEM-DISEASE; ENHANCER FACTOR-I; BETA-CATENIN; PARATHYROID-HORMONE; NEGATIVE REGULATOR;
D O I
10.1016/j.gene.2011.10.044
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
For more than a decade, Wnt signaling pathways have been the focus of intense research activity in bone biology laboratories because of their importance in skeletal development, bone mass maintenance, and therapeutic potential for regenerative medicine. It is evident that even subtle alterations in the intensity, amplitude, location, and duration of Wnt signaling pathways affects skeletal development, as well as bone remodeling, regeneration, and repair during a lifespan. Here we review recent advances and discrepancies in how Wnt/Lrp5 signaling regulates osteoblasts and osteocytes, introduce new players in Wnt signaling pathways that have important roles in bone development, discuss emerging areas such as the role of Wnt signaling in osteoclastogenesis, and summarize progress made in translating basic studies to clinical therapeutics and diagnostics centered around inhibiting Wnt pathway antagonists, such as sclerostin, Dkk1 and Sfrp1. Emphasis is placed on the plethora of genetic studies in mouse models and genome wide association studies that reveal the requirement for and crucial roles of Wnt pathway components during skeletal development and disease. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 18
页数:18
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