1. TGF-[beta]1--induced migration of bone mesenchymal stem cells couples bone resorption with formation
- Author
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Tang, Yi, Wu, Xiangwei, Lei, Weiqi, Pang, Lijuan, Wan, Chao, Shi, Zhenqi, Zhao, Ling, Nagy, Timothy R., Peng, Xinyu, Hu, Junbo, Feng, Xu, Van Hul, Wim, Wan, Mei, and Cao, Xu
- Subjects
Bone resorption -- Care and treatment ,Bone resorption -- Research ,Transforming growth factors -- Physiological aspects ,Transforming growth factors -- Research ,Bone regeneration -- Health aspects ,Bone regeneration -- Research ,Cellular signal transduction -- Physiological aspects ,Cellular signal transduction -- Research ,Stem cells -- Physiological aspects ,Stem cells -- Research - Abstract
Bone remodeling depends on the precise coordination of bone resorption and subsequent bone formation. Disturbances of this process are associated with skeletal diseases, such as Camurati-Engelmann disease (CED). We show using in vitro and in vivo models that active TGF-[beta]1 released during bone resorption coordinates bone formation by inducing migration of bone marrow stromal cells, also known as bone mesenchymal stem cells, to the bone resorptive sites and that this process is mediated through a SMAD signaling pathway. Analyzing mice carrying a CED-derived mutant TGFB1 (encoding TGF-[beta]1), which show the typical progressive diaphyseal dysplasia seen in the human disease, we found high levels of active TGF-[beta]1 in the bone marrow. Treatment with a TGF-[beta] type I receptor inhibitor partially rescued the uncoupled bone remodeling and prevented the fractures. Thus, as TGF-[beta]1 functions to couple bone resorption and formation, modulation of TGF-[beta]1 activity could be an effective treatment for bone remodeling diseases., In the adult skeleton, bone is continuously being formed and resorbed, not only to maintain mineral homeostasis but also to cope with the microfractures that occur as a consequence of [...]
- Published
- 2009