Dissociation between bone resorption and bone formation in osteopenic transgenic mice

被引:163
作者
Corral, DA
Amling, M
Priemel, M
Loyer, E
Fuchs, S
Ducy, P
Baron, R
Karsenty, G
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Urol, Houston, TX 77030 USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Radiol, Houston, TX 77030 USA
[5] Univ Hamburg, Dept Trauma Surg, D-20246 Hamburg, Germany
[6] Univ Hamburg, Dept Bone Pathol, D-20246 Hamburg, Germany
[7] Yale Univ, Sch Med, Dept Cell Biol & Orthoped, New Haven, CT 06510 USA
关键词
D O I
10.1073/pnas.95.23.13835
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bone mass is maintained constant in vertebrates through bone remodeling (BR), BR is characterized by osteoclastic resorption of preexisting bone followed by ne novo bone formation by osteoblasts. This sequence of events and the fact that bone mass remains constant in physiological situation lead to the assumption that resorption and formation are regulated by each other during BR, Recent evidence shows that cells of the osteoblastic lineage are involved in osteoclast differentiation. However, the existence of a functional link between the two activities, formation and resorption, has never been shown in vivo. To define the role of bone formation in the control of bone resorption, we generated an inducible osteoblast ablation mouse model. These mice developed a reversible osteopenia, Functional analyses showed that in the absence of bone formation, bone resorption continued to occur normally, leading to an osteoporosis of controllable severity, whose appearance could be prevented by an antiresorptive agent. This study establishes that bone formation and/or bone mass do not control the extent of bone resorption in vivo.
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页码:13835 / 13840
页数:6
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