Interleukin-11 as a stimulatory factor for bone formation prevents bone loss with advancing age in mice

被引:109
作者
Takeuchi, Y
Watanabe, S
Ishii, G
Takeda, S
Nakayama, K
Fukumoto, S
Kaneta, Y
Inoue, D
Matsumoto, T
Harigaya, K
Fujita, T
机构
[1] Univ Tokyo, Sch Med, Dept Med, Div Endocrinol & Nephrol, Tokyo 1138655, Japan
[2] Chiba Univ, Grad Sch Med, Dept Mol & Tumor Pathol, Chiba 2608670, Japan
[3] Univ Tokyo, Sch Med, Dept Lab Med, Tokyo 1138655, Japan
[4] Sankyo Co Ltd, Biomed Res Labs, Tokyo 140, Japan
[5] Univ Tokushima, Sch Med, Dept Internal Med 1, Tokushima 7708503, Japan
关键词
D O I
10.1074/jbc.M207804200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytokines in interleukin (IL)-11 subfamily participate in the regulation of bone cell proliferation and differentiation. We report here positive effects of IL-11 on osteoblasts and bone formation. Overexpression of human IL-11 gene in transgenic mice resulted in the stimulation of bone formation to increase cortical thickness and strength of long bones, and in the prevention of cortical bone loss with advancing age. Bone resorption and osteoclastogenesis were not affected in IL-11 transgenic mice. In experiments in vitro, IL-11 stimulated transcription of the target gene for bone morphogenetic protein (BMP) via STAT3, leading to osteoblastic differentiation in the presence of BMP-2, but inhibited adipogenesis in bone marrow stromal cells. These results indicate that IL-11 is a stimulatory factor for osteoblastogenesis and bone formation to conserve cortical bone, possibly by enhancing BMP actions in bone. IL-11 may be a new therapeutic target for senile osteoporosis.
引用
收藏
页码:49011 / 49018
页数:8
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