Estrogen inhibits bone resorption by directly inducing apoptosis of the bone-resorbing osteoclasts

被引:363
作者
Kameda, T
Mano, H
Yuasa, T
Mori, Y
Miyazawa, K
Shiokawa, M
Nakamaru, Y
Hiroi, E
Hiura, K
Kameda, A
Yang, NN
Hakeda, Y
Kumegawa, M
机构
[1] MEIKAI UNIV,SCH DENT,DEPT ORAL ANAT,SAKADO,SAITAMA 35002,JAPAN
[2] NIPPON DENT UNIV,SCH DENT,DEPT ORTHODONT,NIIGATA 951,JAPAN
[3] ELI LILLY & CO,INDIANAPOLIS,IN 46285
关键词
D O I
10.1084/jem.186.4.489
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Estrogen deficiency causes bone loss, which can be prevented by estrogen replacement therapy. Using a recently developed technique for isolation of highly purified mammalian osteoclasts, we showed that 17 beta-estradiol (E-2) was able to directly inhibit osteoclastic bone resorption. At concentrations effective for inhibiting bone resorption, E-2 also directly induced osteoclast apoptosis in a dose-and time-dependent manner. ICI164,384 and tamoxifen, as pure and partial antagonists, respectively, completely or partially blocked the effect of E-2 on both inhibition of osteoclastic bone resorption and induction of osteoclast apoptosis. These data suggest that the protective effects of estrogen against postmenopausal osteoporosis are mediated in part by the direct induction of apoptosis of the bone-resorbing osteoclasts by an estrogen receptor-mediated mechanism.
引用
收藏
页码:489 / 495
页数:7
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