Estrogen Inhibits Bone Resorption by Directly Inducing Apoptosis of the Bone-resorbing Osteoclasts

Author:

Kameda Takashi1,Mano Hiroshi1,Yuasa Tatsuhisa1,Mori Yoshihisa1,Miyazawa Koshi1,Shiokawa Miho1,Nakamaru Yukiya1,Hiroi Emi1,Hiura Kenji1,Kameda Akira1,Yang Na N.1,Hakeda Yoshiyuki1,Kumegawa Masayoshi1

Affiliation:

1. From the Department of Orthodontics, Nippon Dental University School of Dentistry at Niigata, Niigata 951, Japan; Department of Oral Anatomy, Meikai University School of Dentistry, Sakado, Saitama 350-02, Japan; and Endocrine Research, Eli Lilly & Co., Indianapolis, Indiana 46285

Abstract

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 β-estradiol (E2) was able to directly inhibit osteoclastic bone resorption. At concentrations effective for inhibiting bone resorption, E2 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 E2 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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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