The osteoclast differentiation factor osteoprotegerin-ligand is essential for mammary gland development

被引:603
作者
Fata, JE
Kong, YY [1 ]
Li, J
Sasaki, T
Irie-Sasaki, J
Moorehead, RA
Elliott, R
Scully, S
Voura, EB
Lacey, DL
Boyle, WJ
Khokha, R
Penninger, JM
机构
[1] Pohang Univ Sci & Technol, Div Mol & Life Sci, Pohang 790784, Kyungbuk, South Korea
[2] Univ Toronto, Ontario Canc Inst, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
[3] Univ Toronto, Ontario Canc Inst, Dept Lab Med & Pathobiol, Toronto, ON M5G 2M9, Canada
[4] Univ Toronto, Ontario Canc Inst, Amgen Inst, Toronto, ON M5G 2C1, Canada
[5] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2C1, Canada
[6] Univ Toronto, Dept Immunol, Toronto, ON M5G 2C1, Canada
[7] Amgen Inc, Dept Cell Biol, Thousand Oaks, CA 91320 USA
[8] Amgen Inc, Dept Pathol, Thousand Oaks, CA 91320 USA
关键词
D O I
10.1016/S0092-8674(00)00103-3
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
Osteoprotegerin-ligand (OPGL) is a key osteoclast differentiation/activation factor essential for bone remodeling. We report that mice lacking OPGL or its receptor RANK fail to form lobulo-alveolar mammary structures during pregnancy, resulting in death of newborns. Transplantation and OPGL-rescue experiments in opgl(-/-) and rank(-/-) pregnant females showed that OPGL acts directly on RANK-expressing mammary epithelial cells. The effects of OPGL are autonomous to epithelial cells. The mammary gland defect in female opgl(-/-) mice is characterized by enhanced apoptosis and failures in proliferation and PKB activation in lobulo-alveolar buds that can be reversed by recombinant OPGL treatment. These data provide a novel paradigm in mammary gland development and an evolutionary rationale for hormonal regulation and gender bias of osteoporosis in females.
引用
收藏
页码:41 / 50
页数:10
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