Mizuno A, Amizuka N, Irie K, Murakami A, Fujise N, Kanno T, Sato Y, Nakagawa N, Yasuda H, Mochizuki S, Gomibuchi T, Yano K, Shima N, Washida N, Tsuda E, Morinaga T, Higashio K, Ozawa H
Research Institute of Life Science, Snow Brand Milk Products, Co., Ltd., Tochigi, Japan.
Biochem Biophys Res Commun. 1998 Jun 29;247(3):610-5. doi: 10.1006/bbrc.1998.8697.
Osteoclasts are multinucleated cells that resorb bone. Osteoclastogenesis inhibitory factor (OCIF), also called osteoprotegerin (OPG), acts as a naturally occurring decoy receptor for osteoclast differentiation factor, which mediates an essential signal to osteoclast progenitors for their differentiation into osteoclasts. Here we show that the OCIF/OPG knockout mice exhibited severe osteoporosis due to enhanced osteoclastogenesis when they grew to be adults. These mice were viable and fertile. They exhibited marked bone loss accompanied by destruction of growth plate and lack of trabecular bone in their femurs. The strength of their bones dramatically decreased. These results demonstrate that OCIF/OPG is a key factor acting as a negative regulator against osteoclastogenesis. The OCIF/OPG knockout mice provide the first animal model for osteoporosis without other obvious abnormalities.
破骨细胞是多核细胞,可吸收骨骼。破骨细胞生成抑制因子(OCIF),也称为骨保护素(OPG),作为破骨细胞分化因子的天然诱饵受体,介导对破骨细胞祖细胞分化为破骨细胞的重要信号。在此我们表明,OCIF/OPG基因敲除小鼠成年后由于破骨细胞生成增强而表现出严重的骨质疏松症。这些小鼠存活且可育。它们表现出明显的骨质流失,伴有生长板破坏和股骨小梁骨缺失。其骨骼强度显著降低。这些结果表明,OCIF/OPG是作为破骨细胞生成负调节因子的关键因素。OCIF/OPG基因敲除小鼠提供了首个无其他明显异常的骨质疏松症动物模型。