成骨细胞
瘦素
生物
骨质疏松症
骨重建
骨形成
转录因子
细胞生物学
激素
细胞分化
生物信息学
计算生物学
内分泌学
遗传学
基因
肥胖
体外
作者
Patricia Ducy,Thorsten Schinke,Gérard Karsenty
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2000-09-01
卷期号:289 (5484): 1501-1504
被引量:1115
标识
DOI:10.1126/science.289.5484.1501
摘要
The study of the biology of osteoblasts, or bone-forming cells, illustrates how mammalian genetics has profoundly modified our understanding of cell differentiation and physiologic processes. Indeed, genetic-based studies over the past 5 years have revealed how osteoblast differentiation is controlled through growth and transcription factors. Likewise, the recent identification, using mutant mouse models, of a central component in the regulation of bone formation expands our understanding of the control of bone remodeling. This regulatory loop, which involves the hormone leptin, may help to explain the protective effect of obesity on bone mass in humans. In addition, it provides a novel physiologic concept that may shed light on the etiology of osteoporosis and help to identify new therapeutic targets.
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