破骨细胞
骨吸收
吸收
细胞生物学
骨质疏松症
骨重建期
化学
骨重建
内科学
巨噬细胞集落刺激因子
骨免疫学
骨保护素
兰克尔
巨噬细胞
骨质疏松症
内分泌学
生物
医学
受体
生物化学
激活剂(遗传学)
体外
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2000-09-01
卷期号:289 (5484): 1504-1508
被引量:3780
标识
DOI:10.1126/science.289.5484.1504
摘要
Osteoporosis, a disease endemic in Western society, typically reflects an imbalance in skeletal turnover so that bone resorption exceeds bone formation. Bone resorption is the unique function of the osteoclast, and anti-osteoporosis therapy to date has targeted this cell. The osteoclast is a specialized macrophage polykaryon whose differentiation is principally regulated by macrophage colony-stimulating factor, RANK ligand, and osteoprotegerin. Reflecting integrin-mediated signals, the osteoclast develops a specialized cytoskeleton that permits it to establish an isolated microenvironment between itself and bone, wherein matrix degradation occurs by a process involving proton transport. Osteopetrotic mutants have provided a wealth of information about the genes that regulate the differentiation of osteoclasts and their capacity to resorb bone.
科研通智能强力驱动
Strongly Powered by AbleSci AI