成骨细胞
破骨细胞
骨细胞
甲状旁腺激素
骨重建期
骨重建
细胞凋亡
骨质疏松症
细胞生物学
内科学
内分泌学
激素
化学
癌症研究
生物
医学
体外
钙
受体
生物化学
作者
Lianping Xing,Brendan F. Boyce
标识
DOI:10.1016/j.bbrc.2004.11.072
摘要
In postnatal life, the skeleton undergoes continuous remodeling in which osteoclasts resorb aged or damaged bone, leaving space for osteoblasts to make new bone. The balance of proliferation, differentiation, and apoptosis of bone cells determines the size of osteoclast or osteoblast populations at any given time. Bone cells constantly receive signals from adjacent cells, hormones, and bone matrix that regulate their proliferation, activity, and survival. Thus, the amount of bone and its microarchitecture before and after the menopause or following therapeutic intervention with drugs, such as sex hormones, glucocorticoids , parathyroid hormone , and bisphosphonates, is determined in part by effects of these on survival of osteoclasts, osteoblasts, and osteocytes . Understanding the mechanisms and regulation of bone cell apoptosis will enhance our knowledge of bone cell function and help us to develop better therapeutics for the management of osteoporosis and other bone diseases.
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