破骨细胞
骨吸收
细胞生物学
骨重建
化学
骨重建期
转基因小鼠
骨愈合
骨质疏松症
细胞内
信号转导
机制(生物学)
骨细胞
转基因
免疫学
医学
内科学
生物
生物化学
解剖
受体
哲学
认识论
基因
作者
Huaqiang Tao,Xuefeng Li,Qiufei Wang,Lei Yu,Yang Peng,Wenlong Chen,Xing Yang,Jun Zhou,Dechun Geng
标识
DOI:10.1016/j.freeradbiomed.2023.12.043
摘要
Bone remodeling is essential for the repair and replacement of damaged or aging bones. Continuous remodeling is necessary to prevent the accumulation of bone damage and to maintain bone strength and calcium balance. As bones age, the coupling mechanism between bone formation and absorption becomes dysregulated, and bone loss becomes dominant. Bone development and repair rely on interaction and communication between osteoclasts and surrounding cells. Osteoclasts are specialized cells that are accountable for bone resorption and degradation, and any abnormalities in their activity can result in notable alterations in bone structure and worsen disease symptoms. Recent findings from transgenic mouse models and bone analysis have greatly enhanced our understanding of the origin, differentiation pathway, and activation stages of osteoclasts. In this review, we explore osteoclasts and discuss the cellular and molecular events that drive their generation, focusing on intracellular oxidative and antioxidant signaling. This knowledge can help develop targeted therapies for diseases associated with osteoclast activation.
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