牙槽
骨重建
成骨细胞
条件基因敲除
STAT蛋白
车站3
基因剔除小鼠
细胞生物学
化学
病理
解剖
医学
表型
生物
信号转导
牙科
内科学
受体
体外
生物化学
基因
作者
Yuanqi Liu,Siyuan Sun,Ziyi Jiang,Xinyi Gong,Yiling Yang,Yanfei Zhu,Hongyuan Xu,Anting Jin,Xiangru Huang,Xin Gao,Tingwei Lu,Jingyi Liu,Xinyu Wang,Qinggang Dai,Lingyong Jiang
摘要
The alveolar bone, with a high turnover rate, is the most actively-remodeling bone in the body. Orthodontic tooth movement (OTM) is a common artificial process of alveolar bone remodeling in response to mechanical force, but the underlying mechanism remains elusive. Previous studies have been unable to reveal the precise mechanism of bone remodeling in any time and space due to animal model-related restrictions. The signal transducer and activator of transcription 3 (STAT3) is important in bone metabolism, but its role in osteoblasts during OTM is unclear. To provide in vivo evidence that STAT3 participates in OTM at specific time points and in particular cells during OTM, we generated a tamoxifen-inducible osteoblast lineage-specific Stat3 knockout mouse model, applied orthodontic force, and analyzed the alveolar bone phenotype. Micro-computed tomography (Micro-CT) and stereo microscopy were used to access OTM distance. Histological analysis selected the area located within three roots of the first molar (M1) in the cross-section of the maxillary bone as the region of interest (ROI) to evaluate the metabolic activity of osteoblasts and osteoclasts, indicating the effect of orthodontic force on alveolar bone. In short, we provide a protocol for using inducible osteoblast lineage-specific Stat3 knockout mice to study bone remodeling under orthodontic force and describe methods for analyzing alveolar bone remodeling during OTM, thus shedding new light on skeletal mechanical biology.
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