Zhao Yi, Jia Lingfei, Zheng Yunfei, Li Weiran
Department of Orthodontics, Peking University School and Hospital of Stomatology, Beijing 100081, China.
Department of Oral and Maxillofacial Surgery, Peking University School and Hospital of Stomatology, Beijing 100081, China.
Stem Cells Int. 2020 Aug 25;2020:4813140. doi: 10.1155/2020/4813140. eCollection 2020.
As the most important bone-resorbing cells, osteoclasts play fundamental roles in bone remodeling and skeletal health. Much effort has been focused on identifying the regulators of osteoclast metabolism. Noncoding RNAs (ncRNAs) reportedly regulate osteoclast formation, differentiation, survival, and bone-resorbing activity to participate in bone physiology and pathology. The present review intends to provide a general framework for how ncRNAs and their targets regulate osteoclast differentiation and the important events of osteoclastogenesis they are involved in, including osteoclast precursor generation, early differentiation, mononuclear osteoclast fusion, and multinucleated osteoclast function and survival. This framework is beneficial for understanding bone biology and for identifying the potential biomarkers or therapeutic targets of bone diseases. The review also summarizes the results of experiments and classic experiment methods for osteoclast-related researches.
作为最重要的骨吸收细胞,破骨细胞在骨重塑和骨骼健康中发挥着重要作用。人们致力于确定破骨细胞代谢的调节因子。据报道,非编码RNA(ncRNAs)可调节破骨细胞的形成、分化、存活和骨吸收活性,从而参与骨生理和病理过程。本综述旨在提供一个总体框架,说明ncRNAs及其靶标如何调节破骨细胞分化以及它们所参与的破骨细胞生成的重要事件,包括破骨细胞前体的产生、早期分化、单核破骨细胞融合以及多核破骨细胞的功能和存活。该框架有助于理解骨生物学,并有助于确定骨疾病的潜在生物标志物或治疗靶点。本综述还总结了破骨细胞相关研究的实验结果和经典实验方法。