Inoue Kazuki, Ng Courtney, Xia Yuhan, Zhao Baohong
Arthritis and Tissue Degeneration Program, David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, NY, United States.
Department of Medicine, Weill Cornell Medicine, New York, NY, United States.
Front Cell Dev Biol. 2021 Jun 18;9:651161. doi: 10.3389/fcell.2021.651161. eCollection 2021.
Osteoclasts are specialized bone-resorbing cells that contribute to physiological bone development and remodeling in bone metabolism throughout life. Abnormal production and activation of osteoclasts lead to excessive bone resorption in pathological conditions, such as in osteoporosis and in arthritic diseases with bone destruction. Recent epigenetic studies have shed novel insight into the dogma of the regulation of gene expression. microRNAs belong to a category of epigenetic regulators, which post-transcriptionally regulate and silence target gene expression, and thereby control a variety of biological events. In this review, we discuss miRNA biogenesis, the mechanisms utilized by miRNAs, several miRNAs that play important roles in osteoclast differentiation, function, survival and osteoblast-to-osteoclast communication, and their translational potential and challenges in bone biology and skeletal diseases.
破骨细胞是专门负责骨吸收的细胞,在整个生命过程中的骨代谢中对生理性骨发育和重塑发挥作用。破骨细胞的异常产生和激活会导致在病理状态下骨吸收过度,如在骨质疏松症以及伴有骨破坏的关节炎疾病中。最近的表观遗传学研究为基因表达调控的理论带来了新的见解。微小RNA属于一类表观遗传调节因子,它们在转录后调节并使靶基因表达沉默,从而控制各种生物学事件。在本综述中,我们讨论了微小RNA的生物合成、微小RNA所利用的机制、在破骨细胞分化、功能、存活以及成骨细胞与破骨细胞通讯中发挥重要作用的几种微小RNA,以及它们在骨生物学和骨骼疾病中的转化潜力与挑战。