Department of Biotechnology, School of Bioengineering, SRM Institute of Science and Technology, Kattankulathur 603 203, Tamil Nadu, India.
Department of Biotechnology, School of Bioengineering, SRM Institute of Science and Technology, Kattankulathur 603 203, Tamil Nadu, India.
Life Sci. 2019 Sep 1;232:116676. doi: 10.1016/j.lfs.2019.116676. Epub 2019 Jul 21.
Bone is one of the most dynamic organs in the body that continuously undergoes remodeling through bone formation and resorption. A cascade of molecules and pathways results in the osteoblast differentiation that is attributed to osteogenesis, or bone formation. The process of osteogenesis is achieved through participation of the Wnt pathway, FGFs, BMPs/TGF-β, and transcription factors such as Runx2 and Osx. The activity and function of the master transcription factor, Runx2, is of utmost significance as it can induce the function of osteoblast differentiation markers. A number of microRNAs [miRNAs] have been recently identified in the regulation of Runx2 expression/activity, thus affecting the process of osteogenesis. miRNAs that target Runx2 corepressors favor osteogenesis, while miRNAs that target Runx2 coactivators inhibit osteogenesis. In this review, we focus on the regulation of Runx2 by miRNAs in osteoblast differentiation and their potential for treating bone and bone-related diseases.
骨骼是人体中最具活力的器官之一,通过骨形成和吸收不断进行重塑。一系列分子和途径导致成骨细胞分化,即骨生成。骨生成过程通过 Wnt 途径、FGFs、BMPs/TGF-β 和转录因子(如 Runx2 和 Osx)的参与来实现。主转录因子 Runx2 的活性和功能至关重要,因为它可以诱导成骨细胞分化标志物的功能。最近已经在 Runx2 表达/活性的调节中鉴定出许多 microRNAs [miRNAs],从而影响成骨过程。靶向 Runx2 核心抑制剂的 miRNAs 有利于成骨,而靶向 Runx2 共激活剂的 miRNAs 则抑制成骨。在这篇综述中,我们重点讨论了 miRNAs 对成骨细胞分化中 Runx2 的调节及其在治疗骨和骨相关疾病方面的潜力。