Department of Stomatology, Jin Ling Hospital (Nanjing General Hospital of Nanjing Military Command), Medical School of Nanjing University, Nanjing, Jiangsu 210002, People's Republic of China.
Department of Stomatology, PLA Army General Hospital, Beijing 100000, People's Republic of China.
Life Sci. 2019 Mar 1;220:84-91. doi: 10.1016/j.lfs.2019.01.051. Epub 2019 Jan 30.
A number of evidences suggest that microRNAs are involved in the adipogenic commitment of mesenchymal stem cells (MSCs). Recent studies have investigated that miR-199a-3p played a pivotal role in adipocyte differentiation. However, the detailed mechanism in this complex biological process remains largely unknown. In current study, we found that the expression of miR-199a-3p was gradually increased during adipogenic differentiation of bone marrow derived mesenchymal stem cells (BMMSCs). Enhanced expression of miR-199a-3p promoted adipogenesis, whereas silence of miR-199a-3p rescued BMMSCs from adipogenic commitment. For further mechanism exploration, KDM6A was confirmed to be the target of miR-199a-3p and the expression of KDM6A was gradually decreased during adipogenic differentiation of BMMSCs. Furthermore, up-regulation of KDM6A markedly abolished the miR-199a-3p overexpression induced adipogenic augmentation, whereas down-regulation of KDM6A suppressed the adipogenic reduction caused by miR-199a-3p silence. In addition, WNT signaling was also verified to be the downstream of miR-199a-3p/KDM6A to regulate adipogenic differentiation of BMMSCs. Taken together, current results indicate that miR-199a-3p regulate adipogenesis of BMMSCs by targeting KDM6A/WNT signaling, which highlights a new insight for a better understanding of molecular mechanism and stem cell based therapy on osteoporotic diseases.
有许多证据表明 microRNAs 参与了间充质干细胞(MSCs)的脂肪生成。最近的研究表明 miR-199a-3p 在脂肪细胞分化中发挥关键作用。然而,这个复杂的生物学过程中的详细机制在很大程度上仍然未知。在本研究中,我们发现 miR-199a-3p 的表达在骨髓间充质干细胞(BMMSCs)的脂肪生成分化过程中逐渐增加。增强 miR-199a-3p 的表达促进了脂肪生成,而沉默 miR-199a-3p 则阻止了 BMMSCs 的脂肪生成。为了进一步探索机制,我们证实 KDM6A 是 miR-199a-3p 的靶基因,并且 KDM6A 的表达在 BMMSCs 的脂肪生成分化过程中逐渐降低。此外,上调 KDM6A 显著消除了 miR-199a-3p 过表达诱导的脂肪生成增强,而下调 KDM6A 则抑制了由 miR-199a-3p 沉默引起的脂肪生成减少。此外,WNT 信号也被证实是 miR-199a-3p/KDM6A 的下游靶点,以调节 BMMSCs 的脂肪生成。总之,目前的结果表明,miR-199a-3p 通过靶向 KDM6A/WNT 信号调节 BMMSCs 的脂肪生成,这为更好地理解骨质疏松症的分子机制和基于干细胞的治疗提供了新的见解。