Zhou Jie, Yang Junying, Wang Xiaochen, Li Mengyue, Li Fang, Zhu Endong, Li Xuemei, Li Xiaoxia, Wang Baoli
NHC Key Lab of Hormones and Development, Tianjin Key Lab of Metabolic Diseases, Chu Hsien-I Memorial Hospital & Institute of Endocrinology, Tianjin Medical University, Tianjin, China.
Department of Microbiology, College of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Front Endocrinol (Lausanne). 2020 Jan 8;10:894. doi: 10.3389/fendo.2019.00894. eCollection 2019.
Recent studies have identified growing importance of microRNAs as key regulators of adipocyte differentiation. We have previously reported that miR-20a-5p is able to induce adipogenesis of established adipogenic cell lines and bone marrow derived mesenchymal stem cells (BMSCs). However, the molecular mechanisms by which miR-20a-5p controls adipogenesis and by which miR-20a-5p expression is regulated need to be further explored. In the current study we found that miR-20a-5p expression was induced during adipocyte differentiation from preadipocyte 3T3-L1 and was increased in epididymal white adipose tissue from either ob/ob mice or high fat diet-induced obese mice. Functional studies identified miR-20a-5p as a positive regulator of adipocyte differentiation and lipogenesis in 3T3-L1 by using either synthetic mimics to supplement miR-20a-5p, or using synthetic inhibitor or sponge lentivirus to inactivate endogenous miR-20a-5p. Luciferase activity assay revealed that TOB2 is a novel target of miR-20a-5p and functional experiment demonstrated its negative regulatory role in adipocyte differentiation. Moreover, Tob2 overexpression significantly attenuated adipocyte formation induced by miR-20a-5p supplementation. In-depth investigation of mechanisms that govern miR-20a-5p expression clarified that C/EBPα transcriptionally activated miR-20a-5p expression via binding to the promoter of miR-20a-5p. Taken together, we conclude that a novel C/EBPα/miR-20a-5p/TOB2 circuit exists and regulates adipogenesis and lipogenesis.
最近的研究表明,微小RNA作为脂肪细胞分化的关键调节因子,其重要性日益凸显。我们之前曾报道,miR-20a-5p能够诱导已建立的脂肪生成细胞系和骨髓来源的间充质干细胞(BMSC)发生脂肪生成。然而,miR-20a-5p控制脂肪生成的分子机制以及miR-20a-5p表达的调控机制仍有待进一步探索。在本研究中,我们发现miR-20a-5p的表达在脂肪前体细胞3T3-L1向脂肪细胞分化的过程中被诱导,并且在ob/ob小鼠或高脂饮食诱导的肥胖小鼠的附睾白色脂肪组织中增加。功能研究通过使用合成模拟物补充miR-20a-5p,或使用合成抑制剂或海绵慢病毒使内源性miR-20a-5p失活,确定miR-20a-5p是3T3-L1中脂肪细胞分化和脂肪生成的正调节因子。荧光素酶活性测定显示TOB2是miR-20a-5p的一个新靶点,功能实验证明其在脂肪细胞分化中起负调节作用。此外,Tob2的过表达显著减弱了miR-20a-5p补充诱导的脂肪细胞形成。对调控miR-20a-5p表达机制的深入研究表明,C/EBPα通过与miR-20a-5p的启动子结合,转录激活miR-20a-5p的表达。综上所述,我们得出结论,存在一个新的C/EBPα/miR-20a-5p/TOB2回路,该回路调节脂肪生成和脂肪形成。