MicroRNA-425 controls lipogenesis and lipolysis in adipocytes

被引:38
作者
Qi, Renli [1 ,3 ]
Wang, Jing [1 ]
Wang, Qi [1 ]
Qiu, Xiaoyu [1 ]
Yang, Feiyun [3 ]
Liu, Zuohua [2 ]
Huang, Jinxiu [2 ]
机构
[1] Chongqing Acad Anim Sci, Rongchang 402460, Peoples R China
[2] Minist Agr, Key Lab Pig Ind Sci, Rongchang 402460, Peoples R China
[3] Chongqing Key Lab Pig Ind Sci, Rongchang 402460, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2019年 / 1864卷 / 05期
基金
国家重点研发计划;
关键词
MiR-425; Adipocyte; Mapk14; AMPK; Cab39; ADIPOGENIC TRANS-DIFFERENTIATION; PPAR-GAMMA; INHIBITION; ENERGY; PROLIFERATION; PROTEIN-1; TARGETS; BIOLOGY; MIR-27; BROWN;
D O I
10.1016/j.bbalip.2019.02.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An increasing number of studies have demonstrated that some microRNAs participate in the regulation of growth and development of adipocytes. The present study shows that microRNA-425-5p (miR-425) is a novel strong regulator of adipogenesis and adipolysis in adipocytes. Forced expression of miR-425 in mice promoted body fat accumulation and the development of obesity due to high-fat intake, whereas silencing miR-425 prevented mice from being obese. Mechanically, the expression of miR-425 is controlled by PPAR gamma during the adipogenesis process in adipocytes. MiR-425 overexpression resulted in a reduction in the proliferation of 3t3-L1 pre-adipocytes but significantly accelerated cellular adipogenic differentiation. Mapk14, a negative regulator of adipogenesis, was predicted and confirmed as a real target gene of miR-425. Moreover, knocking down miR-425 remarkably intensified intracellular lipolysis and promoted lipid oxidation, which is related to the activation of AMPK, a monitor for intracellular energy balance. MiR-425 activated AMPK not only by decreasing cellular ATP concentrations but also by targeting the gene of Cab39, which is an upstream co-activator of AMPK. The findings of the present study suggest that miR-425 could control adipogenesis and adipolysis in adipocytes by simultaneously triggering multidirectional targets.
引用
收藏
页码:744 / 755
页数:12
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