MicroRNA miR-7 and miR-17-92 in the Arcuate Nucleus of Mouse Hypothalamus Regulate Sex-Specific Diet-Induced Obesity

被引:20
作者
Gao, Yanxia [1 ]
Li, Jiaheng [2 ,3 ]
Zhang, Zhen [1 ]
Zhang, Ruihan [4 ]
Pollock, Andrew [5 ]
Sun, Tao [2 ,3 ,5 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Shanghai 200240, Peoples R China
[2] Huaqiao Univ, Sch Med, Ctr Precis Med, Xiamen 361021, Fujian, Peoples R China
[3] Huaqiao Univ, Sch Biomed Sci, Xiamen 361021, Fujian, Peoples R China
[4] Shanghai Jiao Tong Univ, Zhiyuan Coll, Shanghai 200240, Peoples R China
[5] Cornell Univ, Weill Med Coll, Dept Cell & Dev Biol, 1300 York Ave, New York, NY 10065 USA
基金
中国国家自然科学基金;
关键词
miR-7; miR-17-92; Obesity; POMC neurons; Sex-differential gene; NEURAL STEM-CELL; POMC NEURONS; GLUCOSE-HOMEOSTASIS; LEPTIN; FOXA1; CLUSTER; RECOGNITION; EXPRESSION; ANXIETY; TARGET;
D O I
10.1007/s12035-019-1618-y
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Proper appetite, energy expenditure, and glucose and fat metabolisms are regulated by neurons in the arcuate nucleus (ARC) of mammalian hypothalamus. Studies have shown sex-specific difference in diet-induced obesity, but the underlying mechanisms remain unclear. Here, we show that microRNA (miRNA) miR-7 and miR-17-92 are expressed in proopiomelanocortin (POMC)-expressing neurons in the mouse ARC. Specific knockdown of miR-7 and knockout of miR-17-92 in POMC-expressing neurons aggravate diet-induced obesity only in females and males, respectively. Sex-differentially expressed genes are identified in the male and female ARC of wild-type adult mice using RNA sequencing. Interestingly, some target genes for miR-7 and miR-17-92 not only display sex-differential expression in the male and female ARC but also respond to high-fat diet treatment in miR-7 knockdown and miR-17-92 knockout mice. Our results demonstrate an important role of miRNAs in regulating sex-specific diet-induced obesity, likely through modulating expression of target genes that show sex-differential expression in the ARC of the hypothalamus.
引用
收藏
页码:7508 / 7521
页数:14
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