Identification of miR-26a as a Target Gene of Bile Acid Receptor GPBAR-1/TGR5

被引:14
作者
Chen, Xiaosong [1 ]
Xu, Haixia [2 ,3 ]
Ding, Lili [4 ]
Lou, Guiyu [4 ,5 ,6 ]
Liu, Yan [1 ]
Yao, Yalan [2 ,3 ]
Chen, Liangwan [1 ]
Huang, Wendong [4 ]
Fu, Xianghui [2 ,3 ]
机构
[1] Fujian Med Univ, Dept Plast Surg, Union Hosp, Fuzhou 350001, Fujian, Peoples R China
[2] Sichuan Univ, West China Hosp, Div Endocrinol & Metab, State Key Lab Biotherapy, Chengdu 610041, Sichuan, Peoples R China
[3] Collaborat Innovat Ctr Biotherapy, Chengdu 610041, Sichuan, Peoples R China
[4] City Hope Natl Med Ctr, Diabet & Metab Res Inst, Beckman Res Inst, Dept Diabet Complicat & Metab, Duarte, CA 91010 USA
[5] Henan Peoples Hosp, Cent Lab, Zhengzhou 450003, Henan, Peoples R China
[6] Zhengzhou Univ, Peoples Hosp, Zhengzhou 450003, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
TGR5; METABOLISM; MICRORNAS; PROTECTS; GLUCOSE; CELLS; LIVER;
D O I
10.1371/journal.pone.0131294
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
GPBAR1/TGR5 is a G protein-coupled receptor of bile acids. TGR5 is known to regulate the BA homeostasis and energy metabolism. Recent studies highlight an important role of TGR5 in alleviating obesity and improving glucose regulation, however, the mechanism of which is still unclear. Here we report that TGR5 is involved in mediating the anti-obesity and anti-hyperglycemia effect of a natural compound, oleanolic acid. By comparing the miRNA profiles between wild type and TGR5(-/-) livers after OA treatment, we identified miR-26a as a novel downstream target gene of TGR5 activation. The expression of miR-26a in the liver was induced in a TGR5-dependent manner after feeding the mice with a bile acid diet. TGR5 activation strongly increased the expression of miR-26a in macrophages, including the Kupffer cells in the liver. We further demonstrated that JNK pathway was required for miR-26a induction by TGR5 activation. Interestingly, we located the TGR5-responsive DNA element to a proximal region of miR-26's promoter, which was independent of the transcription of its host genes. These results unravel a new mechanism by which bile acid receptor TGR5 activates a miRNA gene expression.
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页数:12
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