Angiogenic factor with G patch and FHA domains 1 (Aggf1) promotes hepatic steatosis in mice

被引:5
作者
Shao, Jing [1 ]
Zeng, Sheng [2 ]
Zhou, Bisheng [2 ]
Xu, Huihui [2 ]
Bian, Yaoyao [3 ]
Xu, Yong [2 ]
机构
[1] Nanjing Univ Chinese Med, Coll Basic Med Sci, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Pathophysiol, Key Lab Cardiovasc Dis & Mol Intervent, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Nursing, Nanjing, Jiangsu, Peoples R China
关键词
Aggf1; Steatosis; Hepatocyte; Insulin resistance; Gluconeogenesis; FATTY LIVER-DISEASE; TRANSCRIPTION FACTOR; NONALCOHOLIC STEATOHEPATITIS; INSULIN SENSITIVITY; FIBROSIS; INFLAMMATION; ACTIVATION; CELLS; INHIBITION; EXPRESSION;
D O I
10.1016/j.bbrc.2016.10.071
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Increased uptake of nutrients coupled with reduced activity leads to the development of a host of metabolic disorders in humans. In the present study we examined the role of angiogenic factor with G patch and FHA domains 1 (Aggf1) in the pathogenesis of steatosis, characterized by accumulation of lipids in the liver and consequently hepatic insulin resistance. We report here that Aggf1 expression was up-regulated in the liver in both genetically predisposed and diet-induced mouse model of steatosis. Aggf1 expression was also stimulated by free fatty acids in primary hepatocytes. Over-expression of Aggf1 in mice promoted steatosis. On the contrary, Aggf1 depletion ameliorated steatosis in mice. Mechanistically, Aggf1 activated the expression of gluconeogenesis gene and skewed the insulin signaling pathway to induce insulin resistance. Taken together, our data suggest that Aggf1 plays a role in steatosis in vivo and as such may be a new target in the development of therapeutics solutions against steatosis. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:134 / 140
页数:7
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