Angiopoietin-like 8 (ANGPTL8) expression is regulated by miR-143-3p in human hepatocytes

被引:18
作者
DiStefano, Johanna K. [1 ]
机构
[1] Translat Genom Res Inst, Diabet & Fibrot Dis Unit, 445 N 5th St, Phoenix, AZ 85004 USA
基金
美国国家卫生研究院;
关键词
microRNA; miRNA; miR-143-3p; Betatrophin; Angiopoietin-like protein 8; HDL-C; Inflammation; Hyperglycemia; Atherosclerosis; LIPID-METABOLISM; BETATROPHIN; ANGPTL8/BETATROPHIN; LIPOPROTEIN; LIPASIN; PROTEIN; FAT; IDENTIFICATION; DYSLIPIDEMIA; CHOLESTEROL;
D O I
10.1016/j.gene.2018.09.041
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Angiopoietin-like protein 8 (ANGPTL8) is associated with reduced HDL-cholesterol levels and may contribute to the development of dyslipidemia. Factors regulating ANGPTL8 expression remain poorly understood. Here we analyzed the relationship between miRNA-143-3p and ANGPTL8 in liver cells. Using target prediction algorithms, we identified a putative binding site for miR-143-3p in the ANGPTL8 3' untranslated region (3'UTR). Exogenous miR-143-3p interacted with the ANGPTL8 3'UTR to downregulate its expression compared to scrambled sequence control. Transfection of HepG2 cells with miR-143-3p mimic or siRNA resulted in decreased or increased ANGPTL8 transcript and protein levels, respectively. Treatment of HepG2 cells with 30 mM glucose, 100 nM insulin, or 75 ng/ml lipopolysaccharide to mimic hyperglycemic, hyperinsulinemic, and proinflammatory conditions corresponded with increased miR-143-3p and ANGPTL8 levels. Inhibition of miR-143-3p amplified ANGPTL8 response to these treatments, suggesting that the miRNA acts to suppress ANGPTL8 expression under metabolically distorted conditions. These results, combined with growing evidence supporting a role for ANGPTL8 in the regulation of HDL-C metabolism, provide a better understanding of the molecular mechanisms underlying ANGPTL8 expression.
引用
收藏
页码:1 / 6
页数:6
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