脂联素
安普克
脂联素受体1
过氧化物酶体增殖物激活受体
内分泌学
内科学
基因敲除
受体
肝X受体
载脂蛋白B
化学
核受体
脂肪组织
生物
蛋白激酶A
转录因子
细胞生物学
激酶
基因
医学
胰岛素抵抗
胆固醇
糖尿病
生物化学
作者
D. A. Tanyanskiy,Vladimir S. Shavva,Dizhe Eb,Galina N. Oleinikova,А. В. Лизунов,Ekaterina V. Nekrasova,Denis A. Mogilenko,Ekaterina E. Larionova,Sergey Orlov,A.D. Denisenko
出处
期刊:Biokhimiya
[Pleiades Publishing]
日期:2022-11-01
卷期号:87 (11): 1252-1259
被引量:9
标识
DOI:10.1134/s0006297922110049
摘要
Adiponectin is an adipose tissue hormone, participating in energy metabolism and involved in atherogenesis. Previously, it was found that adiponectin increases expression of the APOA1 (apolipoprotein A-1) gene in hepatocytes, but the mechanisms of this effect remained unexplored. Our aim was to investigate the role of adiponectin receptors AdipoR1/R2, AMP-activated protein kinase (AMPK), nuclear peroxisome proliferator-activated receptor alpha (PPARα) and liver X receptors (LXRs) in mediating the action of adiponectin on hepatic APOA1 expression in human hepatoma HepG2 cells. The level of APOA1 expression was determined by RT-qPCR and ELISA. We showed that the siRNA-mediated knockdown of genes coding for AdipoR1, AdipoR2, AMPK, PPARα, and LXRα and β prevented adiponectin-induced APOA1 expression in HepG2 cells and demonstrated that interaction of PPARα and LXRs with the APOA1 gene hepatic enhancer is important for the adiponectin-dependent APOA1 transcription. The results of this study point out to the involvement of both types of adiponectin receptors, AMPK, PPARα, and LXRs in the adiponectin-dependent upregulation of the APOA1 expression.
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