PPARγ regulates PNPLA3 in adipocytes in vitro and in vivo in healthy obese patients and mice with metabolic dysfunction-associated steatohepatitis

Author:

Dixon Emmanuel1,Claudel Thierry1,White Ursula2,Zimmermann Robert3,Haemmerle Guenter3,Wabitsch Martin4,Mlitz Veronika1,Fuchs-Steiner Claudia1,Ravussin Eric2,Trauner Michael1

Affiliation:

1. Hans Popper Laboratory of Molecular Hepatology, Division of Gastroenterology and Hepatology, Medical University of Vienna

2. Pennington Biomedical Research Center

3. University of Graz

4. Ulm University Medical Center

Abstract

Abstract

The mechanisms regulating the patatin-like phospholipase domain-containing protein 3 (PNPLA3) are currently unclear. We uncovered that peroxisome proliferator-activated receptor gamma (PPARγ) transcriptionally regulates PNPLA3 in vitro and in vivo in humans and diabetic and hyperlipidaemic mice. We observed increased PNPLA3 mRNA transcripts in the subcutaneous femoral but not in the abdominal fat of healthy women with obesity who received 30 mg/day of pioglitazone over 16 weeks in “The Apple & Pear trial (“Cellular Dynamics of Subcutaneous Fat Distribution in Obese Women”; ClinicalTrials.gov ID- NCT01748994)”. Likewise, pioglitazone treatment upregulated Pnpla3 in adipose tissue but not the liver of the STAM mice with metabolic dysfunction-associated steatohepatitis. Since pioglitazone has a moderate effect on human PPARγ, we used the most potent PPARγ agonist, rosiglitazone, to show that PPARγ regulation of PNPLA3 involves a direct transcriptional mechanism. Mechanistically, we further interrogated the interaction between PNPLA3 and PPARγ using in silico analysis, luciferase reporter assay, gene expression analysis, and gel shift assays. Rosiglitazone increased luciferase activity in PNPLA3 and PPARγ co-transfected cells, demonstrating PPARγ-mediated induction of PNPLA3 promoter activity. Unexpectedly, we identified two binding sites (PPREs), bp -713 to -707 and bp -790 to -780, in the PNPLA3 promoter recognized by PPARγ. Mutation in these newly identified sites abolishes the PPARγ-mediated induction and binding activities. Collectively, these results establish a novel role of PPARγ in PNPLA3 gene regulation.

Publisher

Springer Science and Business Media LLC

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3