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孤儿核受体ERRγ是肝细胞中CB1受体介导的TFR2基因表达的转录调节因子。

Orphan Nuclear Receptor ERRγ Is a Transcriptional Regulator of CB1 Receptor-Mediated TFR2 Gene Expression in Hepatocytes.

作者信息

Kim Bo-Eun, Choi Byungyoon, Park Woo-Ram, Kim Yu-Ji, Kim In-Young, Jung Yoon Seok, Kim Yong-Hoon, Lee Chul-Ho, Choi Hueng-Sik, Kim Don-Kyu

机构信息

Department of Integrative Food, Bioscience and Biotechnology, Chonnam National University, Gwangju 61186, Korea.

School of Biological Sciences and Technology, Chonnam National University, Gwangju 61186, Korea.

出版信息

Int J Mol Sci. 2021 Jun 2;22(11):6021. doi: 10.3390/ijms22116021.

DOI:10.3390/ijms22116021
PMID:34199599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8199698/
Abstract

Orphan nuclear receptor estrogen-related receptor γ (ERRγ) is an important transcription factor modulating gene transcription involved in endocrine control of liver metabolism. Transferrin receptor 2 (TFR2), a carrier protein for transferrin, is involved in hepatic iron overload in alcoholic liver disease (ALD). However, TFR2 gene transcriptional regulation in hepatocytes remains largely unknown. In this study, we described a detailed molecular mechanism of hepatic TFR2 gene expression involving ERRγ in response to an endocannabinoid 2-arachidonoylglycerol (2-AG). Treatment with 2-AG and arachidonyl-2'-chloroethylamide, a selective cannabinoid receptor type 1 (CB1) receptor agonist, increased ERRγ and TFR2 expression in hepatocytes. Overexpression of ERRγ was sufficient to induce TFR2 expression in both human and mouse hepatocytes. In addition, ERRγ knockdown significantly decreased 2-AG or alcohol-mediated TFR2 gene expression in cultured hepatocytes and mouse livers. Finally, deletion and mutation analysis of the TFR2 gene promoter demonstrated that ERRγ directly modulated TFR2 gene transcription via binding to an ERR-response element. This was further confirmed by chromatin immunoprecipitation assay. Taken together, these results reveal a previously unrecognized role of ERRγ in the transcriptional regulation of TFR2 gene expression in response to alcohol.

摘要

孤儿核受体雌激素相关受体γ(ERRγ)是一种重要的转录因子,可调节参与肝脏代谢内分泌控制的基因转录。转铁蛋白受体2(TFR2)是转铁蛋白的载体蛋白,参与酒精性肝病(ALD)中的肝脏铁过载。然而,肝细胞中转铁蛋白受体2(TFR2)基因的转录调控在很大程度上仍不清楚。在本研究中,我们描述了肝脏TFR2基因表达的详细分子机制,该机制涉及ERRγ对一种内源性大麻素2-花生四烯酸甘油酯(2-AG)的反应。用2-AG和花生四烯酰-2'-氯乙酰胺(一种选择性1型大麻素受体(CB1)激动剂)处理可增加肝细胞中ERRγ和TFR2的表达。ERRγ的过表达足以在人和小鼠肝细胞中诱导TFR2的表达。此外,ERRγ基因敲低显著降低了培养的肝细胞和小鼠肝脏中2-AG或酒精介导的TFR2基因表达。最后,对TFR2基因启动子的缺失和突变分析表明,ERRγ通过与ERR反应元件结合直接调节TFR2基因转录。染色质免疫沉淀试验进一步证实了这一点。综上所述,这些结果揭示了ERRγ在酒精应答下对TFR2基因表达转录调控中一个以前未被认识的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/d12ef546ee50/ijms-22-06021-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/1f24e1c8edc8/ijms-22-06021-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/6e6a00756f7f/ijms-22-06021-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/68708621cf70/ijms-22-06021-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/7c7098da2ed0/ijms-22-06021-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/0afbf405c7b2/ijms-22-06021-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/d12ef546ee50/ijms-22-06021-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/1f24e1c8edc8/ijms-22-06021-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/6e6a00756f7f/ijms-22-06021-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/68708621cf70/ijms-22-06021-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/7c7098da2ed0/ijms-22-06021-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/0afbf405c7b2/ijms-22-06021-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac49/8199698/d12ef546ee50/ijms-22-06021-g006.jpg

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