4.7 Article

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

期刊

出版社

MDPI
DOI: 10.3390/ijms22116021

关键词

estrogen-related receptor gamma (ERR gamma); transferrin receptor 2 (TFR2); cannabinoid receptor type 1 (CB1); orphan nuclear receptor; gene regulation; 2-AG; hepatic iron overload; alcoholic liver disease

资金

  1. National Research Foundation of Korea (NRF) - Korea government (MSIT) [NRF-2018R1D1A1B07043953, 2021R1A2C1011136, NRF-2021R1A2C3004923, 2021R1A6A3A13038592 toW.-R.P., 2021R1A6A3A13038581]
  2. National Research Foundation of Korea [2021R1A6A3A13038581, 2021R1A2C1011136] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

This study elucidated the detailed molecular mechanism of hepatic TFR2 gene expression involving ERR gamma in response to the endocannabinoid 2-arachidonoylglycerol (2-AG). The results showed that ERR gamma overexpression was sufficient to induce TFR2 expression, while ERR gamma knockdown significantly decreased 2-AG or alcohol-mediated TFR2 gene expression. These findings reveal a previously unrecognized role of ERR gamma in the transcriptional regulation of TFR2 gene expression in response to alcohol.
Orphan nuclear receptor estrogen-related receptor gamma (ERR gamma) 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 ERR gamma 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 ERR gamma and TFR2 expression in hepatocytes. Overexpression of ERR gamma was sufficient to induce TFR2 expression in both human and mouse hepatocytes. In addition, ERR gamma 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 ERR gamma 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 ERR gamma in the transcriptional regulation of TFR2 gene expression in response to alcohol.

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