Orphan nuclear receptor ERRγ is a transcriptional regulator of CB1 receptor-mediated TFR2 gene expression in hepatocytes

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dc.contributor.authorB E Kim-
dc.contributor.authorB Choi-
dc.contributor.authorW R Park-
dc.contributor.authorY J Kim-
dc.contributor.authorI Y Kim-
dc.contributor.authorY S Jung-
dc.contributor.authorYong-Hoon Kim-
dc.contributor.authorChul-Ho Lee-
dc.contributor.authorH S Choi-
dc.contributor.authorD K Kim-
dc.date.accessioned2021-06-09T03:30:58Z-
dc.date.available2021-06-09T03:30:58Z-
dc.date.issued2021-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/24386-
dc.description.abstractOrphan 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.-
dc.publisherMDPI-
dc.titleOrphan nuclear receptor ERRγ is a transcriptional regulator of CB1 receptor-mediated TFR2 gene expression in hepatocytes-
dc.title.alternativeOrphan nuclear receptor ERRγ is a transcriptional regulator of CB1 receptor-mediated TFR2 gene expression in hepatocytes-
dc.typeArticle-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.number11-
dc.citation.endPage6021-
dc.citation.startPage6021-
dc.citation.volume22-
dc.contributor.affiliatedAuthorYong-Hoon Kim-
dc.contributor.affiliatedAuthorChul-Ho Lee-
dc.contributor.alternativeName김보은-
dc.contributor.alternativeName최병윤-
dc.contributor.alternativeName박우람-
dc.contributor.alternativeName김유지-
dc.contributor.alternativeName김인영-
dc.contributor.alternativeName정윤석-
dc.contributor.alternativeName김용훈-
dc.contributor.alternativeName이철호-
dc.contributor.alternativeName최흥식-
dc.contributor.alternativeName김돈규-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, vol. 22, no. 11, pp. 6021-6021-
dc.identifier.doi10.3390/ijms22116021-
dc.subject.keywordEstrogen-related receptor γ (ERRγ)-
dc.subject.keywordTransferrin receptor 2 (TFR2)-
dc.subject.keywordCannabinoid receptor type 1 (CB1)-
dc.subject.keywordOrphan nuclear receptor-
dc.subject.keywordgene regulation-
dc.subject.keyword2-AG-
dc.subject.keywordHepatic iron overload-
dc.subject.keywordAlcoholic liver disease-
dc.subject.localEstrogen-related receptor γ (ERRγ)-
dc.subject.localestrogen-related receptor γ (ERRγ)-
dc.subject.localEstrogen-related receptor γ-
dc.subject.localTransferrin receptor 2 (TFR2)-
dc.subject.localCannabinoid receptor type 1 (CB1)-
dc.subject.localOrphan nuclear receptor-
dc.subject.localORPHAN NUCLEAR RECEPTOR-
dc.subject.localorphan nuclear receptors-
dc.subject.localgene regulation-
dc.subject.localGene regulation-
dc.subject.local2-AG-
dc.subject.localHepatic iron overload-
dc.subject.localalcoholic liver disease-
dc.subject.localAlcoholic liver disease-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Laboratory Animal Resource & Research Center > 1. Journal Articles
Ochang Branch Institute > Division of National Bio-Infrastructure > 1. Journal Articles
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