Vitamin C Inhibits the Metabolic Changes Induced by Tet1 Insufficiency Under High Fat Diet Stress. Issue 16 (23rd June 2021)

• Record Type: Journal Article
• Authors: Yuan, Yangmian; Liu, Chengyu; Chen, Xingrui; Sun, Yuyan; Xiong, Mingrui; Fan, Yu; Petersen, Robert B.; Chen, Hong; Huang, Kun; Zheng, Ling
• Is Part Of: Molecular nutrition & food research. Volume 65:Issue 16(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-06-23
• Subjects: DNA methylation -- lipid metabolism -- obesity -- Tet1 -- vitamin C; Food -- Biotechnology -- Periodicals; Food -- Microbiology -- Periodicals; Nutrition -- Periodicals; Food -- Toxicology -- Periodicals; Nutrition -- Periodicals; Food Microbiology -- Periodicals; Food Technology -- Periodicals; Molecular Biology -- Periodicals; 664.0705
• DOI: 10.1002/mnfr.202100417
• Languages: English
• ISSNs: 1613-4125

Abstract

Abstract : Scope: DNA methylation contributes to obesity, but the role of the DNA demethylase ten‐eleven translocation protein 1 (Tet1) in obesity remains unclear. Vitamin C is a cofactor for the Tet family of proteins, but whether vitamin C can be used to treat obesity via Tet1 awaits clarification. Methods and Results: Tet1 +/+ and Tet1 +/− mice are fed a high fat diet (HFD). Higher weight gain and more severe hepatic steatosis, accompanied by reduced 5‐hydromethylcytosine (5hmC) levels, are found in the white adipose tissue and liver of Tet1 +/− mice. Accumulated lipids are observed in palmitic acid or oleic acid treated primary hepatocytes derived from Tet1 +/− mice, which are rescued by Tet1 overexpression or vitamin C treatment. Bisulfite sequencing reveals higher DNA methylation levels on lipolysis related genes in the liver of Tet1 +/− mice. Notably, oral intake of vitamin C normalizes DNA methylation levels, promotes lipolysis, and decreases obesity in HFD‐fed Tet1 +/− mice. Conclusions: The results reveal a novel function of Tet1 in obesity and provide a new mechanism for the beneficial role of vitamin C in metabolic diseases through enhanced Tet1 activity. Abstract : The study finds that Tet1 haplo‐insufficient ( Tet1 +/− ) mice show an obese‐prone phenotype, accompanied by severer glucose intolerance, and hepatic steatosis under HFD‐fed conditions. Vitamin C reduces fat mass, alleviates glucose intolerance, and hepatic steatosis of HFD‐fed Tet1 +/− mice through regulating Tet1's activity. Specifically, vitamin C prevents Tet1 insufficiency‐caused lipid accumulation associated with methylation of promoters of Hsl and Ppara genes.