Mechanism of O-GlcNAcylation regulating liver lipid synthesis in mice through FASN

被引:0
|
作者
Li, Xiaoshuang [1 ]
Zhang, Ziyang [1 ]
Zhang, Meng [1 ,2 ]
Cao, Yu [1 ,3 ]
Zhou, Wanhui [1 ]
Kou, Lele [1 ]
Guo, Wenjin [2 ]
Zhang, Boxi [1 ]
Li, Shize [1 ]
Xu, Bin [1 ]
机构
[1] Heilongjiang Bayi Agr Univ, Coll Anim Sci & Vet Med, Daqing 163319, Peoples R China
[2] Jilin Univ, Coll Anim Sci & Vet Med, Changchun, Peoples R China
[3] Heilongjiang Acad Agr Sci, Branch Anim Husb & Vet Branch, Qiqihar, Heilongjiang, Peoples R China
来源
FASEB JOURNAL | 2025年 / 39卷 / 04期
基金
中国国家自然科学基金;
关键词
fatty acid synthase; liver lipid synthesis; mice; O-GlcNAcylation; ubiquitination;
D O I
10.1096/fj.202402451RR
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nonalcoholic fatty liver disease (NAFLD) has become one of the most common chronic liver diseases. O-Linked attachment of beta-N-acetylglucosamine (O-GlcNAc) are ubiquitous post-translational modifications of proteins as "nutrient sensors" and "stress receptors" in the body that are involved in maintaining normal cellular physiological functions. Increased levels of O-GlcNAcylation have been found in the liver samples of patients with NAFLD and nonalcoholic steatohepatitis. However, the role of O-GlcNAcylation in the development and pathogenesis of NAFLD remains unclear. Here, we sought to determine the specific role of O-GlcNAcylation in NAFLD. In this study, the results demonstrated that inhibition of O-GlcNAc transferase (OGT) led to decreased expression of liver lipid synthesis genes and proteins in vitro. In addition, we showed that fatty acid synthase (FASN) expression was positively correlated with O-GlcNAcylation levels. Immunoprecipitation and pulldown assays confirmed the interaction between FASN and OGT at the serine 1483 of FASN, to inhibit K48-linked ubiquitination and degradation of FASN, thereby promoting hepatic lipid accumulation and the development of NAFLD. Administration of the OGT inhibitor OSMI-1 to ob/ob mice led to decreased liver lipid accumulation, further confirming our in vitro experimental results. Finally, we used liver-specific Ogt gene knockout mice fed a high-fat diet to elucidate the specific mechanism of O-GlcNAcylation on NAFLD and found that knockdown of the Ogt gene led to decreased liver lipid accumulation. In conclusion, our findings show that inhibiting the O-GlcNAcylation of FASN at the S1483 site promotes the K48-linked ubiquitination and degradation of FASN and leads to inhibition of lipid accumulation in the liver. Treatment with the OGT inhibitor OSMI-1 leads to decreased lipid accumulation in the liver, suggesting that targeting O-GlcNAcylation sites could be a potential therapeutic strategy for alleviating NAFLD.
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页数:17
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