o - glcn酰化通过FASN调控小鼠肝脂合成的机制

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiaoshuang Li, Ziyang Zhang, Meng Zhang, Yu Cao, Wanhui Zhou, Lele Kou, Wenjin Guo, Boxi Zhang, Shize Li, Bin Xu
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引用次数: 0

摘要

非酒精性脂肪性肝病(NAFLD)已成为最常见的慢性肝病之一。β - n -乙酰氨基葡萄糖(O-GlcNAc)的O-Linked attachment of β - n -乙酰氨基葡萄糖(O-GlcNAc)是一种普遍存在的蛋白质翻译后修饰,在体内作为“营养传感器”和“应激受体”,参与维持正常的细胞生理功能。在NAFLD和非酒精性脂肪性肝炎患者的肝脏样本中发现o - glcn酰化水平升高。然而,o - glcn酰化在NAFLD的发展和发病机制中的作用尚不清楚。在这里,我们试图确定o - glcn酰化在NAFLD中的具体作用。本研究结果表明,抑制O-GlcNAc转移酶(OGT)可导致体外肝脂合成基因和蛋白的表达降低。此外,我们发现脂肪酸合成酶(FASN)的表达与o - glcnac酰化水平呈正相关。免疫沉淀和拉下实验证实FASN与OGT在FASN的1483丝氨酸处相互作用,抑制k48相关的FASN泛素化和降解,从而促进肝脏脂质积累和NAFLD的发展。给ob/ob小鼠注射OGT抑制剂OSMI-1,导致肝脏脂质积累减少,进一步证实了我们的体外实验结果。最后,我们用肝脏特异性Ogt基因敲除小鼠喂养高脂肪饮食来阐明o - glcn酰化对NAFLD的特异性机制,发现敲除Ogt基因导致肝脏脂质积累减少。总之,我们的研究结果表明,抑制FASN在S1483位点的o - glcn酰化可促进k48相关的FASN泛素化和降解,从而抑制肝脏中的脂质积累。使用OGT抑制剂OSMI-1治疗可减少肝脏中的脂质积累,这表明靶向o - glcn酰化位点可能是缓解NAFLD的潜在治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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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来源期刊
The FASEB Journal
The FASEB Journal 生物-生化与分子生物学
CiteScore
9.20
自引率
2.10%
发文量
6243
审稿时长
3 months
期刊介绍: The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.
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