ChREBP介导fbp1缺陷肝脏代谢重塑

IF 5 2区 生物学 Q2 CELL BIOLOGY
Chen-Ma Wang, Qiu-Fang Bai, Ya-Jin Liu, Jie Lin, Chun-Chun Wei, Xian-Hua Ma, Jia-Mu Zhao, Meng Zhu, Yu-Xia Chen, Ya-Nan Shi, Jian-Hui Shi, Weiping J Zhang
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引用次数: 0

摘要

果糖-1,6-二磷酸酶 1(FBP1)是葡萄糖生成过程中的一个关键酶,它的缺乏会导致脂肪肝。然而,其潜在机制和生理意义尚未完全明了。在这里,我们证明了碳水化合物反应元件结合蛋白(ChREBP)介导脂质代谢重塑,并促进甘油三酯在成人 FBP1 缺陷肝脏中进行性积累以对抗代谢损伤。诱导性肝脏特异性缺失 Fbp1 基因会导致进行性肝肿大和肝脂肪变性,肝脏新生脂肪生成(DNL)显著增加,血浆β-羟丁酸水平下降。值得注意的是,即使在禁食条件下,FBP1 缺乏也会导致 ChREBP 及其参与糖酵解、脂肪生成和脂肪酸氧化的靶基因持续活化。此外,肝脏特异性 ChREBP 干扰可明显恢复 FBP1 缺乏肝脏中 DNL 和甘油三酯积累增强的表型,但会加剧其肝肿大和肝损伤,这与显著的能量不足、mTOR 激活受损和氧化应激增加有关。此外,代谢组学分析表明,在 FBP1 缺失的肝脏中,ChREBP 缺失导致磷酸烯醇丙酮酸、磷酸甘油酸、磷脂和神经酰胺显著升高。综上所述,这些结果表明,在缺乏 FBP1 的情况下,ChREBP 通路的过度激活介导了肝脏代谢重塑,这有助于渐进性肝脂肪变性的发病机制,并提供了对肝损伤的保护。因此,我们的研究结果表明,ChREBP 在葡萄糖生成中间体过多的情况下对代谢重塑起着有益的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ChREBP mediates metabolic remodeling in FBP1-deficient liver.

The deficiency of fructose-1,6-bisphosphatase 1 (FBP1), a key enzyme of gluconeogenesis, causes fatty liver. However, its underlying mechanism and physiological significance are not fully understood. Here we demonstrate that carbohydrate response element-binding protein (ChREBP) mediates lipid metabolic remodeling and promotes progressive triglyceride accumulation against metabolic injury in adult FBP1-deficient liver. Inducible liver-specific deletion of Fbp1 gene caused progressive hepatomegaly and hepatic steatosis, with a marked increase in hepatic de novo lipogenesis (DNL) as well as a decrease in plasma β-hydroxybutyrate levels. Notably, FBP1 deficiency resulted in a persistent activation of ChREBP and its target genes involved in glycolysis, lipogenesis, and fatty acid oxidation, even under fasting conditions. Furthermore, liver-specific ChREBP disruption could markedly restore the phenotypes of enhanced DNL and triglyceride accumulation in FBP1-deficient liver but exacerbated its hepatomegaly and liver injury, which was associated with remarkable energy deficit, impaired mammalian target of rapamycin (mTOR) activation, and increased oxidative stress. Furthermore, metabolomics analysis revealed a robust elevation of phosphoenolpyruvate, phosphoglycerates, phospholipids, and ceramides caused by ChREBP deletion in FBP1-deficient liver. Put together, these results suggest that overactivation of ChREBP pathway mediates liver metabolic remodeling in the absence of FBP1, which contributes to the pathogenesis of progressive hepatic steatosis and provides a protection against liver injury. Thus, our findings point to a beneficial role of ChREBP in metabolic remodeling in the context of excessive gluconeogenic intermediates.NEW & NOTEWORTHY FBP1 deficiency in adulthood causes progressive hepatic steatosis due to the overactivation of ChREBP pathway, which enhances lipid synthesis and inhibits fat oxidation. ChREBP-mediated metabolic remodeling protects against liver injury caused by energy deficit and oxidative stress in FBP1-deficient liver.

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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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