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转录激活因子 4(ATF4)调节脂质代谢和产热。

ATF4 regulates lipid metabolism and thermogenesis.

机构信息

Key Laboratory of Nutrition and Metabolism, Institute for Nutritional Sciences, Shanghai Institute for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.

出版信息

Cell Res. 2010 Feb;20(2):174-84. doi: 10.1038/cr.2010.4. Epub 2010 Jan 12.

Abstract

Activating transcription factor 4 (ATF4) has been shown to play key roles in many physiological processes. There are no reports, however, demonstrating a direct link between ATF4 and lipid metabolism. We noticed that Atf4-deficient mice are lean, suggesting a possible role for ATF4 in regulating lipid metabolism. The goal of our current study is to investigate the involvement of ATF4 in lipid metabolism and elucidate the underlying mechanisms. Studies using Atf4-deficient mice revealed increased energy expenditure, as measured by oxygen consumption. These mice also showed increases in lipolysis, expression of uncoupling protein 2 (UCP2) and beta-oxidation genes and decreases in expression of lipogenic genes in white adipose tissue (WAT), suggesting increased utilization and decreased synthesis of fatty acids, respectively. Expression of UCP1, 2 and 3 was also increased in brown adipose tissue (BAT), suggesting increased thermogenesis. The effect of ATF4 deletion on expression of UCPs in BAT suggests that increased thermogenesis may underlie increased energy expenditure. Thus, our study identifies a possible new function for ATF4 in regulating lipid metabolism and thermogenesis.

摘要

激活转录因子 4(ATF4)已被证明在许多生理过程中发挥关键作用。然而,目前尚无报告表明 ATF4 与脂质代谢之间存在直接联系。我们注意到,Atf4 缺陷型小鼠体型偏瘦,这表明 ATF4 可能在调节脂质代谢中发挥作用。本研究旨在探讨 ATF4 在脂质代谢中的作用及其潜在机制。使用 Atf4 缺陷型小鼠进行的研究表明,其耗氧量增加,能量消耗增加。这些小鼠的脂肪组织(WAT)中的脂肪分解、解偶联蛋白 2(UCP2)和β-氧化基因的表达增加,而脂肪生成基因的表达减少,这分别表明脂肪酸的利用率增加和合成减少。棕色脂肪组织(BAT)中的 UCP1、2 和 3 的表达也增加,这表明产热增加。ATF4 缺失对 BAT 中 UCPs 表达的影响表明,产热增加可能是能量消耗增加的原因。因此,本研究确定了 ATF4 在调节脂质代谢和产热中的一个新的可能功能。

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