DFCP1 是饥饿驱动的 ATGL 介导的脂滴溶脂的调节器

IF 5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
V A Ismail, M N Harvey, Zak Baker, J Castillo-Badillo, T Naismith, D J Pagliarini, D J Kast
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引用次数: 0

摘要

脂滴(LDs)是一种瞬时脂质储存细胞器,可随时为细胞补充能量或脂质基块,因此在细胞代谢中发挥着核心作用。双FYVE结构域含蛋白1(DFCP1/ZFYV1)已成为LD新陈代谢的关键调控因子,DFCP1在LD上的核苷酸依赖性积累影响着LD的大小、数量和动态。在这里,我们发现 DFCP1 通过直接调节脂肪甘油三酯脂酶(ATGL/PNPLA2)的活性来调控脂质代谢,ATGL/PNPLA2 是驱动 LDs 分解代谢的限速脂酶。我们通过对与低密度脂蛋白代谢相关的关键酶进行药理抑制,发现 DFCP1 专门调节脂肪分解,并在较小程度上调节脂肪吞噬。与这一观察结果一致的是,在饥饿细胞中,DFCP1 与 ATGL 相互作用并将 ATGL 募集到低密度脂蛋白上,而与 ATGL 的其他已知调控因子无关。我们进一步证实,这种相互作用阻止了 ATGL 与 LD 的动态分离,从而阻碍了 LD 的脂肪分解率。总之,我们的研究结果表明,DFCP1 是一种对营养敏感的 LD 分解调节因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DFCP1 is a Regulator of Starvation-driven ATGL-mediated Lipid Droplet Lipolysis.

Lipid droplets (LDs) are transient lipid storage organelles that can be readily tapped to resupply cells with energy or lipid building blocks, and therefore play a central role in cellular metabolism. Double FYVE Domain Containing Protein 1 (DFCP1/ZFYV1) has emerged as a key regulator of LD metabolism, where the nucleotide-dependent accumulation of DFCP1 on LDs influences their size, number, and dynamics. Here we show that DFCP1 regulates lipid metabolism by directly modulating the activity of Adipose Triglyceride Lipase (ATGL/PNPLA2), the rate-limiting lipase driving the catabolism of LDs. We show through pharmacological inhibition of key enzymes associated with LD metabolism that DFCP1 specifically regulates lipolysis and, to a lesser extent, lipophagy. Consistent with this observation, DFCP1 interacts with and recruits ATGL to LDs in starved cells, irrespective of other known regulatory factors of ATGL. We further establish that this interaction prevents dynamic disassociation of ATGL from LDs and thereby impedes the rate of LD lipolysis. Collectively, our findings indicate that DFCP1 is a nutrient-sensitive regulator of LD catabolism.

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来源期刊
Journal of Lipid Research
Journal of Lipid Research 生物-生化与分子生物学
CiteScore
11.10
自引率
4.60%
发文量
146
审稿时长
41 days
期刊介绍: The Journal of Lipid Research (JLR) publishes original articles and reviews in the broadly defined area of biological lipids. We encourage the submission of manuscripts relating to lipids, including those addressing problems in biochemistry, molecular biology, structural biology, cell biology, genetics, molecular medicine, clinical medicine and metabolism. Major criteria for acceptance of articles are new insights into mechanisms of lipid function and metabolism and/or genes regulating lipid metabolism along with sound primary experimental data. Interpretation of the data is the authors’ responsibility, and speculation should be labeled as such. Manuscripts that provide new ways of purifying, identifying and quantifying lipids are invited for the Methods section of the Journal. JLR encourages contributions from investigators in all countries, but articles must be submitted in clear and concise English.
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