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SIRT4 regulates ATP homeostasis and mediates a retrograde signaling via AMPK

机译:SIRT4调节ATP稳态并通过AMPK介导逆行信号

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摘要

Efficient coupling of cellular energy production to metabolic demand is crucial to maintain organismal homeostasis. Here, we report that the mitochondrial Sirtuin Sirt4 regulates mitochondrial ATP homeostasis. We find that Sirt4 affects mitochondrial uncoupling via the adenine nucleotide translocator 2 (ANT2). Loss of Sirt4 expression leads to decreased cellular ATP levels in vitro and in vivo while Sirt4 overexpression is associated with increased ATP levels. Further, we provide evidence that lack of Sirt4 activates a retrograde signaling response from the mitochondria to the nucleus that includes AMPK, PGC1α, key regulators of β-oxidation such as Acetyl-CoA carboxylase, and components of the mitochondrial respiratory machinery. This study highlights the ability of Sirt4 to regulate ATP levels via ANT2 and a feedback loop involving AMPK.
机译:细胞能量生产与代谢需求的有效结合对于维持机体稳态至关重要。在这里,我们报告线粒体Sirtuin Sirt4调节线粒体ATP稳态。我们发现Sirt4通过腺嘌呤核苷酸转运蛋白2(ANT2)影响线粒体解偶联。 Sirt4表达的丧失导致体外和体内细胞ATP水平降低,而Sirt4过表达与ATP水平升高相关。此外,我们提供的证据表明,缺乏Sirt4会激活从线粒体到细胞核的逆行信号传导反应,包括AMPK,PGC1α,β氧化的关键调节因子(如乙酰辅酶A羧化酶)和线粒体呼吸机的组成部分。这项研究强调了Sirt4通过ANT2和涉及AMPK的反馈回路调节ATP水平的能力。

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