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脑和肌肉芳香烃受体核转运蛋白样蛋白1与过氧化物酶体增殖物激活受体α的相互调节在啮齿动物肝脏生物钟中定义了一个新的正反馈回路。

Reciprocal regulation of brain and muscle Arnt-like protein 1 and peroxisome proliferator-activated receptor alpha defines a novel positive feedback loop in the rodent liver circadian clock.

作者信息

Canaple Laurence, Rambaud Juliette, Dkhissi-Benyahya Ouria, Rayet Béatrice, Tan Nguan Soon, Michalik Liliane, Delaunay Franck, Wahli Walter, Laudet Vincent

机构信息

Structure and Evolution of Nuclear Receptors, Centre National de la Recherche Scientifique (CNRS) Unité Mixte de Recherche 5161, Institut Fédératif de Recherche (IFR) 128 BioSciences Lyon-Gerland, Lyon, France.

出版信息

Mol Endocrinol. 2006 Aug;20(8):1715-27. doi: 10.1210/me.2006-0052. Epub 2006 Mar 23.

DOI:10.1210/me.2006-0052
PMID:16556735
Abstract

Recent evidence has emerged that peroxisome proliferator-activated receptor alpha (PPARalpha), which is largely involved in lipid metabolism, can play an important role in connecting circadian biology and metabolism. In the present study, we investigated the mechanisms by which PPARalpha influences the pacemakers acting in the central clock located in the suprachiasmatic nucleus and in the peripheral oscillator of the liver. We demonstrate that PPARalpha plays a specific role in the peripheral circadian control because it is required to maintain the circadian rhythm of the master clock gene brain and muscle Arnt-like protein 1 (bmal1) in vivo. This regulation occurs via a direct binding of PPARalpha on a potential PPARalpha response element located in the bmal1 promoter. Reversely, BMAL1 is an upstream regulator of PPARalpha gene expression. We further demonstrate that fenofibrate induces circadian rhythm of clock gene expression in cell culture and up-regulates hepatic bmal1 in vivo. Together, these results provide evidence for an additional regulatory feedback loop involving BMAL1 and PPARalpha in peripheral clocks.

摘要

最近有证据表明,在很大程度上参与脂质代谢的过氧化物酶体增殖物激活受体α(PPARα),在连接昼夜节律生物学和代谢方面可发挥重要作用。在本研究中,我们探究了PPARα影响位于视交叉上核的中央时钟和肝脏外周振荡器中的起搏器的机制。我们证明PPARα在外周昼夜节律控制中发挥特定作用,因为在体内维持主时钟基因脑和肌肉芳香烃受体核转运蛋白样蛋白1(bmal1)的昼夜节律需要PPARα。这种调节通过PPARα直接结合位于bmal1启动子上的潜在PPARα反应元件来实现。相反,BMAL1是PPARα基因表达的上游调节因子。我们进一步证明非诺贝特在细胞培养中诱导时钟基因表达的昼夜节律,并在体内上调肝脏bmal1。总之,这些结果为在外周时钟中涉及BMAL1和PPARα的额外调节反馈环提供了证据。

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