Orozco-Solis Ricardo, Aguilar-Arnal Lorena, Murakami Mari, Peruquetti Rita, Ramadori Giorgio, Coppari Roberto, Sassone-Corsi Paolo
Center for Epigenetics and Metabolism, Unite 904 INSERM, Department of Biological Chemistry, University of California, Irvine, Irvine, CA 92697, USA.
CMU Departement Phyme, Universite de Geneve, rue Michel Servet 1, 1211 Geneva, Switzerland.
Cell Metab. 2016 Mar 8;23(3):467-78. doi: 10.1016/j.cmet.2016.02.003.
Organismal homeostasis relies on coherent interactions among tissues, specifically between brain-driven functions and peripheral metabolic organs. Hypothalamic circuits compute metabolic information to optimize energetic resources, but the role of the circadian clock in these pathways remains unclear. We have generated mice with targeted ablation of the core-clock gene Bmal1 within Sf1-neurons of the ventromedial hypothalamus (VMH). While this mutation does not affect the central clock in the suprachiasmatic nucleus (SCN), the VMH clock controls cyclic thermogenesis in brown adipose tissue (BAT), a tissue that governs energy balance by dissipating chemical energy as heat. VMH-driven control is exerted through increased adrenergic signaling within the sympathetic nervous system, without affecting the BAT's endogenous clock. Moreover, we show that the VMH circadian clock computes light and feeding inputs to modulate basal energy expenditure. Thus, we reveal a previously unsuspected circuit where an SCN-independent, hypothalamic circadian clock controls BAT function, energy expenditure, and thermogenesis.
机体的稳态依赖于组织之间的协调相互作用,特别是脑驱动功能与外周代谢器官之间的相互作用。下丘脑回路计算代谢信息以优化能量资源,但生物钟在这些途径中的作用仍不清楚。我们已经构建了在腹内侧下丘脑(VMH)的Sf1神经元中靶向敲除核心生物钟基因Bmal1的小鼠。虽然这种突变不影响视交叉上核(SCN)中的中央生物钟,但VMH生物钟控制棕色脂肪组织(BAT)中的周期性产热,BAT是一种通过将化学能以热量形式散发来控制能量平衡的组织。VMH驱动的控制是通过交感神经系统内肾上腺素能信号的增加来实现的,而不影响BAT的内源性生物钟。此外,我们表明VMH生物钟计算光和进食输入以调节基础能量消耗。因此,我们揭示了一个以前未被怀疑的回路,其中一个独立于SCN的下丘脑生物钟控制BAT功能、能量消耗和产热。