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营养感应 AgRP 神经元在能量匮乏期间传递对肝脏自噬的控制作用。

Nutrient-sensing AgRP neurons relay control of liver autophagy during energy deprivation.

机构信息

Max Planck Institute for Metabolism Research, Department of Neuronal Control of Metabolism, Gleueler Str. 50, 50931 Cologne, Germany; Policlinic for Endocrinology, Diabetes, and Preventive Medicine (PEDP), University Hospital Cologne, Kerpener Str. 26, 50924 Cologne, Germany; Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (CECAD) and Center of Molecular Medicine Cologne (CMMC), University of Cologne, Joseph-Stelzmann-Str. 26, 50931 Cologne, Germany.

Max Planck Institute for Biology of Ageing, Joseph-Stelzmann-Strasse 9B, 50931 Cologne, Germany.

出版信息

Cell Metab. 2023 May 2;35(5):786-806.e13. doi: 10.1016/j.cmet.2023.03.019. Epub 2023 Apr 18.

Abstract

Autophagy represents a key regulator of aging and metabolism in sensing energy deprivation. We find that fasting in mice activates autophagy in the liver paralleled by activation of hypothalamic AgRP neurons. Optogenetic and chemogenetic activation of AgRP neurons induces autophagy, alters phosphorylation of autophagy regulators, and promotes ketogenesis. AgRP neuron-dependent induction of liver autophagy relies on NPY release in the paraventricular nucleus of the hypothalamus (PVH) via presynaptic inhibition of NPY1R-expressing neurons to activate PVH neurons. Conversely, inhibiting AgRP neurons during energy deprivation abrogates induction of hepatic autophagy and rewiring of metabolism. AgRP neuron activation increases circulating corticosterone concentrations, and reduction of hepatic glucocorticoid receptor expression attenuates AgRP neuron-dependent activation of hepatic autophagy. Collectively, our study reveals a fundamental regulatory principle of liver autophagy in control of metabolic adaptation during nutrient deprivation.

摘要

自噬代表了在感知能量匮乏时调节衰老和代谢的关键因素。我们发现,在小鼠中禁食会激活肝脏中的自噬,同时激活下丘脑 AgRP 神经元。光遗传学和化学遗传学激活 AgRP 神经元会诱导自噬,改变自噬调节剂的磷酸化,并促进酮体生成。AgRP 神经元依赖性诱导肝脏自噬依赖于在下丘脑室旁核(PVH)中通过抑制表达 NPY1R 的神经元的突触前抑制释放 NPY 来激活 PVH 神经元。相反,在能量剥夺期间抑制 AgRP 神经元会消除肝自噬的诱导和代谢的重编程。AgRP 神经元的激活会增加循环皮质酮浓度,减少肝糖皮质激素受体表达会减弱 AgRP 神经元依赖性的肝自噬激活。总的来说,我们的研究揭示了在营养缺乏期间控制代谢适应的肝脏自噬的基本调节原则。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974d/10173804/4a09aaa113ce/fx1.jpg

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