Xu Allison Wanting, Kaelin Christopher B, Takeda Kiyoshi, Akira Shizuo, Schwartz Michael W, Barsh Gregory S
Department of Genetics, Stanford University School of Medicine, Stanford, California, USA.
J Clin Invest. 2005 Apr;115(4):951-8. doi: 10.1172/JCI24301. Epub 2005 Mar 10.
Central control of energy balance depends on the ability of proopiomelanocortin (POMC) or agouti-related protein (Agrp) hypothalamic neurons to sense and respond to changes in peripheral energy stores. Leptin and insulin have been implicated as circulating indicators of adiposity, but it is not clear how changes in their levels are perceived or integrated by individual neuronal subtypes. We developed mice in which a fluorescent reporter for PI3K activity is targeted to either Agrp or POMC neurons and used 2-photon microscopy to measure dynamic regulation of PI3K by insulin and leptin in brain slices. We show that leptin and insulin act in parallel to stimulate PI3K in POMC neurons but in opposite ways on Agrp neurons. These results suggest a new view of hypothalamic circuitry, in which the effects of leptin and insulin are integrated by anorexigenic but not by orexigenic neurons.
能量平衡的中枢控制取决于促黑素细胞激素原(POMC)或刺鼠相关蛋白(Agrp)下丘脑神经元感知并响应外周能量储备变化的能力。瘦素和胰岛素被认为是肥胖的循环指标,但尚不清楚单个神经元亚型如何感知或整合它们水平的变化。我们构建了小鼠模型,其中PI3K活性的荧光报告基因靶向Agrp或POMC神经元,并使用双光子显微镜测量脑片中胰岛素和瘦素对PI3K的动态调节。我们发现,瘦素和胰岛素协同作用刺激POMC神经元中的PI3K,但对Agrp神经元的作用相反。这些结果提示了下丘脑神经回路的新观点,即瘦素和胰岛素的作用由厌食神经元而非食欲亢进神经元整合。