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应激门控星形胶质细胞能量储备以损害突触可塑性。

Stress gates an astrocytic energy reservoir to impair synaptic plasticity.

机构信息

Hotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada.

Department of Physiology, David Geffen School of Medicine, University of California Los Angeles, UCLA, Los Angeles, CA, USA.

出版信息

Nat Commun. 2020 Apr 24;11(1):2014. doi: 10.1038/s41467-020-15778-9.

Abstract

Astrocytes support the energy demands of synaptic transmission and plasticity. Enduring changes in synaptic efficacy are highly sensitive to stress, yet whether changes to astrocyte bioenergetic control of synapses contributes to stress-impaired plasticity is unclear. Here we show in mice that stress constrains the shuttling of glucose and lactate through astrocyte networks, creating a barrier for neuronal access to an astrocytic energy reservoir in the hippocampus and neocortex, compromising long-term potentiation. Impairing astrocytic delivery of energy substrates by reducing astrocyte gap junction coupling with dominant negative connexin 43 or by disrupting lactate efflux was sufficient to mimic the effects of stress on long-term potentiation. Furthermore, direct restoration of the astrocyte lactate supply alone rescued stress-impaired synaptic plasticity, which was blocked by inhibiting neural lactate uptake. This gating of synaptic plasticity in stress by astrocytic metabolic networks indicates a broader role of astrocyte bioenergetics in determining how experience-dependent information is controlled.

摘要

星形胶质细胞支持突触传递和可塑性的能量需求。突触效能的持久变化对压力高度敏感,但星形胶质细胞对突触的生物能量控制的变化是否有助于压力损害可塑性尚不清楚。在这里,我们在小鼠中表明,压力限制了葡萄糖和乳酸通过星形胶质细胞网络的穿梭,在海马体和新皮层中为神经元进入星形胶质细胞能量库制造了障碍,从而损害了长时程增强。通过减少星形胶质细胞缝隙连接与显性负性连接蛋白 43 的偶联,或破坏乳酸外排,削弱星形胶质细胞提供能量底物的能力足以模拟压力对长时程增强的影响。此外,仅直接恢复星形胶质细胞的乳酸供应就足以挽救压力引起的突触可塑性障碍,而抑制神经乳酸摄取则阻断了这一过程。星形胶质细胞代谢网络对突触可塑性的这种压力控制表明,星形胶质细胞生物能量在决定经验依赖性信息如何被控制方面发挥着更广泛的作用。

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