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海马体α-突触核蛋白介导抑郁样行为。

Hippocampal alpha-synuclein mediates depressive-like behaviors.

机构信息

Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming 650118, China; Neuroscience Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100005, China.

Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming 650118, China.

出版信息

Brain Behav Immun. 2021 Jul;95:226-237. doi: 10.1016/j.bbi.2021.03.020. Epub 2021 Mar 26.

Abstract

Alpha-synuclein (α-syn) which encoded by SNCA plays a critical role in the neurotransmission, vesicle dynamics, and neuroplasticity. Alteration to SNCA expression is associated with major depressive disorder. However, the pathogenic mechanism of SNCA in depression remains unknown. Herein, we reported that SNCA was up-regulated in the peripheral blood of major depressive disorder (MDD) patients and the depressive mice. Chronic restraint stress (CRS) also up-regulated the SNCA expression in the hippocampus. Moreover, over-expression of SNCA in the hippocampus triggered spontaneous depressive-like behaviors under the non-stressed conditions in mice, and knockout of SNCA could reverse CRS-induced depressive-like behaviors. SNCA led to synapse loss and neuronal cell death in the hippocampus possibly via complement-mediated microglial engulfment and inflammation, and thus contributed to the pathogenesis of depressive disorder. Overall, hippocampal SNCA and complement system are involved in the pathogenesis of depressive disorder and it provides a new perspective for the occurrence of depressive disorder.

摘要

α-突触核蛋白(α-syn)由 SNCA 编码,在神经传递、囊泡动力学和神经可塑性中发挥关键作用。SNCA 表达的改变与重度抑郁症有关。然而,SNCA 在抑郁症中的致病机制尚不清楚。在此,我们报道了 SNCA 在重度抑郁症(MDD)患者和抑郁小鼠的外周血中上调。慢性束缚应激(CRS)也会在上调海马中的 SNCA 表达。此外,在小鼠非应激条件下,过表达 SNCA 会引发自发性抑郁样行为,而 SNCA 的敲除则可以逆转 CRS 引起的抑郁样行为。SNCA 可能通过补体介导的小胶质细胞吞噬和炎症导致海马中的突触损失和神经元细胞死亡,从而导致抑郁障碍的发病。总的来说,海马中的 SNCA 和补体系统参与了抑郁障碍的发病机制,为抑郁障碍的发生提供了新的视角。

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