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小胶质细胞通过形成隧道纳米管来挽救聚集诱导的神经元功能障碍和死亡。

Microglia rescue neurons from aggregate-induced neuronal dysfunction and death through tunneling nanotubes.

机构信息

Institute of Clinical Chemistry and Clinical Pharmacology, University Hospital Bonn, Bonn, Germany; German Center for Neurodegenerative Diseases, Bonn, Germany; Max-Planck-Institute for Biology of Ageing, Cologne, Germany.

German Center for Neurodegenerative Diseases, Bonn, Germany; Max-Planck-Institute for Biology of Ageing, Cologne, Germany.

出版信息

Neuron. 2024 Sep 25;112(18):3106-3125.e8. doi: 10.1016/j.neuron.2024.06.029. Epub 2024 Jul 25.

Abstract

Microglia are crucial for maintaining brain health and neuron function. Here, we report that microglia establish connections with neurons using tunneling nanotubes (TNTs) in both physiological and pathological conditions. These TNTs facilitate the rapid exchange of organelles, vesicles, and proteins. In neurodegenerative diseases like Parkinson's and Alzheimer's disease, toxic aggregates of alpha-synuclein (α-syn) and tau accumulate within neurons. Our research demonstrates that microglia use TNTs to extract neurons from these aggregates, restoring neuronal health. Additionally, microglia share their healthy mitochondria with burdened neurons, reducing oxidative stress and normalizing gene expression. Disrupting mitochondrial function with antimycin A before TNT formation eliminates this neuroprotection. Moreover, co-culturing neurons with microglia and promoting TNT formation rescues suppressed neuronal activity caused by α-syn or tau aggregates. Notably, TNT-mediated aggregate transfer is compromised in microglia carrying Lrrk22(Gly2019Ser) or Trem2(T66M) and (R47H) mutations, suggesting a role in the pathology of these gene variants in neurodegenerative diseases.

摘要

小胶质细胞对于维持大脑健康和神经元功能至关重要。在这里,我们报告称,在生理和病理条件下,小胶质细胞通过隧道纳米管(TNTs)与神经元建立连接。这些 TNTs 促进了细胞器、囊泡和蛋白质的快速交换。在帕金森病和阿尔茨海默病等神经退行性疾病中,α-突触核蛋白(α-syn)和 tau 的有毒聚集体在神经元内积累。我们的研究表明,小胶质细胞利用 TNTs 从这些聚集体中提取神经元,从而恢复神经元的健康。此外,小胶质细胞将其健康的线粒体与负担过重的神经元共享,从而减轻氧化应激并使基因表达正常化。在用 antimycin A 破坏 TNT 形成之前,线粒体功能的破坏消除了这种神经保护作用。此外,与小胶质细胞共培养并促进 TNT 形成可挽救由α-syn 或 tau 聚集体引起的抑制性神经元活性。值得注意的是,携带 Lrrk22(Gly2019Ser)或 Trem2(T66M)和 (R47H)突变的小胶质细胞中的 TNT 介导的聚集体转移受损,这表明它们在这些基因突变导致的神经退行性疾病的发病机制中发挥作用。

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