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

IF 14.7 1区 医学 Q1 NEUROSCIENCES
Neuron Pub Date : 2024-09-25 Epub Date: 2024-07-25 DOI:10.1016/j.neuron.2024.06.029
Hannah Scheiblich, Frederik Eikens, Lena Wischhof, Sabine Opitz, Kay Jüngling, Csaba Cserép, Susanne V Schmidt, Jessica Lambertz, Tracy Bellande, Balázs Pósfai, Charlotte Geck, Jasper Spitzer, Alexandru Odainic, Sergio Castro-Gomez, Stephanie Schwartz, Ibrahim Boussaad, Rejko Krüger, Enrico Glaab, Donato A Di Monte, Daniele Bano, Ádám Dénes, Eike Latz, Ronald Melki, Hans-Christian Pape, Michael T Heneka
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引用次数: 0

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.

小胶质细胞通过隧道纳米管拯救神经元,使其免于聚集体诱发的神经元功能障碍和死亡。
小胶质细胞对维持大脑健康和神经元功能至关重要。在这里,我们报告了小胶质细胞在生理和病理条件下利用隧道纳米管(TNTs)与神经元建立连接的情况。这些 TNTs 可促进细胞器、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的毒性聚集体会在神经元内积聚。我们的研究表明,小胶质细胞利用 TNTs 将神经元从这些聚集体中提取出来,从而恢复神经元的健康。此外,小胶质细胞还能与有负担的神经元分享它们健康的线粒体,从而减少氧化应激并使基因表达正常化。在TNT形成前用抗霉素A破坏线粒体功能,就会消除这种神经保护作用。此外,将神经元与小胶质细胞共同培养并促进 TNT 的形成,还能挽救因 α-syn 或 tau 聚集而受到抑制的神经元活动。值得注意的是,在携带 Lrrk22(Gly2019Ser)或 Trem2(T66M)和(R47H)突变的小胶质细胞中,TNT 介导的聚集体转移会受到影响,这表明这些基因变体在神经退行性疾病的病理学中发挥作用。
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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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