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

Authors :
Scheiblich H
Eikens F
Wischhof L
Opitz S
Jüngling K
Cserép C
Schmidt SV
Lambertz J
Bellande T
Pósfai B
Geck C
Spitzer J
Odainic A
Castro-Gomez S
Schwartz S
Boussaad I
Krüger R
Glaab E
Di Monte DA
Bano D
Dénes Á
Latz E
Melki R
Pape HC
Heneka MT
Source :
Neuron [Neuron] 2024 Sep 25; Vol. 112 (18), pp. 3106-3125.e8. Date of Electronic Publication: 2024 Jul 25.
Publication Year :
2024

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.<br />Competing Interests: Declaration of interests E.L. is a co-founder and advisor at IFM Therapeutics, and M.T.H. serves as an advisory board member at IFM Therapeutics, T3D, and Alector.<br /> (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-4199
Volume :
112
Issue :
18
Database :
MEDLINE
Journal :
Neuron
Publication Type :
Academic Journal
Accession number :
39059388
Full Text :
https://doi.org/10.1016/j.neuron.2024.06.029