Meningeal lymphatics-microglia axis regulates synaptic physiology

Meningeal lymphatics serve as an outlet for cerebrospinal fluid, and their dysfunction is associated with various neurodegenerative conditions. Previous studies have demonstrated that dysfunctional meningeal lymphatics evoke behavioral changes, but the neural mechanisms underlying these changes have remained elusive. Here, we show that prolonged impairment of meningeal lymphatics alters the balance of cortical excitatory and inhibitory synaptic inputs, accompanied by deficits in memory tasks. These synaptic and behavioral alterations induced by lymphatic dysfunction are mediated by microglia, leading to increased expression of the interleukin 6 gene (Il6). IL-6 drives inhibitory synapse phenotypes via a combination of trans- and classical IL-6 signaling. Restoring meningeal lymphatic function in aged mice reverses age-associated synaptic and behavioral alterations. Our findings suggest that dysfunctional meningeal lymphatics adversely impact cortical circuitry through an IL-6-dependent mechanism and identify a potential target for treating aging-associated cognitive decline.

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Publication Details

Journal
Cell
Published
2025-03-22
DOI
https://doi.org/10.1016/j.cell.2025.02.022
Citations
46
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
38.74
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article

Meningeal lymphatics-microglia axis regulates synaptic physiology

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46 citations
Cell
Neuroinflammation and Neurodegeneration Mechanisms
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article

Meningeal lymphatics-microglia axis regulates synaptic physiology

Kyungdeok Kim, Zachary Papadopoulos, Siling Du, Jean‐Léon Thomas, Jay Cao, Marco Colonna, Jasmin Herz, Jonathan Kipnis, Igor Smirnov, Daviti Abramishvili
article en
46 citations

Abstract

Meningeal lymphatics serve as an outlet for cerebrospinal fluid, and their dysfunction is associated with various neurodegenerative conditions. Previous studies have demonstrated that dysfunctional meningeal lymphatics evoke behavioral changes, but the neural mechanisms underlying these changes have remained elusive. Here, we show that prolonged impairment of meningeal lymphatics alters the balance of cortical excitatory and inhibitory synaptic inputs, accompanied by deficits in memory tasks. These synaptic and behavioral alterations induced by lymphatic dysfunction are mediated by microglia, leading to increased expression of the interleukin 6 gene (Il6). IL-6 drives inhibitory synapse phenotypes via a combination of trans- and classical IL-6 signaling. Restoring meningeal lymphatic function in aged mice reverses age-associated synaptic and behavioral alterations. Our findings suggest that dysfunctional meningeal lymphatics adversely impact cortical circuitry through an IL-6-dependent mechanism and identify a potential target for treating aging-associated cognitive decline.

CellVol. 188(10)
Washington University in St. Louis (US), Sorbonne Université (FR)
Zero hunger
Openalex Percentile: Top 0%
Neuroinflammation and Neurodegeneration Mechanisms
38.74
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