Microglia-glioblastoma crosstalk mediates glioblastoma invasion at the far infiltration zone

Glioblastoma (GB) cells infiltrate the brain parenchyma and colonize distant regions, driving recurrence and therapy resistance. Here, we examined dynamic microglial responses to infiltrating tumor cells during GB progression. Three-photon imaging in an autochthonous, immunocompetent GB mouse model enabled visualization of microglia-GB interactions at the far infiltration zone (FIZ) in the corpus callosum (CC). GB infiltration speed varied by anatomical location and tumor microtube (TM) number. Microglia increased surveillance in sparsely infiltrated areas but reduced it with higher GB density, revealing a biphasic response. Directional migration toward GB cells was restricted to microglial subsets within a defined spatial range, indicating heterogeneous reactivity. CX3CR1 deficiency enhanced microglial reactivity while limiting GB cell migration. Microglia depletion with the CSF1R inhibitor PLX5622 reduced GB cell migration and constrained TM plasticity. Thus, microglia respond to GB cell infiltration in a stage-dependent manner and critically modulate dissemination at the FIZ.

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Publication Details

Journal
Immunity
Published
2026-03-31
DOI
https://doi.org/10.1016/j.immuni.2026.03.010
Primary Topic
Glioma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Microglia-glioblastoma crosstalk mediates glioblastoma invasion at the far infiltration zone

Simona Parrinello, Henrike Antony, U. Herrlinger, Manuel Mittag et al.
Immunity
Glioma Diagnosis and Treatment
article

Microglia-glioblastoma crosstalk mediates glioblastoma invasion at the far infiltration zone

Simona Parrinello, Henrike Antony, U. Herrlinger, Manuel Mittag, M. Hölzel, Qihui Zhou, Daniele Bano, Severin Filser, Miriam Stork, Paolo Salomoni, Falko Fuhrmann, Sonia Leonardelli, Fabrizio Musacchio, Martin Fuhrmann, Felix Christopher Nebeling, Torsten Pietsch, Deli A., Frank A. Giordano, Lea L. Friker, Nala Gockel
article en

Abstract

Glioblastoma (GB) cells infiltrate the brain parenchyma and colonize distant regions, driving recurrence and therapy resistance. Here, we examined dynamic microglial responses to infiltrating tumor cells during GB progression. Three-photon imaging in an autochthonous, immunocompetent GB mouse model enabled visualization of microglia-GB interactions at the far infiltration zone (FIZ) in the corpus callosum (CC). GB infiltration speed varied by anatomical location and tumor microtube (TM) number. Microglia increased surveillance in sparsely infiltrated areas but reduced it with higher GB density, revealing a biphasic response. Directional migration toward GB cells was restricted to microglial subsets within a defined spatial range, indicating heterogeneous reactivity. CX3CR1 deficiency enhanced microglial reactivity while limiting GB cell migration. Microglia depletion with the CSF1R inhibitor PLX5622 reduced GB cell migration and constrained TM plasticity. Thus, microglia respond to GB cell infiltration in a stage-dependent manner and critically modulate dissemination at the FIZ.

ImmunityVol. 59(4)
University of Bonn (DE), Heidelberg University (DE), University Hospital Bonn (DE), German Center for Neurodegenerative Diseases (DE), University Hospital Heidelberg (DE), London Cancer (GB), University Medical Centre Mannheim (DE), University College London (GB)
Land Nordrhein-Westfalen, Deutsches Krebsforschungszentrum, Wilhelm Sander-Stiftung, Deutsche Forschungsgemeinschaft, Deutsches Zentrum für Neurodegenerative Erkrankungen, Deutsche Krebshilfe, Ministerium für Kultur und Wissenschaft des Landes Nordrhein-Westfalen, World Cancer Research Fund, European Research Council
Openalex Percentile: Top 31%
Glioma Diagnosis and Treatment
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