Supramolecular aggregation of aquaporin-4 shapes astrocyte collective migration and mechanics

Aquaporin-4 (AQP4), the main astrocytic water channel, assembles into supramolecular structures known as Orthogonal Arrays of Particles (OAPs). While AQP4-mediated water fluxes are known to influence cytoskeletal dynamics at the single-cell level, their role in collective migration remain unclear. Using primary WT and OAP-deficient (OAP-null) astrocytes, we investigated cell migration under control and proinflammatory conditions. In wound healing assays, control OAP-null astrocytes exhibited greater migratory capacity, while inflamed cells were largely immotile. Particle Image Velocimetry revealed genotype and condition-specific migration patterns, with OAP-null astrocytes displaying more linear trajectories. Cytokine treatment also reduced AQP4 and Connexin-43 expression and impaired gap-junctional communication in both genotypes. Calcein-AM quenching assays showed reduced water permeability in OAP-null cells, independently of treatment. These findings highlight the supramolecular organization of AQP4 as a key determinant of astrocyte collective migration and suggest that chronic inflammation induces a poorly coordinated phenotype through dysregulation of AQP4 and gap-junctional networks.

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Publication Details

Journal
Scientific Reports
Published
2026-01-22
DOI
https://doi.org/10.1038/s41598-026-35900-z
Citations
1
Primary Topic
Ion Transport and Channel Regulation
Type
article
Field-Weighted Citation Impact
22.24
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article

Supramolecular aggregation of aquaporin-4 shapes astrocyte collective migration and mechanics

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article

Supramolecular aggregation of aquaporin-4 shapes astrocyte collective migration and mechanics

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article en
1 citations

Abstract

Aquaporin-4 (AQP4), the main astrocytic water channel, assembles into supramolecular structures known as Orthogonal Arrays of Particles (OAPs). While AQP4-mediated water fluxes are known to influence cytoskeletal dynamics at the single-cell level, their role in collective migration remain unclear. Using primary WT and OAP-deficient (OAP-null) astrocytes, we investigated cell migration under control and proinflammatory conditions. In wound healing assays, control OAP-null astrocytes exhibited greater migratory capacity, while inflamed cells were largely immotile. Particle Image Velocimetry revealed genotype and condition-specific migration patterns, with OAP-null astrocytes displaying more linear trajectories. Cytokine treatment also reduced AQP4 and Connexin-43 expression and impaired gap-junctional communication in both genotypes. Calcein-AM quenching assays showed reduced water permeability in OAP-null cells, independently of treatment. These findings highlight the supramolecular organization of AQP4 as a key determinant of astrocyte collective migration and suggest that chronic inflammation induces a poorly coordinated phenotype through dysregulation of AQP4 and gap-junctional networks.

Scientific ReportsVol. 16(1)
Institute of Organic Synthesis and Photoreactivity (IT), LUM Jean Monnet University (IT), National Research Council (IT), University of Bari Aldo Moro (IT), University of Maryland, College Park (US)
Openalex Percentile: Top 2%
Ion Transport and Channel Regulation
22.24
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