A GPRC5B–Fyn signaling axis regulates VRAC activity by targeting LRRC8A

The mechanisms by which physiological signals gate the volume-regulated anion channel (VRAC) remain poorly understood. Here, we identify a GPRC5B-Fyn signaling axis that directly controls VRAC activation by targeting the essential subunit LRRC8A. We found that the orphan G protein-coupled receptor GPRC5B binds LRRC8A and recruits the Src family kinase Fyn, which in turn suppresses hypotonicity-evoked VRAC activation. Disrupting Fyn binding to GPRC5B or substituting a predicted phosphorylation site on LRRC8A (Y362) abolishes this inhibition. Across primary astrocytes and reconstituted systems, GPRC5B prevents the intersubunit conformational rearrangements associated with VRAC opening without altering basal channel expression. In astrocytes, the MLC protein MLC1 partially sequesters GPRC5B, thereby reducing the GPRC5B-LRRC8A interaction, providing a mechanistic link to VRAC dysfunction in megalencephalic leukoencephalopathy. These results reveal a receptor-kinase-channel pathway that gates VRAC through Y362-dependent modulation of LRRC8A, establishing a molecular framework for VRAC regulation and its disruption in disease.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-10-15
DOI
https://doi.org/10.1073/pnas.2606899123
Primary Topic
Ion Transport and Channel Regulation
Type
article
Field-Weighted Citation Impact
0.00
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article

A GPRC5B–Fyn signaling axis regulates VRAC activity by targeting LRRC8A

Yulia Kostritskaia, Héctor Gaitán‐Peñas, Raúl Estévez, Ekaitz Errasti‐Murugarren et al.
Proceedings of the National Academy of Sciences
Ion Transport and Channel Regulation
article

A GPRC5B–Fyn signaling axis regulates VRAC activity by targeting LRRC8A

Yulia Kostritskaia, Héctor Gaitán‐Peñas, Raúl Estévez, Ekaitz Errasti‐Murugarren, Michael Pusch, Marta Alonso-Gardón, Tobias Stauber, Malte Klüssendorf, Tania López-Hernández, Aida Castellanos, Adrià Pla-Casillanis, Marc González‐Subías, Sara Bertelli, Guillem Pont-Espinós
article en

Abstract

The mechanisms by which physiological signals gate the volume-regulated anion channel (VRAC) remain poorly understood. Here, we identify a GPRC5B-Fyn signaling axis that directly controls VRAC activation by targeting the essential subunit LRRC8A. We found that the orphan G protein-coupled receptor GPRC5B binds LRRC8A and recruits the Src family kinase Fyn, which in turn suppresses hypotonicity-evoked VRAC activation. Disrupting Fyn binding to GPRC5B or substituting a predicted phosphorylation site on LRRC8A (Y362) abolishes this inhibition. Across primary astrocytes and reconstituted systems, GPRC5B prevents the intersubunit conformational rearrangements associated with VRAC opening without altering basal channel expression. In astrocytes, the MLC protein MLC1 partially sequesters GPRC5B, thereby reducing the GPRC5B-LRRC8A interaction, providing a mechanistic link to VRAC dysfunction in megalencephalic leukoencephalopathy. These results reveal a receptor-kinase-channel pathway that gates VRAC through Y362-dependent modulation of LRRC8A, establishing a molecular framework for VRAC regulation and its disruption in disease.

Proceedings of the National Academy of SciencesVol. 123(42)
Universitat Autònoma de Barcelona (ES), Instituto de Salud Carlos III (ES), Humboldt-Universität zu Berlin (DE), Institut d'Investigació Biomédica de Bellvitge (ES), MSH Medical School Hamburg – University of Applied Sciences and Medical University (DE), Centre for Biomedical Network Research on Rare Diseases (ES), Department of Physiological Sciences (RU), Instituto di Biofisica (ES), National Research Council (IT)
Good health and well-being
Openalex Percentile: Top 24%
Ion Transport and Channel Regulation
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