bioRxivCell BiologyPreprint
Endothelial gain of PIEZO/TRPV mechanosensors drives cavernous malformations
J de Jong, Candice PasquieriD, T. Manicom Ramsamy, A. Ahmed, A. Onisiforou, C. Roedel, Fabrice SengeriD, Anne‐Pascale BouiniD, Sabrina LeverrieriD, S. E. Rey, S. Vorsselmans, C. Poveda Vicedo, Edwige Hiriart-Bryant, Apeksha ShapetiiD, Nicole KrönkeiD, Friedrich FeuerhakeiD, C. Hartmann, I. Petrakakis, Christiane I. OddouiD, D. Linhares, R. Cardinaels, Emmanuelle PlanusiD, S. Rocha, A. Samii, Helmut BertalanffyiD, , Eva FaurobertiD
- Citations
- 0
Abstract
Vascular disease often begins as a failure to read mechanical force. Cerebral cavernous malformations (CCMs) are leaky, brain-invading capillary clusters that cause stroke and seizures and arise from endothelial loss of the CCM complex. They form exclusively in low-flow vessels but existing models cannot explain this selectivity. We previously established that CCM-mutant endothelium inverts its adhesive balance, weakening cell-cell junctions while building matrix-degrading adhesions. The mechanosensors imposing this switch are unknown. Here we show that the mechanosensitive Ca2+ channels PIEZO1, TRPV2 and TRPV4 are overexpressed in the endothelium of CCM lesions in a 42-patient cohort, and that lesion volume scales with their expression level. Mechanistically, PIEZO1 partners with TRPV4 to destabilise cell-cell junctions and with TRPV2 to reinforce cell-matrix adhesions; silencing TRPV4 restores junctional integrity and abolishes KLF4 induction, whereas silencing TRPV2 or inhibition with tranilast abolishes matrix degradation and invasion. In vivo, trpv4 knockdown or inhibition with GSK2798745 restores atrioventricular canal morphogenesis in ccm2-mutant zebrafish. Gain of mechanosensory channel function is thus a causal step in CCM pathogenesis, upstream of the KLF program. Combined therapeutic targeting of TRPV2 and TRPV4 with inhibitors validated in humans offers a route to therapy.
- organism: mouse
- organism: zebrafish
- assay: bulk RNA-seq
- research focus: differential expression
- research focus: cell-cell communication
- research focus: drug response / drug discovery
- approach: statistical model
- approach: experimental assay
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Letting go to hold on: loss of CCM2 disrupts endothelial force balance in cerebral cavernous malformations
Sarah Vorsselmans, Samet Aytekin, … Susana Rocha·bioRxiv·Oct 16, 2026
- Integrin β1-Talin1 at focal adhesions underpin uncontrolled endothelial cell enlargement in live cerebral cavernous malformation vasculature
Mikaela S. Keyser, Teodor E. Yordanov, … Anne K. Lagendijk·bioRxiv·Nov 25, 2025
- Abortive Intussusceptive Angiogenesis Causes Multi-Cavernous Vascular Malformations
Wenqing Li, Virginia Tran, … Mark H. Ginsberg·eLifePeer-reviewed·May 20, 2021
- Force-mediated recruitment and reprogramming of healthy endothelial cells drive vascular lesion growth
A. Shapeti, J. Barrasa Fano, … H. Van Oosterwyck·bioRxiv·Nov 27, 2023
- CCM2 deficient endothelial cells undergo a mechano-dependent reprogramming into senescence associated secretory phenotype used to recruit endothelial and immune cells.
D. R. Vannier, A. Shapeti, … E. Faurobert·bioRxiv·Feb 22, 2021
- Cerebral Cavernous Malformations Develop through Clonal Expansion of Mutant Endothelial Cells
Matthew R. Detter, Daniel A. Snellings, Douglas A. Marchuk·Circulation ResearchPeer-reviewed·Oct 25, 2018