CCM2 deficient endothelial cells undergo a mechano-dependent reprogramming into senescence associated secretory phenotype used to recruit endothelial and immune cells.

Vannier, D. R.; Shapeti, A.; Chuffart, F.; Planus, E.; Manet, S.; Rivier, P.; destaing, o.; Albiges-Rizo, C.; Van Oosterwyck, H.; Faurobert, E.

doi:10.1101/2021.02.22.432204

bioRxiv · 10.1101/2021.02.22.432204

CCM2 deficient endothelial cells undergo a mechano-dependent reprogramming into senescence associated secretory phenotype used to recruit endothelial and immune cells.

Vannier, D. R.·Shapeti, A.·Chuffart, F.·Planus, E.·Manet, S.·Rivier, P.·destaing, o.·Albiges-Rizo, C.·Van Oosterwyck, H.·Faurobert, E.

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Abstract

Cerebral Cavernous Malformations (CCM) is a cerebrovascular disease in which stacks of dilated haemorrhagic capillaries form focally in the brain. Whether and how defective mechanotransduction, cellular mosaicism and inflammation interplay to sustain the progression of CCM diseases is unknown. Here, we reveal that CCM1- and CCM2-silenced endothelial cells enter into senescence associated with secretory phenotype (SASP) that they use to invade the extracellular matrix and attract surrounding wild-type endothelial and immune cells. Further, we demonstrate that this SASP is driven by the mechanical and molecular disorders provoked by ROCKs dysfunctions. By this, we identify CCM1/2 and ROCKs as parts of a scaffold controlling senescence, bringing new insights into the emerging field of the control of aging by cellular mechanics. This discovery reconciles the dysregulated traits of CCM1/2-deficient endothelial cells into a unique mechano-dependent endothelial fate that links perturbed mechanics to microenvironment remodelling and long-range activation of endothelial and immune cells.

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Vannier, D. R., Shapeti, A., Chuffart, F., Planus, E., Manet, S., Rivier, P., destaing, o., Albiges-Rizo, C., Van Oosterwyck, H., Faurobert, E.. 2021-02-22. CCM2 deficient endothelial cells undergo a mechano-dependent reprogramming into senescence associated secretory phenotype used to recruit endothelial and immune cells.. https://doi.org/10.1101/2021.02.22.432204

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