PIEZO1 gain-of-function mutations delay reticulocyte maturation in hereditary xerocytosis.
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ABSTRACT:
SUBMITTER: Moura PL
PROVIDER: S-EPMC7271576 | biostudies-literature | 2020 Jun
REPOSITORIES: biostudies-literature
Publications
PIEZO1 gain-of-function mutations delay reticulocyte maturation in hereditary xerocytosis.
Moura Pedro L PL Hawley Bethan R BR Dobbe Johannes G G JGG Streekstra Geert J GJ Rab Minke A E MAE Bianchi Paola P van Wijk Richard R Toye Ashley M AM Satchwell Timothy J TJ
Haematologica 20191017 6
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Project description:AbstractCell-surface exposure of phosphatidylserine (PS) is essential for phagocytic clearance and blood clotting. Although a calcium-activated phospholipid scramblase (CaPLSase) has long been proposed to mediate PS exposure in red blood cells (RBCs), its identity, activation mechanism, and role in RBC biology and disease remain elusive. Here, we demonstrate that TMEM16F, the long-sought-after RBC CaPLSase, is activated by calcium influx through the mechanosensitive channel PIEZO1 in RBCs. PIEZO1-TMEM16F functional coupling is enhanced in RBCs from individuals with hereditary xerocytosis (HX), an RBC disorder caused by PIEZO1 gain-of-function channelopathy. Enhanced PIEZO1-TMEM16F coupling leads to an increased propensity to expose PS, which may serve as a key risk factor for HX clinical manifestations including anemia, splenomegaly, and postsplenectomy thrombosis. Spider toxin GsMTx-4 and antigout medication benzbromarone inhibit PIEZO1, preventing force-induced echinocytosis, hemolysis, and PS exposure in HX RBCs. Our study thus reveals an activation mechanism of TMEM16F CaPLSase and its pathophysiological function in HX, providing insights into potential treatment.
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2023-03-11 | PXD031963 | Pride
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