XB-ART-46345Cell. September 28, 2012; 151 (1): 111-22.
TMEM16F forms a Ca2+-activated cation channel required for lipid scrambling in platelets during blood coagulation.
Collapse of membrane lipid asymmetry is a hallmark of blood coagulation. TMEM16F of the TMEM16 family that includes TMEM16A/B Ca(2+)-activated Cl(-) channels (CaCCs) is linked to Scott syndrome with deficient Ca(2+)-dependent lipid scrambling. We generated TMEM16F knockout mice that exhibit bleeding defects and protection in an arterial thrombosis model associated with platelet deficiency in Ca(2+)-dependent phosphatidylserine exposure and procoagulant activity and lack a Ca(2+)-activated cation current in the platelet precursor megakaryocytes. Heterologous expression of TMEM16F generates a small-conductance Ca(2+)-activated nonselective cation (SCAN) current with subpicosiemens single-channel conductance rather than a CaCC. TMEM16F-SCAN channels permeate both monovalent and divalent cations, including Ca(2+), and exhibit synergistic gating by Ca(2+) and voltage. We further pinpointed a residue in the putative pore region important for the cation versus anion selectivity of TMEM16F-SCAN and TMEM16A-CaCC channels. This study thus identifies a Ca(2+)-activated channel permeable to Ca(2+) and critical for Ca(2+)-dependent scramblase activity during blood coagulation. PAPERFLICK:
PubMed ID: 23021219
PMC ID: PMC3582364
Article link: Cell.
Grant support: HL65185 NHLBI NIH HHS , MH65334 NIMH NIH HHS, R01 HL065185 NHLBI NIH HHS , R01 NS069229 NINDS NIH HHS , R37 MH065334 NIMH NIH HHS, HL65185 NHLBI NIH HHS , R01 HL065185 NHLBI NIH HHS , R01 NS069229 NINDS NIH HHS , MH65334 NIMH NIH HHS, R01 MH065334 NIMH NIH HHS, R37 MH065334 NIMH NIH HHS
Genes referenced: ano1 ano6 clca1