ATP11A and ATP11C are plasma membrane phosphatidylserine flippases in in vitro human megakaryocytes.
Ruby M. BaxteriD, Alexi CrosbyiD, Holly R. FosteriD, Winnie W. Y. LauiD, Amie K. WalleriD, Cédric GhevaertiD, Matthew Thomas HarperiD
Abstract
Thrombotic diseases are the major worldwide cause of cardiovascular death. Platelets prevent blood loss following injury (haemostasis), but inappropriate and excessive platelet activation can lead to thrombosis. Platelet activation must be tightly controlled. Pro-coagulant platelets expose phosphatidylserine (PS), enabling coagulation complex assembly, enhancing thrombin generation and thrombosis. PS is normally restricted to the inner leaflet of the plasma membrane by flippase (aminophospholipid translocase) activity. However, the flippase protein(s) responsible for this crucial activity in platelets remains unidentified. The P4 ATPases ATP11A and ATP11C, regulated by their obligatory partner CDC50A, flip PS at the plasma membrane in a range of different cell types. To investigate platelet flippases, human induced pluripotent stem cells (hiPSCs) were forward-programmed into CD41+/CD42+ megakaryocytes, the platelet precursor. Wildtype (WT) forward-programmed megakaryocytes showed similar flippase activity to human platelets with internalisation of NBD-PS that could be inhibited by high cytosolic Ca2+ or N-ethylmaleimide (NEM). We then generated CDC50A, ATP11A or ATP11C single knockout and ATP11A/11C double knockout (DKO) hiPSCs using CRISPR-Cas9. CDC50A-KO, ATP11A-KO, ATP11C-KO and DKO hiPSC clones successfully formed CD41a+/CD42a+ mature megakaryocytes. CDC50A-KO megakaryocytes bound Annexin V when unstimulated and had no remaining NEM-sensitive flippase activity indicating the involvement of a P4-ATPase. Although ATP11A-KO and ATP11C-KO megakaryocytes had similar flippase activity to WT clones, DKO clones had inhibited NBD-PS internalisation compared to WT and had no remaining NEM-sensitive flippase activity. This indicates that the CDC50A-regulated P4-ATPases ATP11A and ATP11C act together at the megakaryocyte plasma membrane and are responsible for PS flippase activity and therefore likely responsible in human platelets.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
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
- Cyclin-dependent kinase 2 (Cdk2) controls phosphatase-regulated signaling and function in platelets
Paul R. Woods, Brian L. Hood, … Richard A. Steinman·bioRxiv·May 31, 2020
- Sodium/Potassium ATPase Alpha 1 Subunit Fine-tunes Platelet GPCR Signaling Function and is Essential for Thrombosis
Oliver Q Li, Yue Hong, … Wei Li·bioRxiv·May 13, 2024
- The intracellular and plasma membrane pools of PI4P control megakaryocyte maturation and proplatelet formation
A. Bura, A. Jurak Begonja·bioRxiv·Jul 28, 2022
- Notch signaling functions in non-canonical juxtacrine manner in platelets to amplify thrombogenicity
S. N. Chaurasia, M. Ekhlak, … D. Dash·bioRxiv·May 6, 2022
- RAP1-RHO small GTPase cross-talk mediates integrin-dependent and -independent platelet procoagulant response
Abigail Ballard-Kordeliski, Nikola Ziegmann, … Wolfgang Bergmeier·HaematologicaPeer-reviewed·Mar 5, 2026
- CRISPR/Cas9-mediated deletion of Shp1 and Shp2 reveals distinct roles in human megakaryopoiesis and proplatelet formation
Eugénie Schaeffer, Elsa Barré, … Alexandra Mazharian·bioRxiv·Jul 24, 2026