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Publication : Two types of type IV P-type ATPases independently re-establish the asymmetrical distribution of phosphatidylserine in plasma membranes.

First Author  Miyata Y Year  2022
Journal  J Biol Chem Volume  298
Issue  11 Pages  102527
PubMed ID  36162506 Mgi Jnum  J:341852
Mgi Id  MGI:7377911 Doi  10.1016/j.jbc.2022.102527
Citation  Miyata Y, et al. (2022) Two types of type IV P-type ATPases independently re-establish the asymmetrical distribution of phosphatidylserine in plasma membranes. J Biol Chem 298(11):102527
abstractText  Phospholipids are asymmetrically distributed between the lipid bilayer of plasma membranes in which phosphatidylserine (PtdSer) is confined to the inner leaflet. ATP11A and ATP11C, type IV P-Type ATPases in plasma membranes, flip PtdSer from the outer to the inner leaflet, but involvement of other P4-ATPases is unclear. We herein demonstrated that once PtdSer was exposed on the cell surface of ATP11A(-/-)ATP11C(-/-) mouse T cell line (W3), its internalization to the inner leaflet of plasma membranes was negligible at 15 degrees C. However, ATP11A(-/-)ATP11C(-/-) cells internalized the exposed PtdSer at 37 degrees C, a temperature at which trafficking of intracellular membranes was active. In addition to ATP11A and 11C, W3 cells expressed ATP8A1, 8B2, 8B4, 9A, 9B, and 11B, with ATP8A1 and ATP11B being present at recycling endosomes. Cells deficient in four P4-ATPases (ATP8A1, 11A, 11B, and 11C) (QKO) did not constitutively expose PtdSer on the cell surface but lost the ability to re-establish PtdSer asymmetry within 1 hour, even at 37 degrees C. The expression of ATP11A or ATP11C conferred QKO cells with the ability to rapidly re-establish PtdSer asymmetry at 15 degrees C and 37 degrees C, while cells expressing ATP8A1 or ATP11B required a temperature of 37 degrees C to achieve this function, and a dynamin inhibitor blocked this process. These results revealed that mammalian cells are equipped with two independent mechanisms to re-establish its asymmetry: the first is a rapid process involving plasma membrane flippases, ATP11A and ATP11C, while the other is mediated by ATP8A1 and ATP11B, which require an endocytosis process.
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