{"title":"Phosphatidylserine transport in cell life and death","authors":"Alenka {Č}opi{č}CRBM, Thibaud DieudonnéI2BC, Guillaume LenoirI2BC","doi":"arxiv-2311.05223","DOIUrl":null,"url":null,"abstract":"Phosphatidylserine (PS) is a negatively-charged glycerophospholipid found\nmainly in the plasma membrane (PM) and in the late secretory/endocytic\ncompartments, where it regulates cellular activity and can mediate apoptosis.\nExport of PS from the endoplasmic reticulum, its site of synthesis, to other\ncompartments, and its transbilayer asymmetry must therefore be precisely\nregulated. We review recent findings on non-vesicular transport of PS by lipid\ntransfer proteins (LTPs) at membrane contact sites, on PS flip-flop between\nmembrane leaflets by flippases and scramblases, and on PS nano-clustering at\nthe PM. We also discuss emerging data on cooperation between scramblases and\nLTPs, how perturbation of PS distribution can lead to disease, and the specific\nrole of PS in viral infection.","PeriodicalId":501170,"journal":{"name":"arXiv - QuanBio - Subcellular Processes","volume":"52 7","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Subcellular Processes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2311.05223","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Phosphatidylserine (PS) is a negatively-charged glycerophospholipid found
mainly in the plasma membrane (PM) and in the late secretory/endocytic
compartments, where it regulates cellular activity and can mediate apoptosis.
Export of PS from the endoplasmic reticulum, its site of synthesis, to other
compartments, and its transbilayer asymmetry must therefore be precisely
regulated. We review recent findings on non-vesicular transport of PS by lipid
transfer proteins (LTPs) at membrane contact sites, on PS flip-flop between
membrane leaflets by flippases and scramblases, and on PS nano-clustering at
the PM. We also discuss emerging data on cooperation between scramblases and
LTPs, how perturbation of PS distribution can lead to disease, and the specific
role of PS in viral infection.