G Aditya Kumar, Yousef Bagheri, Manojkumar A Puthenveedu
{"title":"膜序调节网格蛋白包覆坑动力学,但不调节起始。","authors":"G Aditya Kumar, Yousef Bagheri, Manojkumar A Puthenveedu","doi":"10.1091/mbc.E25-02-0081","DOIUrl":null,"url":null,"abstract":"<p><p>Clathrin-mediated endocytosis involves the remodeling of membranes via the initiation, maturation, and scission of clathrin-coated pits (CCPs). How CCP initiation and dynamics are regulated has been addressed primarily from the perspective of the core proteins that mediate endocytosis. Whether and how the physical properties of the membrane regulate CCP initiation and dynamics are heavily underexplored. Here, we used a solvatochromic probe to readout membrane order in the plasma membrane in live cells undergoing endocytosis, using total internal reflection fluorescence microscopy. Cholesterol depletion decreased membrane order, and reduced CCP initiation and increased lifetimes of CCPs. In unperturbed cells, however, membrane order was correlated to CCP lifetimes, but not their initiation. When membrane order was decreased or increased independently without extracting lipids, CCP lifetimes were affected, but CCP initiation was not. Together, by reading out membrane order in living cells undergoing endocytosis and manipulating membrane order in both directions, we show that membrane order primarily regulates CCP dynamics, and that cholesterol extraction has additional effects on CCP initiation independent of its effect on order.</p>","PeriodicalId":18735,"journal":{"name":"Molecular Biology of the Cell","volume":" ","pages":"br17"},"PeriodicalIF":2.7000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12260180/pdf/","citationCount":"0","resultStr":"{\"title\":\"Membrane order regulates clathrin-coated pit dynamics but not initiation.\",\"authors\":\"G Aditya Kumar, Yousef Bagheri, Manojkumar A Puthenveedu\",\"doi\":\"10.1091/mbc.E25-02-0081\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Clathrin-mediated endocytosis involves the remodeling of membranes via the initiation, maturation, and scission of clathrin-coated pits (CCPs). How CCP initiation and dynamics are regulated has been addressed primarily from the perspective of the core proteins that mediate endocytosis. Whether and how the physical properties of the membrane regulate CCP initiation and dynamics are heavily underexplored. Here, we used a solvatochromic probe to readout membrane order in the plasma membrane in live cells undergoing endocytosis, using total internal reflection fluorescence microscopy. Cholesterol depletion decreased membrane order, and reduced CCP initiation and increased lifetimes of CCPs. In unperturbed cells, however, membrane order was correlated to CCP lifetimes, but not their initiation. When membrane order was decreased or increased independently without extracting lipids, CCP lifetimes were affected, but CCP initiation was not. Together, by reading out membrane order in living cells undergoing endocytosis and manipulating membrane order in both directions, we show that membrane order primarily regulates CCP dynamics, and that cholesterol extraction has additional effects on CCP initiation independent of its effect on order.</p>\",\"PeriodicalId\":18735,\"journal\":{\"name\":\"Molecular Biology of the Cell\",\"volume\":\" \",\"pages\":\"br17\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12260180/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Biology of the Cell\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1091/mbc.E25-02-0081\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/4/30 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Biology of the Cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1091/mbc.E25-02-0081","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/30 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
Membrane order regulates clathrin-coated pit dynamics but not initiation.
Clathrin-mediated endocytosis involves the remodeling of membranes via the initiation, maturation, and scission of clathrin-coated pits (CCPs). How CCP initiation and dynamics are regulated has been addressed primarily from the perspective of the core proteins that mediate endocytosis. Whether and how the physical properties of the membrane regulate CCP initiation and dynamics are heavily underexplored. Here, we used a solvatochromic probe to readout membrane order in the plasma membrane in live cells undergoing endocytosis, using total internal reflection fluorescence microscopy. Cholesterol depletion decreased membrane order, and reduced CCP initiation and increased lifetimes of CCPs. In unperturbed cells, however, membrane order was correlated to CCP lifetimes, but not their initiation. When membrane order was decreased or increased independently without extracting lipids, CCP lifetimes were affected, but CCP initiation was not. Together, by reading out membrane order in living cells undergoing endocytosis and manipulating membrane order in both directions, we show that membrane order primarily regulates CCP dynamics, and that cholesterol extraction has additional effects on CCP initiation independent of its effect on order.
期刊介绍:
MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.