Cargando…
Ceramide structure dictates glycosphingolipid nanodomain assembly and function
Gangliosides in the outer leaflet of the plasma membrane of eukaryotic cells are essential for many cellular functions and pathogenic interactions. How gangliosides are dynamically organized and how they respond to ligand binding is poorly understood. Using fluorescence anisotropy imaging of synthet...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209009/ https://www.ncbi.nlm.nih.gov/pubmed/34135326 http://dx.doi.org/10.1038/s41467-021-23961-9 |
_version_ | 1783709038770388992 |
---|---|
author | Arumugam, Senthil Schmieder, Stefanie Pezeshkian, Weria Becken, Ulrike Wunder, Christian Chinnapen, Dan Ipsen, John Hjort Kenworthy, Anne K. Lencer, Wayne Mayor, Satyajit Johannes, Ludger |
author_facet | Arumugam, Senthil Schmieder, Stefanie Pezeshkian, Weria Becken, Ulrike Wunder, Christian Chinnapen, Dan Ipsen, John Hjort Kenworthy, Anne K. Lencer, Wayne Mayor, Satyajit Johannes, Ludger |
author_sort | Arumugam, Senthil |
collection | PubMed |
description | Gangliosides in the outer leaflet of the plasma membrane of eukaryotic cells are essential for many cellular functions and pathogenic interactions. How gangliosides are dynamically organized and how they respond to ligand binding is poorly understood. Using fluorescence anisotropy imaging of synthetic, fluorescently labeled GM1 gangliosides incorporated into the plasma membrane of living cells, we found that GM1 with a fully saturated C16:0 acyl chain, but not with unsaturated C16:1 acyl chain, is actively clustered into nanodomains, which depends on membrane cholesterol, phosphatidylserine and actin. The binding of cholera toxin B-subunit (CTxB) leads to enlarged membrane domains for both C16:0 and C16:1, owing to binding of multiple GM1 under a toxin, and clustering of CTxB. The structure of the ceramide acyl chain still affects these domains, as co-clustering with the glycosylphosphatidylinositol (GPI)-anchored protein CD59 occurs only when GM1 contains the fully saturated C16:0 acyl chain, and not C16:1. Thus, different ceramide species of GM1 gangliosides dictate their assembly into nanodomains and affect nanodomain structure and function, which likely underlies many endogenous cellular processes. |
format | Online Article Text |
id | pubmed-8209009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82090092021-07-01 Ceramide structure dictates glycosphingolipid nanodomain assembly and function Arumugam, Senthil Schmieder, Stefanie Pezeshkian, Weria Becken, Ulrike Wunder, Christian Chinnapen, Dan Ipsen, John Hjort Kenworthy, Anne K. Lencer, Wayne Mayor, Satyajit Johannes, Ludger Nat Commun Article Gangliosides in the outer leaflet of the plasma membrane of eukaryotic cells are essential for many cellular functions and pathogenic interactions. How gangliosides are dynamically organized and how they respond to ligand binding is poorly understood. Using fluorescence anisotropy imaging of synthetic, fluorescently labeled GM1 gangliosides incorporated into the plasma membrane of living cells, we found that GM1 with a fully saturated C16:0 acyl chain, but not with unsaturated C16:1 acyl chain, is actively clustered into nanodomains, which depends on membrane cholesterol, phosphatidylserine and actin. The binding of cholera toxin B-subunit (CTxB) leads to enlarged membrane domains for both C16:0 and C16:1, owing to binding of multiple GM1 under a toxin, and clustering of CTxB. The structure of the ceramide acyl chain still affects these domains, as co-clustering with the glycosylphosphatidylinositol (GPI)-anchored protein CD59 occurs only when GM1 contains the fully saturated C16:0 acyl chain, and not C16:1. Thus, different ceramide species of GM1 gangliosides dictate their assembly into nanodomains and affect nanodomain structure and function, which likely underlies many endogenous cellular processes. Nature Publishing Group UK 2021-06-16 /pmc/articles/PMC8209009/ /pubmed/34135326 http://dx.doi.org/10.1038/s41467-021-23961-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Arumugam, Senthil Schmieder, Stefanie Pezeshkian, Weria Becken, Ulrike Wunder, Christian Chinnapen, Dan Ipsen, John Hjort Kenworthy, Anne K. Lencer, Wayne Mayor, Satyajit Johannes, Ludger Ceramide structure dictates glycosphingolipid nanodomain assembly and function |
title | Ceramide structure dictates glycosphingolipid nanodomain assembly and function |
title_full | Ceramide structure dictates glycosphingolipid nanodomain assembly and function |
title_fullStr | Ceramide structure dictates glycosphingolipid nanodomain assembly and function |
title_full_unstemmed | Ceramide structure dictates glycosphingolipid nanodomain assembly and function |
title_short | Ceramide structure dictates glycosphingolipid nanodomain assembly and function |
title_sort | ceramide structure dictates glycosphingolipid nanodomain assembly and function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209009/ https://www.ncbi.nlm.nih.gov/pubmed/34135326 http://dx.doi.org/10.1038/s41467-021-23961-9 |
work_keys_str_mv | AT arumugamsenthil ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction AT schmiederstefanie ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction AT pezeshkianweria ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction AT beckenulrike ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction AT wunderchristian ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction AT chinnapendan ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction AT ipsenjohnhjort ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction AT kenworthyannek ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction AT lencerwayne ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction AT mayorsatyajit ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction AT johannesludger ceramidestructuredictatesglycosphingolipidnanodomainassemblyandfunction |