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Caveolin-1 and cavin1 act synergistically to generate a unique lipid environment in caveolae

Caveolae are specialized domains of the vertebrate cell surface with a well-defined morphology and crucial roles in cell migration and mechanoprotection. Unique compositions of proteins and lipids determine membrane architectures. The precise caveolar lipid profile and the roles of the major caveola...

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Autores principales: Zhou, Yong, Ariotti, Nicholas, Rae, James, Liang, Hong, Tillu, Vikas, Tee, Shern, Bastiani, Michele, Bademosi, Adekunle T., Collins, Brett M., Meunier, Frederic A., Hancock, John F., Parton, Robert G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844427/
https://www.ncbi.nlm.nih.gov/pubmed/33496726
http://dx.doi.org/10.1083/jcb.202005138
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author Zhou, Yong
Ariotti, Nicholas
Rae, James
Liang, Hong
Tillu, Vikas
Tee, Shern
Bastiani, Michele
Bademosi, Adekunle T.
Collins, Brett M.
Meunier, Frederic A.
Hancock, John F.
Parton, Robert G.
author_facet Zhou, Yong
Ariotti, Nicholas
Rae, James
Liang, Hong
Tillu, Vikas
Tee, Shern
Bastiani, Michele
Bademosi, Adekunle T.
Collins, Brett M.
Meunier, Frederic A.
Hancock, John F.
Parton, Robert G.
author_sort Zhou, Yong
collection PubMed
description Caveolae are specialized domains of the vertebrate cell surface with a well-defined morphology and crucial roles in cell migration and mechanoprotection. Unique compositions of proteins and lipids determine membrane architectures. The precise caveolar lipid profile and the roles of the major caveolar structural proteins, caveolins and cavins, in selectively sorting lipids have not been defined. Here, we used quantitative nanoscale lipid mapping together with molecular dynamic simulations to define the caveolar lipid profile. We show that caveolin-1 (CAV1) and cavin1 individually sort distinct plasma membrane lipids. Intact caveolar structures composed of both CAV1 and cavin1 further generate a unique lipid nano-environment. The caveolar lipid sorting capability includes selectivities for lipid headgroups and acyl chains. Because lipid headgroup metabolism and acyl chain remodeling are tightly regulated, this selective lipid sorting may allow caveolae to act as transit hubs to direct communications among lipid metabolism, vesicular trafficking, and signaling.
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spelling pubmed-78444272021-09-01 Caveolin-1 and cavin1 act synergistically to generate a unique lipid environment in caveolae Zhou, Yong Ariotti, Nicholas Rae, James Liang, Hong Tillu, Vikas Tee, Shern Bastiani, Michele Bademosi, Adekunle T. Collins, Brett M. Meunier, Frederic A. Hancock, John F. Parton, Robert G. J Cell Biol Article Caveolae are specialized domains of the vertebrate cell surface with a well-defined morphology and crucial roles in cell migration and mechanoprotection. Unique compositions of proteins and lipids determine membrane architectures. The precise caveolar lipid profile and the roles of the major caveolar structural proteins, caveolins and cavins, in selectively sorting lipids have not been defined. Here, we used quantitative nanoscale lipid mapping together with molecular dynamic simulations to define the caveolar lipid profile. We show that caveolin-1 (CAV1) and cavin1 individually sort distinct plasma membrane lipids. Intact caveolar structures composed of both CAV1 and cavin1 further generate a unique lipid nano-environment. The caveolar lipid sorting capability includes selectivities for lipid headgroups and acyl chains. Because lipid headgroup metabolism and acyl chain remodeling are tightly regulated, this selective lipid sorting may allow caveolae to act as transit hubs to direct communications among lipid metabolism, vesicular trafficking, and signaling. Rockefeller University Press 2021-01-26 /pmc/articles/PMC7844427/ /pubmed/33496726 http://dx.doi.org/10.1083/jcb.202005138 Text en © 2021 Zhou et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Zhou, Yong
Ariotti, Nicholas
Rae, James
Liang, Hong
Tillu, Vikas
Tee, Shern
Bastiani, Michele
Bademosi, Adekunle T.
Collins, Brett M.
Meunier, Frederic A.
Hancock, John F.
Parton, Robert G.
Caveolin-1 and cavin1 act synergistically to generate a unique lipid environment in caveolae
title Caveolin-1 and cavin1 act synergistically to generate a unique lipid environment in caveolae
title_full Caveolin-1 and cavin1 act synergistically to generate a unique lipid environment in caveolae
title_fullStr Caveolin-1 and cavin1 act synergistically to generate a unique lipid environment in caveolae
title_full_unstemmed Caveolin-1 and cavin1 act synergistically to generate a unique lipid environment in caveolae
title_short Caveolin-1 and cavin1 act synergistically to generate a unique lipid environment in caveolae
title_sort caveolin-1 and cavin1 act synergistically to generate a unique lipid environment in caveolae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844427/
https://www.ncbi.nlm.nih.gov/pubmed/33496726
http://dx.doi.org/10.1083/jcb.202005138
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