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Plasma membrane domains enriched in cortical endoplasmic reticulum function as membrane protein trafficking hubs
In mammalian cells, the cortical endoplasmic reticulum (cER) is a network of tubules and cisterns that lie in close apposition to the plasma membrane (PM). We provide evidence that PM domains enriched in underlying cER function as trafficking hubs for insertion and removal of PM proteins in HEK 293...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756922/ https://www.ncbi.nlm.nih.gov/pubmed/23864710 http://dx.doi.org/10.1091/mbc.E12-12-0895 |
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author | Fox, Philip D. Haberkorn, Christopher J. Weigel, Aubrey V. Higgins, Jenny L. Akin, Elizabeth J. Kennedy, Matthew J. Krapf, Diego Tamkun, Michael M. |
author_facet | Fox, Philip D. Haberkorn, Christopher J. Weigel, Aubrey V. Higgins, Jenny L. Akin, Elizabeth J. Kennedy, Matthew J. Krapf, Diego Tamkun, Michael M. |
author_sort | Fox, Philip D. |
collection | PubMed |
description | In mammalian cells, the cortical endoplasmic reticulum (cER) is a network of tubules and cisterns that lie in close apposition to the plasma membrane (PM). We provide evidence that PM domains enriched in underlying cER function as trafficking hubs for insertion and removal of PM proteins in HEK 293 cells. By simultaneously visualizing cER and various transmembrane protein cargoes with total internal reflectance fluorescence microscopy, we demonstrate that the majority of exocytotic delivery events for a recycled membrane protein or for a membrane protein being delivered to the PM for the first time occur at regions enriched in cER. Likewise, we observed recurring clathrin clusters and functional endocytosis of PM proteins preferentially at the cER-enriched regions. Thus the cER network serves to organize the molecular machinery for both insertion and removal of cell surface proteins, highlighting a novel role for these unique cellular microdomains in membrane trafficking. |
format | Online Article Text |
id | pubmed-3756922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-37569222013-11-16 Plasma membrane domains enriched in cortical endoplasmic reticulum function as membrane protein trafficking hubs Fox, Philip D. Haberkorn, Christopher J. Weigel, Aubrey V. Higgins, Jenny L. Akin, Elizabeth J. Kennedy, Matthew J. Krapf, Diego Tamkun, Michael M. Mol Biol Cell Articles In mammalian cells, the cortical endoplasmic reticulum (cER) is a network of tubules and cisterns that lie in close apposition to the plasma membrane (PM). We provide evidence that PM domains enriched in underlying cER function as trafficking hubs for insertion and removal of PM proteins in HEK 293 cells. By simultaneously visualizing cER and various transmembrane protein cargoes with total internal reflectance fluorescence microscopy, we demonstrate that the majority of exocytotic delivery events for a recycled membrane protein or for a membrane protein being delivered to the PM for the first time occur at regions enriched in cER. Likewise, we observed recurring clathrin clusters and functional endocytosis of PM proteins preferentially at the cER-enriched regions. Thus the cER network serves to organize the molecular machinery for both insertion and removal of cell surface proteins, highlighting a novel role for these unique cellular microdomains in membrane trafficking. The American Society for Cell Biology 2013-09-01 /pmc/articles/PMC3756922/ /pubmed/23864710 http://dx.doi.org/10.1091/mbc.E12-12-0895 Text en © 2013 Fox et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Fox, Philip D. Haberkorn, Christopher J. Weigel, Aubrey V. Higgins, Jenny L. Akin, Elizabeth J. Kennedy, Matthew J. Krapf, Diego Tamkun, Michael M. Plasma membrane domains enriched in cortical endoplasmic reticulum function as membrane protein trafficking hubs |
title | Plasma membrane domains enriched in cortical endoplasmic reticulum function as membrane protein trafficking hubs |
title_full | Plasma membrane domains enriched in cortical endoplasmic reticulum function as membrane protein trafficking hubs |
title_fullStr | Plasma membrane domains enriched in cortical endoplasmic reticulum function as membrane protein trafficking hubs |
title_full_unstemmed | Plasma membrane domains enriched in cortical endoplasmic reticulum function as membrane protein trafficking hubs |
title_short | Plasma membrane domains enriched in cortical endoplasmic reticulum function as membrane protein trafficking hubs |
title_sort | plasma membrane domains enriched in cortical endoplasmic reticulum function as membrane protein trafficking hubs |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3756922/ https://www.ncbi.nlm.nih.gov/pubmed/23864710 http://dx.doi.org/10.1091/mbc.E12-12-0895 |
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