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The ultrastructural organization of endoplasmic reticulum-plasma membrane contacts is conserved in epithelial cells
Contacts between the endoplasmic reticulum and the plasma membrane (ER-PM contacts) have important roles in membrane lipid and calcium dynamics, yet their organization in polarized epithelial cells has not been thoroughly described. Here we examine ER-PM contacts in hepatocytes in mouse liver using...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635291/ https://www.ncbi.nlm.nih.gov/pubmed/35947498 http://dx.doi.org/10.1091/mbc.E21-11-0534-T |
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author | Chung, Gary Hong Chun Lorvellec, Maëlle Gissen, Paul Pichaud, Franck Burden, Jemima J. Stefan, Christopher J. |
author_facet | Chung, Gary Hong Chun Lorvellec, Maëlle Gissen, Paul Pichaud, Franck Burden, Jemima J. Stefan, Christopher J. |
author_sort | Chung, Gary Hong Chun |
collection | PubMed |
description | Contacts between the endoplasmic reticulum and the plasma membrane (ER-PM contacts) have important roles in membrane lipid and calcium dynamics, yet their organization in polarized epithelial cells has not been thoroughly described. Here we examine ER-PM contacts in hepatocytes in mouse liver using electron microscopy, providing the first comprehensive ultrastructural study of ER-PM contacts in a mammalian epithelial tissue. Our quantitative analyses reveal strikingly distinct ER-PM contact architectures spatially linked to apical, lateral, and basal PM domains. Notably, we find that an extensive network of ER-PM contacts exists at lateral PM domains that form intercellular junctions between hepatocytes. Moreover, the spatial organization of ER-PM contacts is conserved in epithelial spheroids, suggesting that ER-PM contacts may serve conserved roles in epithelial cell architecture. Consistent with this notion, we show that ORP5 activity at ER-PM contacts modulates the apical-basolateral aspect ratio in HepG2 cells. Thus ER-PM contacts have a conserved distribution and crucial roles in PM domain architecture across epithelial cell types. |
format | Online Article Text |
id | pubmed-9635291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-96352912022-12-07 The ultrastructural organization of endoplasmic reticulum-plasma membrane contacts is conserved in epithelial cells Chung, Gary Hong Chun Lorvellec, Maëlle Gissen, Paul Pichaud, Franck Burden, Jemima J. Stefan, Christopher J. Mol Biol Cell Articles Contacts between the endoplasmic reticulum and the plasma membrane (ER-PM contacts) have important roles in membrane lipid and calcium dynamics, yet their organization in polarized epithelial cells has not been thoroughly described. Here we examine ER-PM contacts in hepatocytes in mouse liver using electron microscopy, providing the first comprehensive ultrastructural study of ER-PM contacts in a mammalian epithelial tissue. Our quantitative analyses reveal strikingly distinct ER-PM contact architectures spatially linked to apical, lateral, and basal PM domains. Notably, we find that an extensive network of ER-PM contacts exists at lateral PM domains that form intercellular junctions between hepatocytes. Moreover, the spatial organization of ER-PM contacts is conserved in epithelial spheroids, suggesting that ER-PM contacts may serve conserved roles in epithelial cell architecture. Consistent with this notion, we show that ORP5 activity at ER-PM contacts modulates the apical-basolateral aspect ratio in HepG2 cells. Thus ER-PM contacts have a conserved distribution and crucial roles in PM domain architecture across epithelial cell types. The American Society for Cell Biology 2022-09-22 /pmc/articles/PMC9635291/ /pubmed/35947498 http://dx.doi.org/10.1091/mbc.E21-11-0534-T Text en © 2022 Chung et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/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 4.0 International Creative Commons License. |
spellingShingle | Articles Chung, Gary Hong Chun Lorvellec, Maëlle Gissen, Paul Pichaud, Franck Burden, Jemima J. Stefan, Christopher J. The ultrastructural organization of endoplasmic reticulum-plasma membrane contacts is conserved in epithelial cells |
title | The ultrastructural organization of endoplasmic reticulum-plasma membrane contacts is conserved in epithelial cells |
title_full | The ultrastructural organization of endoplasmic reticulum-plasma membrane contacts is conserved in epithelial cells |
title_fullStr | The ultrastructural organization of endoplasmic reticulum-plasma membrane contacts is conserved in epithelial cells |
title_full_unstemmed | The ultrastructural organization of endoplasmic reticulum-plasma membrane contacts is conserved in epithelial cells |
title_short | The ultrastructural organization of endoplasmic reticulum-plasma membrane contacts is conserved in epithelial cells |
title_sort | ultrastructural organization of endoplasmic reticulum-plasma membrane contacts is conserved in epithelial cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635291/ https://www.ncbi.nlm.nih.gov/pubmed/35947498 http://dx.doi.org/10.1091/mbc.E21-11-0534-T |
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