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IP(3) receptor isoforms differently regulate ER-mitochondrial contacts and local calcium transfer
Contact sites of endoplasmic reticulum (ER) and mitochondria locally convey calcium signals between the IP(3) receptors (IP3R) and the mitochondrial calcium uniporter, and are central to cell survival. It remains unclear whether IP3Rs also have a structural role in contact formation and whether the...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700175/ https://www.ncbi.nlm.nih.gov/pubmed/31427578 http://dx.doi.org/10.1038/s41467-019-11646-3 |
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author | Bartok, Adam Weaver, David Golenár, Tünde Nichtova, Zuzana Katona, Máté Bánsághi, Száva Alzayady, Kamil J. Thomas, V. Kaye Ando, Hideaki Mikoshiba, Katsuhiko Joseph, Suresh K. Yule, David I. Csordás, György Hajnóczky, György |
author_facet | Bartok, Adam Weaver, David Golenár, Tünde Nichtova, Zuzana Katona, Máté Bánsághi, Száva Alzayady, Kamil J. Thomas, V. Kaye Ando, Hideaki Mikoshiba, Katsuhiko Joseph, Suresh K. Yule, David I. Csordás, György Hajnóczky, György |
author_sort | Bartok, Adam |
collection | PubMed |
description | Contact sites of endoplasmic reticulum (ER) and mitochondria locally convey calcium signals between the IP(3) receptors (IP3R) and the mitochondrial calcium uniporter, and are central to cell survival. It remains unclear whether IP3Rs also have a structural role in contact formation and whether the different IP3R isoforms have redundant functions. Using an IP3R-deficient cell model rescued with each of the three IP3R isoforms and an array of super-resolution and ultrastructural approaches we demonstrate that IP3Rs are required for maintaining ER-mitochondrial contacts. This role is independent of calcium fluxes. We also show that, while each isoform can support contacts, type 2 IP3R is the most effective in delivering calcium to the mitochondria. Thus, these studies reveal a non-canonical, structural role for the IP3Rs and direct attention towards the type 2 IP3R that was previously neglected in the context of ER-mitochondrial calcium signaling. |
format | Online Article Text |
id | pubmed-6700175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67001752019-08-21 IP(3) receptor isoforms differently regulate ER-mitochondrial contacts and local calcium transfer Bartok, Adam Weaver, David Golenár, Tünde Nichtova, Zuzana Katona, Máté Bánsághi, Száva Alzayady, Kamil J. Thomas, V. Kaye Ando, Hideaki Mikoshiba, Katsuhiko Joseph, Suresh K. Yule, David I. Csordás, György Hajnóczky, György Nat Commun Article Contact sites of endoplasmic reticulum (ER) and mitochondria locally convey calcium signals between the IP(3) receptors (IP3R) and the mitochondrial calcium uniporter, and are central to cell survival. It remains unclear whether IP3Rs also have a structural role in contact formation and whether the different IP3R isoforms have redundant functions. Using an IP3R-deficient cell model rescued with each of the three IP3R isoforms and an array of super-resolution and ultrastructural approaches we demonstrate that IP3Rs are required for maintaining ER-mitochondrial contacts. This role is independent of calcium fluxes. We also show that, while each isoform can support contacts, type 2 IP3R is the most effective in delivering calcium to the mitochondria. Thus, these studies reveal a non-canonical, structural role for the IP3Rs and direct attention towards the type 2 IP3R that was previously neglected in the context of ER-mitochondrial calcium signaling. Nature Publishing Group UK 2019-08-19 /pmc/articles/PMC6700175/ /pubmed/31427578 http://dx.doi.org/10.1038/s41467-019-11646-3 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Bartok, Adam Weaver, David Golenár, Tünde Nichtova, Zuzana Katona, Máté Bánsághi, Száva Alzayady, Kamil J. Thomas, V. Kaye Ando, Hideaki Mikoshiba, Katsuhiko Joseph, Suresh K. Yule, David I. Csordás, György Hajnóczky, György IP(3) receptor isoforms differently regulate ER-mitochondrial contacts and local calcium transfer |
title | IP(3) receptor isoforms differently regulate ER-mitochondrial contacts and local calcium transfer |
title_full | IP(3) receptor isoforms differently regulate ER-mitochondrial contacts and local calcium transfer |
title_fullStr | IP(3) receptor isoforms differently regulate ER-mitochondrial contacts and local calcium transfer |
title_full_unstemmed | IP(3) receptor isoforms differently regulate ER-mitochondrial contacts and local calcium transfer |
title_short | IP(3) receptor isoforms differently regulate ER-mitochondrial contacts and local calcium transfer |
title_sort | ip(3) receptor isoforms differently regulate er-mitochondrial contacts and local calcium transfer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700175/ https://www.ncbi.nlm.nih.gov/pubmed/31427578 http://dx.doi.org/10.1038/s41467-019-11646-3 |
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