Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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
_version_ 1783444813965688832
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
work_keys_str_mv AT bartokadam ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT weaverdavid ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT golenartunde ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT nichtovazuzana ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT katonamate ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT bansaghiszava ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT alzayadykamilj ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT thomasvkaye ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT andohideaki ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT mikoshibakatsuhiko ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT josephsureshk ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT yuledavidi ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT csordasgyorgy ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer
AT hajnoczkygyorgy ip3receptorisoformsdifferentlyregulateermitochondrialcontactsandlocalcalciumtransfer