Cargando…

Mitochondrial Mg(2+) homeostasis decides cellular energy metabolism and vulnerability to stress

Cellular energy production processes are composed of many Mg(2+) dependent enzymatic reactions. In fact, dysregulation of Mg(2+) homeostasis is involved in various cellular malfunctions and diseases. Recently, mitochondria, energy-producing organelles, have been known as major intracellular Mg(2+) s...

Descripción completa

Detalles Bibliográficos
Autores principales: Yamanaka, Ryu, Tabata, Sho, Shindo, Yutaka, Hotta, Kohji, Suzuki, Koji, Soga, Tomoyoshi, Oka, Kotaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960558/
https://www.ncbi.nlm.nih.gov/pubmed/27458051
http://dx.doi.org/10.1038/srep30027
_version_ 1782444545328283648
author Yamanaka, Ryu
Tabata, Sho
Shindo, Yutaka
Hotta, Kohji
Suzuki, Koji
Soga, Tomoyoshi
Oka, Kotaro
author_facet Yamanaka, Ryu
Tabata, Sho
Shindo, Yutaka
Hotta, Kohji
Suzuki, Koji
Soga, Tomoyoshi
Oka, Kotaro
author_sort Yamanaka, Ryu
collection PubMed
description Cellular energy production processes are composed of many Mg(2+) dependent enzymatic reactions. In fact, dysregulation of Mg(2+) homeostasis is involved in various cellular malfunctions and diseases. Recently, mitochondria, energy-producing organelles, have been known as major intracellular Mg(2+) stores. Several biological stimuli alter mitochondrial Mg(2+) concentration by intracellular redistribution. However, in living cells, whether mitochondrial Mg(2+) alteration affect cellular energy metabolism remains unclear. Mg(2+) transporter of mitochondrial inner membrane MRS2 is an essential component of mitochondrial Mg(2+) uptake system. Here, we comprehensively analyzed intracellular Mg(2+) levels and energy metabolism in Mrs2 knockdown (KD) cells using fluorescence imaging and metabolome analysis. Dysregulation of mitochondrial Mg(2+) homeostasis disrupted ATP production via shift of mitochondrial energy metabolism and morphology. Moreover, Mrs2 KD sensitized cellular tolerance against cellular stress. These results indicate regulation of mitochondrial Mg(2+) via MRS2 critically decides cellular energy status and cell vulnerability via regulation of mitochondrial Mg(2+) level in response to physiological stimuli.
format Online
Article
Text
id pubmed-4960558
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-49605582016-08-05 Mitochondrial Mg(2+) homeostasis decides cellular energy metabolism and vulnerability to stress Yamanaka, Ryu Tabata, Sho Shindo, Yutaka Hotta, Kohji Suzuki, Koji Soga, Tomoyoshi Oka, Kotaro Sci Rep Article Cellular energy production processes are composed of many Mg(2+) dependent enzymatic reactions. In fact, dysregulation of Mg(2+) homeostasis is involved in various cellular malfunctions and diseases. Recently, mitochondria, energy-producing organelles, have been known as major intracellular Mg(2+) stores. Several biological stimuli alter mitochondrial Mg(2+) concentration by intracellular redistribution. However, in living cells, whether mitochondrial Mg(2+) alteration affect cellular energy metabolism remains unclear. Mg(2+) transporter of mitochondrial inner membrane MRS2 is an essential component of mitochondrial Mg(2+) uptake system. Here, we comprehensively analyzed intracellular Mg(2+) levels and energy metabolism in Mrs2 knockdown (KD) cells using fluorescence imaging and metabolome analysis. Dysregulation of mitochondrial Mg(2+) homeostasis disrupted ATP production via shift of mitochondrial energy metabolism and morphology. Moreover, Mrs2 KD sensitized cellular tolerance against cellular stress. These results indicate regulation of mitochondrial Mg(2+) via MRS2 critically decides cellular energy status and cell vulnerability via regulation of mitochondrial Mg(2+) level in response to physiological stimuli. Nature Publishing Group 2016-07-26 /pmc/articles/PMC4960558/ /pubmed/27458051 http://dx.doi.org/10.1038/srep30027 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yamanaka, Ryu
Tabata, Sho
Shindo, Yutaka
Hotta, Kohji
Suzuki, Koji
Soga, Tomoyoshi
Oka, Kotaro
Mitochondrial Mg(2+) homeostasis decides cellular energy metabolism and vulnerability to stress
title Mitochondrial Mg(2+) homeostasis decides cellular energy metabolism and vulnerability to stress
title_full Mitochondrial Mg(2+) homeostasis decides cellular energy metabolism and vulnerability to stress
title_fullStr Mitochondrial Mg(2+) homeostasis decides cellular energy metabolism and vulnerability to stress
title_full_unstemmed Mitochondrial Mg(2+) homeostasis decides cellular energy metabolism and vulnerability to stress
title_short Mitochondrial Mg(2+) homeostasis decides cellular energy metabolism and vulnerability to stress
title_sort mitochondrial mg(2+) homeostasis decides cellular energy metabolism and vulnerability to stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960558/
https://www.ncbi.nlm.nih.gov/pubmed/27458051
http://dx.doi.org/10.1038/srep30027
work_keys_str_mv AT yamanakaryu mitochondrialmg2homeostasisdecidescellularenergymetabolismandvulnerabilitytostress
AT tabatasho mitochondrialmg2homeostasisdecidescellularenergymetabolismandvulnerabilitytostress
AT shindoyutaka mitochondrialmg2homeostasisdecidescellularenergymetabolismandvulnerabilitytostress
AT hottakohji mitochondrialmg2homeostasisdecidescellularenergymetabolismandvulnerabilitytostress
AT suzukikoji mitochondrialmg2homeostasisdecidescellularenergymetabolismandvulnerabilitytostress
AT sogatomoyoshi mitochondrialmg2homeostasisdecidescellularenergymetabolismandvulnerabilitytostress
AT okakotaro mitochondrialmg2homeostasisdecidescellularenergymetabolismandvulnerabilitytostress