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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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 |
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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 |
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