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Newly Developed Mg(2+)–Selective Fluorescent Probe Enables Visualization of Mg(2+) Dynamics in Mitochondria

Mg(2+) plays important roles in numerous cellular functions. Mitochondria take part in intracellular Mg(2+) regulation and the Mg(2+) concentration in mitochondria affects the synthesis of ATP. However, there are few methods to observe Mg(2+) in mitochondria in intact cells. Here, we have developed...

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Autores principales: Shindo, Yutaka, Fujii, Tomohiko, Komatsu, Hirokazu, Citterio, Daniel, Hotta, Kohji, Suzuki, Koji, Oka, Kotaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156752/
https://www.ncbi.nlm.nih.gov/pubmed/21858208
http://dx.doi.org/10.1371/journal.pone.0023684
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author Shindo, Yutaka
Fujii, Tomohiko
Komatsu, Hirokazu
Citterio, Daniel
Hotta, Kohji
Suzuki, Koji
Oka, Kotaro
author_facet Shindo, Yutaka
Fujii, Tomohiko
Komatsu, Hirokazu
Citterio, Daniel
Hotta, Kohji
Suzuki, Koji
Oka, Kotaro
author_sort Shindo, Yutaka
collection PubMed
description Mg(2+) plays important roles in numerous cellular functions. Mitochondria take part in intracellular Mg(2+) regulation and the Mg(2+) concentration in mitochondria affects the synthesis of ATP. However, there are few methods to observe Mg(2+) in mitochondria in intact cells. Here, we have developed a novel Mg(2+)–selective fluorescent probe, KMG-301, that is functional in mitochondria. This probe changes its fluorescence properties solely depending on the Mg(2+) concentration in mitochondria under physiologically normal conditions. Simultaneous measurements using this probe together with a probe for cytosolic Mg(2+), KMG-104, enabled us to compare the dynamics of Mg(2+) in the cytosol and in mitochondria. With this method, carbonyl cyanide p-(trifluoromethoxy) phenylhydrazone (FCCP)–induced Mg(2+) mobilization from mitochondria to the cytosol was visualized. Although a FCCP–induced decrease in the Mg(2+) concentration in mitochondria and an increase in the cytosol were observed both in differentiated PC12 cells and in hippocampal neurons, the time-courses of concentration changes varied with cell type. Moreover, the relationship between mitochondrial Mg(2+) and Parkinson's disease was analyzed in a cellular model of Parkinson's disease by using the 1-methyl-4-phenylpyridinium ion (MPP(+)). A gradual decrease in the Mg(2+) concentration in mitochondria was observed in response to MPP(+) in differentiated PC12 cells. These results indicate that KMG-301 is useful for investigating Mg(2+) dynamics in mitochondria. All animal procedures to obtain neurons from Wistar rats were approved by the ethical committee of Keio University (permit number is 09106-(1)).
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spelling pubmed-31567522011-08-19 Newly Developed Mg(2+)–Selective Fluorescent Probe Enables Visualization of Mg(2+) Dynamics in Mitochondria Shindo, Yutaka Fujii, Tomohiko Komatsu, Hirokazu Citterio, Daniel Hotta, Kohji Suzuki, Koji Oka, Kotaro PLoS One Research Article Mg(2+) plays important roles in numerous cellular functions. Mitochondria take part in intracellular Mg(2+) regulation and the Mg(2+) concentration in mitochondria affects the synthesis of ATP. However, there are few methods to observe Mg(2+) in mitochondria in intact cells. Here, we have developed a novel Mg(2+)–selective fluorescent probe, KMG-301, that is functional in mitochondria. This probe changes its fluorescence properties solely depending on the Mg(2+) concentration in mitochondria under physiologically normal conditions. Simultaneous measurements using this probe together with a probe for cytosolic Mg(2+), KMG-104, enabled us to compare the dynamics of Mg(2+) in the cytosol and in mitochondria. With this method, carbonyl cyanide p-(trifluoromethoxy) phenylhydrazone (FCCP)–induced Mg(2+) mobilization from mitochondria to the cytosol was visualized. Although a FCCP–induced decrease in the Mg(2+) concentration in mitochondria and an increase in the cytosol were observed both in differentiated PC12 cells and in hippocampal neurons, the time-courses of concentration changes varied with cell type. Moreover, the relationship between mitochondrial Mg(2+) and Parkinson's disease was analyzed in a cellular model of Parkinson's disease by using the 1-methyl-4-phenylpyridinium ion (MPP(+)). A gradual decrease in the Mg(2+) concentration in mitochondria was observed in response to MPP(+) in differentiated PC12 cells. These results indicate that KMG-301 is useful for investigating Mg(2+) dynamics in mitochondria. All animal procedures to obtain neurons from Wistar rats were approved by the ethical committee of Keio University (permit number is 09106-(1)). Public Library of Science 2011-08-16 /pmc/articles/PMC3156752/ /pubmed/21858208 http://dx.doi.org/10.1371/journal.pone.0023684 Text en Shindo et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shindo, Yutaka
Fujii, Tomohiko
Komatsu, Hirokazu
Citterio, Daniel
Hotta, Kohji
Suzuki, Koji
Oka, Kotaro
Newly Developed Mg(2+)–Selective Fluorescent Probe Enables Visualization of Mg(2+) Dynamics in Mitochondria
title Newly Developed Mg(2+)–Selective Fluorescent Probe Enables Visualization of Mg(2+) Dynamics in Mitochondria
title_full Newly Developed Mg(2+)–Selective Fluorescent Probe Enables Visualization of Mg(2+) Dynamics in Mitochondria
title_fullStr Newly Developed Mg(2+)–Selective Fluorescent Probe Enables Visualization of Mg(2+) Dynamics in Mitochondria
title_full_unstemmed Newly Developed Mg(2+)–Selective Fluorescent Probe Enables Visualization of Mg(2+) Dynamics in Mitochondria
title_short Newly Developed Mg(2+)–Selective Fluorescent Probe Enables Visualization of Mg(2+) Dynamics in Mitochondria
title_sort newly developed mg(2+)–selective fluorescent probe enables visualization of mg(2+) dynamics in mitochondria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156752/
https://www.ncbi.nlm.nih.gov/pubmed/21858208
http://dx.doi.org/10.1371/journal.pone.0023684
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