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Ca(2+)-associated triphasic pH changes in mitochondria during brown adipocyte activation

OBJECTIVE: Brown adipocytes (BAs) are endowed with a high metabolic capacity for energy expenditure due to their high mitochondria content. While mitochondrial pH is dynamically regulated in response to stimulation and, in return, affects various metabolic processes, how mitochondrial pH is regulate...

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Autores principales: Hou, Yanyan, Kitaguchi, Tetsuya, Kriszt, Rókus, Tseng, Yu-Hua, Raghunath, Michael, Suzuki, Madoka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518710/
https://www.ncbi.nlm.nih.gov/pubmed/28752044
http://dx.doi.org/10.1016/j.molmet.2017.05.013
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author Hou, Yanyan
Kitaguchi, Tetsuya
Kriszt, Rókus
Tseng, Yu-Hua
Raghunath, Michael
Suzuki, Madoka
author_facet Hou, Yanyan
Kitaguchi, Tetsuya
Kriszt, Rókus
Tseng, Yu-Hua
Raghunath, Michael
Suzuki, Madoka
author_sort Hou, Yanyan
collection PubMed
description OBJECTIVE: Brown adipocytes (BAs) are endowed with a high metabolic capacity for energy expenditure due to their high mitochondria content. While mitochondrial pH is dynamically regulated in response to stimulation and, in return, affects various metabolic processes, how mitochondrial pH is regulated during adrenergic stimulation-induced thermogenesis is unknown. We aimed to reveal the spatial and temporal dynamics of mitochondrial pH in stimulated BAs and the mechanisms behind the dynamic pH changes. METHODS: A mitochondrial targeted pH-sensitive protein, mito-pHluorin, was constructed and transfected to BAs. Transfected BAs were stimulated by an adrenergic agonist, isoproterenol. The pH changes in mitochondria were characterized by dual-color imaging with indicators that monitor mitochondrial membrane potential and heat production. The mechanisms of pH changes were studied by examining the involvement of electron transport chain (ETC) activity and Ca(2+) profiles in mitochondria and the intracellular Ca(2+) store, the endoplasmic reticulum (ER). RESULTS: A triphasic mitochondrial pH change in BAs upon adrenergic stimulation was revealed. In comparison to a thermosensitive dye, we reveal that phases 1 and 2 of the pH increase precede thermogenesis, while phase 3, characterized by a pH decrease, occurs during thermogenesis. The mechanism of pH increase is partially related to ETC. In addition, the pH increase occurs concurrently with an increase in mitochondrial Ca(2+). This Ca(2+) increase is contributed to by an influx from the ER, and it is further involved in mitochondrial pH regulation. CONCLUSIONS: We demonstrate that an increase in mitochondrial pH is implicated as an early event in adrenergically stimulated BAs. We further suggest that this pH increase may play a role in the potentiation of thermogenesis.
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spelling pubmed-55187102017-07-27 Ca(2+)-associated triphasic pH changes in mitochondria during brown adipocyte activation Hou, Yanyan Kitaguchi, Tetsuya Kriszt, Rókus Tseng, Yu-Hua Raghunath, Michael Suzuki, Madoka Mol Metab Original Article OBJECTIVE: Brown adipocytes (BAs) are endowed with a high metabolic capacity for energy expenditure due to their high mitochondria content. While mitochondrial pH is dynamically regulated in response to stimulation and, in return, affects various metabolic processes, how mitochondrial pH is regulated during adrenergic stimulation-induced thermogenesis is unknown. We aimed to reveal the spatial and temporal dynamics of mitochondrial pH in stimulated BAs and the mechanisms behind the dynamic pH changes. METHODS: A mitochondrial targeted pH-sensitive protein, mito-pHluorin, was constructed and transfected to BAs. Transfected BAs were stimulated by an adrenergic agonist, isoproterenol. The pH changes in mitochondria were characterized by dual-color imaging with indicators that monitor mitochondrial membrane potential and heat production. The mechanisms of pH changes were studied by examining the involvement of electron transport chain (ETC) activity and Ca(2+) profiles in mitochondria and the intracellular Ca(2+) store, the endoplasmic reticulum (ER). RESULTS: A triphasic mitochondrial pH change in BAs upon adrenergic stimulation was revealed. In comparison to a thermosensitive dye, we reveal that phases 1 and 2 of the pH increase precede thermogenesis, while phase 3, characterized by a pH decrease, occurs during thermogenesis. The mechanism of pH increase is partially related to ETC. In addition, the pH increase occurs concurrently with an increase in mitochondrial Ca(2+). This Ca(2+) increase is contributed to by an influx from the ER, and it is further involved in mitochondrial pH regulation. CONCLUSIONS: We demonstrate that an increase in mitochondrial pH is implicated as an early event in adrenergically stimulated BAs. We further suggest that this pH increase may play a role in the potentiation of thermogenesis. Elsevier 2017-05-31 /pmc/articles/PMC5518710/ /pubmed/28752044 http://dx.doi.org/10.1016/j.molmet.2017.05.013 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Hou, Yanyan
Kitaguchi, Tetsuya
Kriszt, Rókus
Tseng, Yu-Hua
Raghunath, Michael
Suzuki, Madoka
Ca(2+)-associated triphasic pH changes in mitochondria during brown adipocyte activation
title Ca(2+)-associated triphasic pH changes in mitochondria during brown adipocyte activation
title_full Ca(2+)-associated triphasic pH changes in mitochondria during brown adipocyte activation
title_fullStr Ca(2+)-associated triphasic pH changes in mitochondria during brown adipocyte activation
title_full_unstemmed Ca(2+)-associated triphasic pH changes in mitochondria during brown adipocyte activation
title_short Ca(2+)-associated triphasic pH changes in mitochondria during brown adipocyte activation
title_sort ca(2+)-associated triphasic ph changes in mitochondria during brown adipocyte activation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518710/
https://www.ncbi.nlm.nih.gov/pubmed/28752044
http://dx.doi.org/10.1016/j.molmet.2017.05.013
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