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Pharynx mitochondrial [Ca(2+)] dynamics in live C. elegans worms during aging

Progressive decline in mitochondrial function is generally considered one of the hallmarks of aging. We have expressed a Ca(2+) sensor in the mitochondrial matrix of C. elegans pharynx cells and we have measured for the first time mitochondrial [Ca(2+)] ([Ca(2+)](M)) dynamics in the pharynx of live...

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Autores principales: Alvarez-Illera, Pilar, García-Casas, Paloma, Arias-del-Val, Jessica, Fonteriz, Rosalba I., Alvarez, Javier, Montero, Mayte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593531/
https://www.ncbi.nlm.nih.gov/pubmed/28915560
http://dx.doi.org/10.18632/oncotarget.18600
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author Alvarez-Illera, Pilar
García-Casas, Paloma
Arias-del-Val, Jessica
Fonteriz, Rosalba I.
Alvarez, Javier
Montero, Mayte
author_facet Alvarez-Illera, Pilar
García-Casas, Paloma
Arias-del-Val, Jessica
Fonteriz, Rosalba I.
Alvarez, Javier
Montero, Mayte
author_sort Alvarez-Illera, Pilar
collection PubMed
description Progressive decline in mitochondrial function is generally considered one of the hallmarks of aging. We have expressed a Ca(2+) sensor in the mitochondrial matrix of C. elegans pharynx cells and we have measured for the first time mitochondrial [Ca(2+)] ([Ca(2+)](M)) dynamics in the pharynx of live C. elegans worms during aging. Our results show that worms stimulated with serotonin display a pharynx [Ca(2+)](M) oscillatory kinetics that includes both high frequency oscillations (up to about 1Hz) and very prolonged “square-wave” [Ca(2+)](M) increases, indicative of energy depletion of the pharynx cells. Mitochondrial [Ca(2+)] is therefore able to follow “beat-to-beat” the fast oscillations of cytosolic [Ca(2+)]. The fast [Ca(2+)](M) oscillations kept steady frequency values during the whole worm life, from 2 to 12 days old, but the height and width of the peaks was progressively reduced. [Ca(2+)](M) oscillations were also present with similar kinetics in respiratory chain complex I nuo-6 mutant worms, although with smaller height and frequency than in the controls, and larger width. In summary, Ca(2+) fluxes in and out of the mitochondria are relatively well preserved during the C. elegans life, but there is a clear progressive decrease in their magnitude during aging. Moreover, mitochondrial Ca(2+) fluxes were smaller in nuo-6 mutants with respect to the controls at every age and decreased similarly during aging.
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spelling pubmed-55935312017-09-14 Pharynx mitochondrial [Ca(2+)] dynamics in live C. elegans worms during aging Alvarez-Illera, Pilar García-Casas, Paloma Arias-del-Val, Jessica Fonteriz, Rosalba I. Alvarez, Javier Montero, Mayte Oncotarget Research Paper: Gerotarget (Focus on Aging) Progressive decline in mitochondrial function is generally considered one of the hallmarks of aging. We have expressed a Ca(2+) sensor in the mitochondrial matrix of C. elegans pharynx cells and we have measured for the first time mitochondrial [Ca(2+)] ([Ca(2+)](M)) dynamics in the pharynx of live C. elegans worms during aging. Our results show that worms stimulated with serotonin display a pharynx [Ca(2+)](M) oscillatory kinetics that includes both high frequency oscillations (up to about 1Hz) and very prolonged “square-wave” [Ca(2+)](M) increases, indicative of energy depletion of the pharynx cells. Mitochondrial [Ca(2+)] is therefore able to follow “beat-to-beat” the fast oscillations of cytosolic [Ca(2+)]. The fast [Ca(2+)](M) oscillations kept steady frequency values during the whole worm life, from 2 to 12 days old, but the height and width of the peaks was progressively reduced. [Ca(2+)](M) oscillations were also present with similar kinetics in respiratory chain complex I nuo-6 mutant worms, although with smaller height and frequency than in the controls, and larger width. In summary, Ca(2+) fluxes in and out of the mitochondria are relatively well preserved during the C. elegans life, but there is a clear progressive decrease in their magnitude during aging. Moreover, mitochondrial Ca(2+) fluxes were smaller in nuo-6 mutants with respect to the controls at every age and decreased similarly during aging. Impact Journals LLC 2017-06-22 /pmc/articles/PMC5593531/ /pubmed/28915560 http://dx.doi.org/10.18632/oncotarget.18600 Text en Copyright: © 2017 Alvarez-Illera et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper: Gerotarget (Focus on Aging)
Alvarez-Illera, Pilar
García-Casas, Paloma
Arias-del-Val, Jessica
Fonteriz, Rosalba I.
Alvarez, Javier
Montero, Mayte
Pharynx mitochondrial [Ca(2+)] dynamics in live C. elegans worms during aging
title Pharynx mitochondrial [Ca(2+)] dynamics in live C. elegans worms during aging
title_full Pharynx mitochondrial [Ca(2+)] dynamics in live C. elegans worms during aging
title_fullStr Pharynx mitochondrial [Ca(2+)] dynamics in live C. elegans worms during aging
title_full_unstemmed Pharynx mitochondrial [Ca(2+)] dynamics in live C. elegans worms during aging
title_short Pharynx mitochondrial [Ca(2+)] dynamics in live C. elegans worms during aging
title_sort pharynx mitochondrial [ca(2+)] dynamics in live c. elegans worms during aging
topic Research Paper: Gerotarget (Focus on Aging)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593531/
https://www.ncbi.nlm.nih.gov/pubmed/28915560
http://dx.doi.org/10.18632/oncotarget.18600
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