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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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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. |
format | Online Article Text |
id | pubmed-5593531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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