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Long-term monitoring of Ca(2+) dynamics in C. elegans pharynx: an in vivo energy balance sensor

Ca(2+) is a key signal transducer for muscle contraction. Continuous in vivo monitoring of intracellular Ca(2+)-dynamics in C. elegans pharynx muscle revealed surprisingly complex Ca(2+) patterns. Despite the age-dependent decline of pharynx pumping, we observed unaltered fast Ca(2+) oscillations bo...

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Autores principales: Alvarez-Illera, Pilar, Sanchez-Blanco, Adolfo, Lopez-Burillo, Silvia, Fonteriz, Rosalba I., Alvarez, Javier, Montero, Mayte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356515/
https://www.ncbi.nlm.nih.gov/pubmed/27661127
http://dx.doi.org/10.18632/oncotarget.12177
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author Alvarez-Illera, Pilar
Sanchez-Blanco, Adolfo
Lopez-Burillo, Silvia
Fonteriz, Rosalba I.
Alvarez, Javier
Montero, Mayte
author_facet Alvarez-Illera, Pilar
Sanchez-Blanco, Adolfo
Lopez-Burillo, Silvia
Fonteriz, Rosalba I.
Alvarez, Javier
Montero, Mayte
author_sort Alvarez-Illera, Pilar
collection PubMed
description Ca(2+) is a key signal transducer for muscle contraction. Continuous in vivo monitoring of intracellular Ca(2+)-dynamics in C. elegans pharynx muscle revealed surprisingly complex Ca(2+) patterns. Despite the age-dependent decline of pharynx pumping, we observed unaltered fast Ca(2+) oscillations both in young and old worms. In addition, sporadic prolonged Ca(2+) increases lasting many seconds or minutes were often observed in between periods of fast Ca(2+) oscillations. We attribute them to the inhibition of ATP-dependent Ca(2+)-pumps upon energy depletion. Accordingly, food deprivation largely augmented the frequency of prolonged [Ca(2+)] increases. However, paradoxically, prolonged [Ca(2+)] increases were more frequently observed in young worms than in older ones, and less frequently observed in energy-deficient mitochondrial respiratory chain nuo-6 mutants than in wild-type controls. We hypothesize that young animals are more susceptible to energy depletion due to their faster energy consumption rate, while nuo-6 mutants may keep better the energy balance by slowing energy consumption. Our data therefore suggest that the metabolic state of the pharynx during feeding stimulation depends mainly on the delicate balance between the instant rates of energy production and consumption. Thus, in vivo monitoring of muscle Ca(2+) dynamics can be used as a novel tool to study cellular energy availability.
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spelling pubmed-53565152017-03-24 Long-term monitoring of Ca(2+) dynamics in C. elegans pharynx: an in vivo energy balance sensor Alvarez-Illera, Pilar Sanchez-Blanco, Adolfo Lopez-Burillo, Silvia Fonteriz, Rosalba I. Alvarez, Javier Montero, Mayte Oncotarget Research Paper: Gerotarget (Focus on Aging) Ca(2+) is a key signal transducer for muscle contraction. Continuous in vivo monitoring of intracellular Ca(2+)-dynamics in C. elegans pharynx muscle revealed surprisingly complex Ca(2+) patterns. Despite the age-dependent decline of pharynx pumping, we observed unaltered fast Ca(2+) oscillations both in young and old worms. In addition, sporadic prolonged Ca(2+) increases lasting many seconds or minutes were often observed in between periods of fast Ca(2+) oscillations. We attribute them to the inhibition of ATP-dependent Ca(2+)-pumps upon energy depletion. Accordingly, food deprivation largely augmented the frequency of prolonged [Ca(2+)] increases. However, paradoxically, prolonged [Ca(2+)] increases were more frequently observed in young worms than in older ones, and less frequently observed in energy-deficient mitochondrial respiratory chain nuo-6 mutants than in wild-type controls. We hypothesize that young animals are more susceptible to energy depletion due to their faster energy consumption rate, while nuo-6 mutants may keep better the energy balance by slowing energy consumption. Our data therefore suggest that the metabolic state of the pharynx during feeding stimulation depends mainly on the delicate balance between the instant rates of energy production and consumption. Thus, in vivo monitoring of muscle Ca(2+) dynamics can be used as a novel tool to study cellular energy availability. Impact Journals LLC 2016-09-21 /pmc/articles/PMC5356515/ /pubmed/27661127 http://dx.doi.org/10.18632/oncotarget.12177 Text en Copyright: © 2016 Alvarez-Illera et al. http://creativecommons.org/licenses/by/3.0/ 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 credited.
spellingShingle Research Paper: Gerotarget (Focus on Aging)
Alvarez-Illera, Pilar
Sanchez-Blanco, Adolfo
Lopez-Burillo, Silvia
Fonteriz, Rosalba I.
Alvarez, Javier
Montero, Mayte
Long-term monitoring of Ca(2+) dynamics in C. elegans pharynx: an in vivo energy balance sensor
title Long-term monitoring of Ca(2+) dynamics in C. elegans pharynx: an in vivo energy balance sensor
title_full Long-term monitoring of Ca(2+) dynamics in C. elegans pharynx: an in vivo energy balance sensor
title_fullStr Long-term monitoring of Ca(2+) dynamics in C. elegans pharynx: an in vivo energy balance sensor
title_full_unstemmed Long-term monitoring of Ca(2+) dynamics in C. elegans pharynx: an in vivo energy balance sensor
title_short Long-term monitoring of Ca(2+) dynamics in C. elegans pharynx: an in vivo energy balance sensor
title_sort long-term monitoring of ca(2+) dynamics in c. elegans pharynx: an in vivo energy balance sensor
topic Research Paper: Gerotarget (Focus on Aging)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356515/
https://www.ncbi.nlm.nih.gov/pubmed/27661127
http://dx.doi.org/10.18632/oncotarget.12177
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