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Shaped by leaky ER: Homeostatic Ca(2+) fluxes

At any moment in time, cells coordinate and balance their calcium ion (Ca(2+)) fluxes. The term ‘Ca(2+) homeostasis’ suggests that balancing resting Ca(2+) levels is a rather static process. However, direct ER Ca(2+) imaging shows that resting Ca(2+) levels are maintained by surprisingly dynamic Ca(...

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Detalles Bibliográficos
Autores principales: Schulte, Annemarie, Blum, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491824/
https://www.ncbi.nlm.nih.gov/pubmed/36160838
http://dx.doi.org/10.3389/fphys.2022.972104
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author Schulte, Annemarie
Blum, Robert
author_facet Schulte, Annemarie
Blum, Robert
author_sort Schulte, Annemarie
collection PubMed
description At any moment in time, cells coordinate and balance their calcium ion (Ca(2+)) fluxes. The term ‘Ca(2+) homeostasis’ suggests that balancing resting Ca(2+) levels is a rather static process. However, direct ER Ca(2+) imaging shows that resting Ca(2+) levels are maintained by surprisingly dynamic Ca(2+) fluxes between the ER Ca(2+) store, the cytosol, and the extracellular space. The data show that the ER Ca(2+) leak, continuously fed by the high-energy consuming SERCA, is a fundamental driver of resting Ca(2+) dynamics. Based on simplistic Ca(2+) toolkit models, we discuss how the ER Ca(2+) leak could contribute to evolutionarily conserved Ca(2+) phenomena such as Ca(2+) entry, ER Ca(2+) release, and Ca(2+) oscillations.
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spelling pubmed-94918242022-09-22 Shaped by leaky ER: Homeostatic Ca(2+) fluxes Schulte, Annemarie Blum, Robert Front Physiol Physiology At any moment in time, cells coordinate and balance their calcium ion (Ca(2+)) fluxes. The term ‘Ca(2+) homeostasis’ suggests that balancing resting Ca(2+) levels is a rather static process. However, direct ER Ca(2+) imaging shows that resting Ca(2+) levels are maintained by surprisingly dynamic Ca(2+) fluxes between the ER Ca(2+) store, the cytosol, and the extracellular space. The data show that the ER Ca(2+) leak, continuously fed by the high-energy consuming SERCA, is a fundamental driver of resting Ca(2+) dynamics. Based on simplistic Ca(2+) toolkit models, we discuss how the ER Ca(2+) leak could contribute to evolutionarily conserved Ca(2+) phenomena such as Ca(2+) entry, ER Ca(2+) release, and Ca(2+) oscillations. Frontiers Media S.A. 2022-09-07 /pmc/articles/PMC9491824/ /pubmed/36160838 http://dx.doi.org/10.3389/fphys.2022.972104 Text en Copyright © 2022 Schulte and Blum. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Schulte, Annemarie
Blum, Robert
Shaped by leaky ER: Homeostatic Ca(2+) fluxes
title Shaped by leaky ER: Homeostatic Ca(2+) fluxes
title_full Shaped by leaky ER: Homeostatic Ca(2+) fluxes
title_fullStr Shaped by leaky ER: Homeostatic Ca(2+) fluxes
title_full_unstemmed Shaped by leaky ER: Homeostatic Ca(2+) fluxes
title_short Shaped by leaky ER: Homeostatic Ca(2+) fluxes
title_sort shaped by leaky er: homeostatic ca(2+) fluxes
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491824/
https://www.ncbi.nlm.nih.gov/pubmed/36160838
http://dx.doi.org/10.3389/fphys.2022.972104
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