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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(...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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. |
format | Online Article Text |
id | pubmed-9491824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT schulteannemarie shapedbyleakyerhomeostaticca2fluxes AT blumrobert shapedbyleakyerhomeostaticca2fluxes |