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Electrical signals in the ER are cell type and stimulus specific with extreme spatial compartmentalization in neurons
The endoplasmic reticulum (ER) is a tortuous organelle that spans throughout a cell with a continuous membrane containing ion channels, pumps, and transporters. It is unclear if stimuli that gate ER ion channels trigger substantial membrane potential fluctuations and if those fluctuations spread bey...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033362/ https://www.ncbi.nlm.nih.gov/pubmed/36640310 http://dx.doi.org/10.1016/j.celrep.2022.111943 |
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author | Campbell, Evan P. Abushawish, Ahmed A. Valdez, Lauren A. Bell, Miriam K. Haryono, Melita Rangamani, Padmini Bloodgood, Brenda L. |
author_facet | Campbell, Evan P. Abushawish, Ahmed A. Valdez, Lauren A. Bell, Miriam K. Haryono, Melita Rangamani, Padmini Bloodgood, Brenda L. |
author_sort | Campbell, Evan P. |
collection | PubMed |
description | The endoplasmic reticulum (ER) is a tortuous organelle that spans throughout a cell with a continuous membrane containing ion channels, pumps, and transporters. It is unclear if stimuli that gate ER ion channels trigger substantial membrane potential fluctuations and if those fluctuations spread beyond their site of origin. Here, we visualize ER membrane potential dynamics in HEK cells and cultured rat hippocampal neurons by targeting a genetically encoded voltage indicator specifically to the ER membrane. We report the existence of clear cell-type- and stimulus-specific ER membrane potential fluctuations. In neurons, direct stimulation of ER ryanodine receptors generates depolarizations that scale linearly with stimulus strength and reach tens of millivolts. However, ER potentials do not spread beyond the site of receptor activation, exhibiting steep attenuation that is exacerbated by intracellular large conductance K(+) channels. Thus, segments of ER can generate large depolarizations that are actively restricted from impacting nearby, contiguous membrane. |
format | Online Article Text |
id | pubmed-10033362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-100333622023-03-23 Electrical signals in the ER are cell type and stimulus specific with extreme spatial compartmentalization in neurons Campbell, Evan P. Abushawish, Ahmed A. Valdez, Lauren A. Bell, Miriam K. Haryono, Melita Rangamani, Padmini Bloodgood, Brenda L. Cell Rep Article The endoplasmic reticulum (ER) is a tortuous organelle that spans throughout a cell with a continuous membrane containing ion channels, pumps, and transporters. It is unclear if stimuli that gate ER ion channels trigger substantial membrane potential fluctuations and if those fluctuations spread beyond their site of origin. Here, we visualize ER membrane potential dynamics in HEK cells and cultured rat hippocampal neurons by targeting a genetically encoded voltage indicator specifically to the ER membrane. We report the existence of clear cell-type- and stimulus-specific ER membrane potential fluctuations. In neurons, direct stimulation of ER ryanodine receptors generates depolarizations that scale linearly with stimulus strength and reach tens of millivolts. However, ER potentials do not spread beyond the site of receptor activation, exhibiting steep attenuation that is exacerbated by intracellular large conductance K(+) channels. Thus, segments of ER can generate large depolarizations that are actively restricted from impacting nearby, contiguous membrane. 2023-01-31 2023-01-05 /pmc/articles/PMC10033362/ /pubmed/36640310 http://dx.doi.org/10.1016/j.celrep.2022.111943 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Campbell, Evan P. Abushawish, Ahmed A. Valdez, Lauren A. Bell, Miriam K. Haryono, Melita Rangamani, Padmini Bloodgood, Brenda L. Electrical signals in the ER are cell type and stimulus specific with extreme spatial compartmentalization in neurons |
title | Electrical signals in the ER are cell type and stimulus specific with extreme spatial compartmentalization in neurons |
title_full | Electrical signals in the ER are cell type and stimulus specific with extreme spatial compartmentalization in neurons |
title_fullStr | Electrical signals in the ER are cell type and stimulus specific with extreme spatial compartmentalization in neurons |
title_full_unstemmed | Electrical signals in the ER are cell type and stimulus specific with extreme spatial compartmentalization in neurons |
title_short | Electrical signals in the ER are cell type and stimulus specific with extreme spatial compartmentalization in neurons |
title_sort | electrical signals in the er are cell type and stimulus specific with extreme spatial compartmentalization in neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033362/ https://www.ncbi.nlm.nih.gov/pubmed/36640310 http://dx.doi.org/10.1016/j.celrep.2022.111943 |
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