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Red fluorescent CEPIA indicators for visualization of Ca(2+) dynamics in mitochondria
Mitochondrial Ca(2+) dynamics are involved in the regulation of multifarious cellular processes, including intracellular Ca(2+) signalling, cell metabolism and cell death. Use of mitochondria-targeted genetically encoded Ca(2+) indicators has revealed intercellular and subcellular heterogeneity of m...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029041/ https://www.ncbi.nlm.nih.gov/pubmed/32071363 http://dx.doi.org/10.1038/s41598-020-59707-8 |
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author | Kanemaru, Kazunori Suzuki, Junji Taiko, Isamu Iino, Masamitsu |
author_facet | Kanemaru, Kazunori Suzuki, Junji Taiko, Isamu Iino, Masamitsu |
author_sort | Kanemaru, Kazunori |
collection | PubMed |
description | Mitochondrial Ca(2+) dynamics are involved in the regulation of multifarious cellular processes, including intracellular Ca(2+) signalling, cell metabolism and cell death. Use of mitochondria-targeted genetically encoded Ca(2+) indicators has revealed intercellular and subcellular heterogeneity of mitochondrial Ca(2+) dynamics, which are assumed to be determined by distinct thresholds of Ca(2+) increases at each subcellular mitochondrial domain. The balance between Ca(2+) influx through the mitochondrial calcium uniporter and extrusion by cation exchangers across the inner mitochondrial membrane may define the threshold; however, the precise mechanisms remain to be further explored. We here report the new red fluorescent genetically encoded Ca(2+) indicators, R-CEPIA3mt and R-CEPIA4mt, which are targeted to mitochondria and their Ca(2+) affinities are engineered to match the intramitochondrial Ca(2+) concentrations. They enable visualization of mitochondrial Ca(2+) dynamics with high spatiotemporal resolution in parallel with the use of green fluorescent probes and optogenetic tools. Thus, R-CEPIA3mt and R-CEPIA4mt are expected to be a useful tool for elucidating the mechanisms of the complex mitochondrial Ca(2+) dynamics and their functions. |
format | Online Article Text |
id | pubmed-7029041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70290412020-02-26 Red fluorescent CEPIA indicators for visualization of Ca(2+) dynamics in mitochondria Kanemaru, Kazunori Suzuki, Junji Taiko, Isamu Iino, Masamitsu Sci Rep Article Mitochondrial Ca(2+) dynamics are involved in the regulation of multifarious cellular processes, including intracellular Ca(2+) signalling, cell metabolism and cell death. Use of mitochondria-targeted genetically encoded Ca(2+) indicators has revealed intercellular and subcellular heterogeneity of mitochondrial Ca(2+) dynamics, which are assumed to be determined by distinct thresholds of Ca(2+) increases at each subcellular mitochondrial domain. The balance between Ca(2+) influx through the mitochondrial calcium uniporter and extrusion by cation exchangers across the inner mitochondrial membrane may define the threshold; however, the precise mechanisms remain to be further explored. We here report the new red fluorescent genetically encoded Ca(2+) indicators, R-CEPIA3mt and R-CEPIA4mt, which are targeted to mitochondria and their Ca(2+) affinities are engineered to match the intramitochondrial Ca(2+) concentrations. They enable visualization of mitochondrial Ca(2+) dynamics with high spatiotemporal resolution in parallel with the use of green fluorescent probes and optogenetic tools. Thus, R-CEPIA3mt and R-CEPIA4mt are expected to be a useful tool for elucidating the mechanisms of the complex mitochondrial Ca(2+) dynamics and their functions. Nature Publishing Group UK 2020-02-18 /pmc/articles/PMC7029041/ /pubmed/32071363 http://dx.doi.org/10.1038/s41598-020-59707-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kanemaru, Kazunori Suzuki, Junji Taiko, Isamu Iino, Masamitsu Red fluorescent CEPIA indicators for visualization of Ca(2+) dynamics in mitochondria |
title | Red fluorescent CEPIA indicators for visualization of Ca(2+) dynamics in mitochondria |
title_full | Red fluorescent CEPIA indicators for visualization of Ca(2+) dynamics in mitochondria |
title_fullStr | Red fluorescent CEPIA indicators for visualization of Ca(2+) dynamics in mitochondria |
title_full_unstemmed | Red fluorescent CEPIA indicators for visualization of Ca(2+) dynamics in mitochondria |
title_short | Red fluorescent CEPIA indicators for visualization of Ca(2+) dynamics in mitochondria |
title_sort | red fluorescent cepia indicators for visualization of ca(2+) dynamics in mitochondria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029041/ https://www.ncbi.nlm.nih.gov/pubmed/32071363 http://dx.doi.org/10.1038/s41598-020-59707-8 |
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