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CamelliA-based simultaneous imaging of Ca(2+) dynamics in subcellular compartments
As a universal second messenger, calcium (Ca(2+)) transmits specific cellular signals via a spatiotemporal signature generated from its extracellular source and internal stores. Our knowledge of the mechanisms underlying the generation of a Ca(2+) signature is hampered by limited tools for simultane...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968278/ https://www.ncbi.nlm.nih.gov/pubmed/35218352 http://dx.doi.org/10.1093/plphys/kiac020 |
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author | Guo, Jingzhe He, Jiangman Dehesh, Katayoon Cui, Xinping Yang, Zhenbiao |
author_facet | Guo, Jingzhe He, Jiangman Dehesh, Katayoon Cui, Xinping Yang, Zhenbiao |
author_sort | Guo, Jingzhe |
collection | PubMed |
description | As a universal second messenger, calcium (Ca(2+)) transmits specific cellular signals via a spatiotemporal signature generated from its extracellular source and internal stores. Our knowledge of the mechanisms underlying the generation of a Ca(2+) signature is hampered by limited tools for simultaneously monitoring dynamic Ca(2+) levels in multiple subcellular compartments. To overcome the limitation and to further improve spatiotemporal resolutions, we have assembled a molecular toolset (CamelliA lines) in Arabidopsis (Arabidopsis thaliana) that enables simultaneous and high-resolution monitoring of Ca(2+) dynamics in multiple subcellular compartments through imaging different single-colored genetically encoded calcium indicators. We uncovered several Ca(2+) signatures in three types of Arabidopsis cells in response to internal and external cues, including rapid oscillations of cytosolic Ca(2+) and apical plasma membrane Ca(2+) influx in fast-growing Arabidopsis pollen tubes, the spatiotemporal relationship of Ca(2+) dynamics in four subcellular compartments of root epidermal cells challenged with salt, and a shockwave-like Ca(2+) wave propagating in laser-wounded leaf epidermis. These observations serve as a testimony to the wide applicability of the CamelliA lines for elucidating the subcellular sources contributing to the Ca(2+) signatures in plants. |
format | Online Article Text |
id | pubmed-8968278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-89682782022-03-31 CamelliA-based simultaneous imaging of Ca(2+) dynamics in subcellular compartments Guo, Jingzhe He, Jiangman Dehesh, Katayoon Cui, Xinping Yang, Zhenbiao Plant Physiol Regular Issue Content As a universal second messenger, calcium (Ca(2+)) transmits specific cellular signals via a spatiotemporal signature generated from its extracellular source and internal stores. Our knowledge of the mechanisms underlying the generation of a Ca(2+) signature is hampered by limited tools for simultaneously monitoring dynamic Ca(2+) levels in multiple subcellular compartments. To overcome the limitation and to further improve spatiotemporal resolutions, we have assembled a molecular toolset (CamelliA lines) in Arabidopsis (Arabidopsis thaliana) that enables simultaneous and high-resolution monitoring of Ca(2+) dynamics in multiple subcellular compartments through imaging different single-colored genetically encoded calcium indicators. We uncovered several Ca(2+) signatures in three types of Arabidopsis cells in response to internal and external cues, including rapid oscillations of cytosolic Ca(2+) and apical plasma membrane Ca(2+) influx in fast-growing Arabidopsis pollen tubes, the spatiotemporal relationship of Ca(2+) dynamics in four subcellular compartments of root epidermal cells challenged with salt, and a shockwave-like Ca(2+) wave propagating in laser-wounded leaf epidermis. These observations serve as a testimony to the wide applicability of the CamelliA lines for elucidating the subcellular sources contributing to the Ca(2+) signatures in plants. Oxford University Press 2022-02-26 /pmc/articles/PMC8968278/ /pubmed/35218352 http://dx.doi.org/10.1093/plphys/kiac020 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Regular Issue Content Guo, Jingzhe He, Jiangman Dehesh, Katayoon Cui, Xinping Yang, Zhenbiao CamelliA-based simultaneous imaging of Ca(2+) dynamics in subcellular compartments |
title | CamelliA-based simultaneous imaging of Ca(2+) dynamics in subcellular compartments |
title_full | CamelliA-based simultaneous imaging of Ca(2+) dynamics in subcellular compartments |
title_fullStr | CamelliA-based simultaneous imaging of Ca(2+) dynamics in subcellular compartments |
title_full_unstemmed | CamelliA-based simultaneous imaging of Ca(2+) dynamics in subcellular compartments |
title_short | CamelliA-based simultaneous imaging of Ca(2+) dynamics in subcellular compartments |
title_sort | camellia-based simultaneous imaging of ca(2+) dynamics in subcellular compartments |
topic | Regular Issue Content |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968278/ https://www.ncbi.nlm.nih.gov/pubmed/35218352 http://dx.doi.org/10.1093/plphys/kiac020 |
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