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Determination of protoplast growth properties using quantitative single-cell tracking analysis

BACKGROUND: Although quantitative single-cell analysis is frequently applied in animal systems, e.g. to identify novel drugs, similar applications on plant single cells are largely missing. We have exploited the applicability of high-throughput microscopic image analysis on plant single cells using...

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Autores principales: Dawson, Jonathan, Pandey, Saurabh, Yu, Qiuju, Schaub, Patrick, Wüst, Florian, Moradi, Amir Bahram, Dovzhenko, Oleksandr, Palme, Klaus, Welsch, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118701/
https://www.ncbi.nlm.nih.gov/pubmed/35585602
http://dx.doi.org/10.1186/s13007-022-00895-x
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author Dawson, Jonathan
Pandey, Saurabh
Yu, Qiuju
Schaub, Patrick
Wüst, Florian
Moradi, Amir Bahram
Dovzhenko, Oleksandr
Palme, Klaus
Welsch, Ralf
author_facet Dawson, Jonathan
Pandey, Saurabh
Yu, Qiuju
Schaub, Patrick
Wüst, Florian
Moradi, Amir Bahram
Dovzhenko, Oleksandr
Palme, Klaus
Welsch, Ralf
author_sort Dawson, Jonathan
collection PubMed
description BACKGROUND: Although quantitative single-cell analysis is frequently applied in animal systems, e.g. to identify novel drugs, similar applications on plant single cells are largely missing. We have exploited the applicability of high-throughput microscopic image analysis on plant single cells using tobacco leaf protoplasts, cell-wall free single cells isolated by lytic digestion. Protoplasts regenerate their cell wall within several days after isolation and have the potential to expand and proliferate, generating microcalli and finally whole plants after the application of suitable regeneration conditions. RESULTS: High-throughput automated microscopy coupled with the development of image processing pipelines allowed to quantify various developmental properties of thousands of protoplasts during the initial days following cultivation by immobilization in multi-well-plates. The focus on early protoplast responses allowed to study cell expansion prior to the initiation of proliferation and without the effects of shape-compromising cell walls. We compared growth parameters of wild-type tobacco cells with cells expressing the antiapoptotic protein Bcl2-associated athanogene 4 from Arabidopsis (AtBAG4). CONCLUSIONS: AtBAG4-expressing protoplasts showed a higher proportion of cells responding with positive area increases than the wild type and showed increased growth rates as well as increased proliferation rates upon continued cultivation. These features are associated with reported observations on a BAG4-mediated increased resilience to various stress responses and improved cellular survival rates following transformation approaches. Moreover, our single-cell expansion results suggest a BAG4-mediated, cell-independent increase of potassium channel abundance which was hitherto reported for guard cells only. The possibility to explain plant phenotypes with single-cell properties, extracted with the single-cell processing and analysis pipeline developed, allows to envision novel biotechnological screening strategies able to determine improved plant properties via single-cell analysis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-022-00895-x.
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spelling pubmed-91187012022-05-20 Determination of protoplast growth properties using quantitative single-cell tracking analysis Dawson, Jonathan Pandey, Saurabh Yu, Qiuju Schaub, Patrick Wüst, Florian Moradi, Amir Bahram Dovzhenko, Oleksandr Palme, Klaus Welsch, Ralf Plant Methods Research BACKGROUND: Although quantitative single-cell analysis is frequently applied in animal systems, e.g. to identify novel drugs, similar applications on plant single cells are largely missing. We have exploited the applicability of high-throughput microscopic image analysis on plant single cells using tobacco leaf protoplasts, cell-wall free single cells isolated by lytic digestion. Protoplasts regenerate their cell wall within several days after isolation and have the potential to expand and proliferate, generating microcalli and finally whole plants after the application of suitable regeneration conditions. RESULTS: High-throughput automated microscopy coupled with the development of image processing pipelines allowed to quantify various developmental properties of thousands of protoplasts during the initial days following cultivation by immobilization in multi-well-plates. The focus on early protoplast responses allowed to study cell expansion prior to the initiation of proliferation and without the effects of shape-compromising cell walls. We compared growth parameters of wild-type tobacco cells with cells expressing the antiapoptotic protein Bcl2-associated athanogene 4 from Arabidopsis (AtBAG4). CONCLUSIONS: AtBAG4-expressing protoplasts showed a higher proportion of cells responding with positive area increases than the wild type and showed increased growth rates as well as increased proliferation rates upon continued cultivation. These features are associated with reported observations on a BAG4-mediated increased resilience to various stress responses and improved cellular survival rates following transformation approaches. Moreover, our single-cell expansion results suggest a BAG4-mediated, cell-independent increase of potassium channel abundance which was hitherto reported for guard cells only. The possibility to explain plant phenotypes with single-cell properties, extracted with the single-cell processing and analysis pipeline developed, allows to envision novel biotechnological screening strategies able to determine improved plant properties via single-cell analysis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-022-00895-x. BioMed Central 2022-05-18 /pmc/articles/PMC9118701/ /pubmed/35585602 http://dx.doi.org/10.1186/s13007-022-00895-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Dawson, Jonathan
Pandey, Saurabh
Yu, Qiuju
Schaub, Patrick
Wüst, Florian
Moradi, Amir Bahram
Dovzhenko, Oleksandr
Palme, Klaus
Welsch, Ralf
Determination of protoplast growth properties using quantitative single-cell tracking analysis
title Determination of protoplast growth properties using quantitative single-cell tracking analysis
title_full Determination of protoplast growth properties using quantitative single-cell tracking analysis
title_fullStr Determination of protoplast growth properties using quantitative single-cell tracking analysis
title_full_unstemmed Determination of protoplast growth properties using quantitative single-cell tracking analysis
title_short Determination of protoplast growth properties using quantitative single-cell tracking analysis
title_sort determination of protoplast growth properties using quantitative single-cell tracking analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118701/
https://www.ncbi.nlm.nih.gov/pubmed/35585602
http://dx.doi.org/10.1186/s13007-022-00895-x
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