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A simple way to identify non-viable cells within living plant tissue using confocal microscopy

BACKGROUND: Plant cell death is a normal process during plant development. Mutant plants may exhibit misregulation of this process, which can lead to severe growth defects. Simple ways of visualising cell death in living plant tissues can aid the study of plant development and physiology. RESULTS: S...

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Detalles Bibliográficos
Autores principales: Truernit, Elisabeth, Haseloff, Jim
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442066/
https://www.ncbi.nlm.nih.gov/pubmed/18573203
http://dx.doi.org/10.1186/1746-4811-4-15
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author Truernit, Elisabeth
Haseloff, Jim
author_facet Truernit, Elisabeth
Haseloff, Jim
author_sort Truernit, Elisabeth
collection PubMed
description BACKGROUND: Plant cell death is a normal process during plant development. Mutant plants may exhibit misregulation of this process, which can lead to severe growth defects. Simple ways of visualising cell death in living plant tissues can aid the study of plant development and physiology. RESULTS: Spectral variants of the fluorescent SYTOX dyes were tested for their usefulness for the detection of non-viable cells within plant embryos and roots using confocal laser-scanning microscopy. The dyes were selective for non-viable cells and showed very little background staining in living cells. Simultaneous detection of SYTOX dye and fluorescent protein (e.g. GFP) fluorescence was possible. CONCLUSION: The fluorescent SYTOX dyes are useful for an easy and quick first assay of plant cell viability in living plant samples using fluorescence and confocal laser-scanning microscopy.
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spelling pubmed-24420662008-07-01 A simple way to identify non-viable cells within living plant tissue using confocal microscopy Truernit, Elisabeth Haseloff, Jim Plant Methods Research BACKGROUND: Plant cell death is a normal process during plant development. Mutant plants may exhibit misregulation of this process, which can lead to severe growth defects. Simple ways of visualising cell death in living plant tissues can aid the study of plant development and physiology. RESULTS: Spectral variants of the fluorescent SYTOX dyes were tested for their usefulness for the detection of non-viable cells within plant embryos and roots using confocal laser-scanning microscopy. The dyes were selective for non-viable cells and showed very little background staining in living cells. Simultaneous detection of SYTOX dye and fluorescent protein (e.g. GFP) fluorescence was possible. CONCLUSION: The fluorescent SYTOX dyes are useful for an easy and quick first assay of plant cell viability in living plant samples using fluorescence and confocal laser-scanning microscopy. BioMed Central 2008-06-23 /pmc/articles/PMC2442066/ /pubmed/18573203 http://dx.doi.org/10.1186/1746-4811-4-15 Text en Copyright © 2008 Truernit and Haseloff; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Truernit, Elisabeth
Haseloff, Jim
A simple way to identify non-viable cells within living plant tissue using confocal microscopy
title A simple way to identify non-viable cells within living plant tissue using confocal microscopy
title_full A simple way to identify non-viable cells within living plant tissue using confocal microscopy
title_fullStr A simple way to identify non-viable cells within living plant tissue using confocal microscopy
title_full_unstemmed A simple way to identify non-viable cells within living plant tissue using confocal microscopy
title_short A simple way to identify non-viable cells within living plant tissue using confocal microscopy
title_sort simple way to identify non-viable cells within living plant tissue using confocal microscopy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442066/
https://www.ncbi.nlm.nih.gov/pubmed/18573203
http://dx.doi.org/10.1186/1746-4811-4-15
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