Cargando…
An optical imaging chamber for viewing living plant cells and tissues at high resolution for extended periods
BACKGROUND: Recent developments in both microscopy and fluorescent protein technologies have made live imaging a powerful tool for the study of plant cells. However, the complications of keeping plant material alive during a long duration experiment while maintaining maximum resolution has limited t...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371620/ https://www.ncbi.nlm.nih.gov/pubmed/25806083 http://dx.doi.org/10.1186/s13007-015-0065-7 |
_version_ | 1782363066798702592 |
---|---|
author | Calder, Grant Hindle, Chris Chan, Jordi Shaw, Peter |
author_facet | Calder, Grant Hindle, Chris Chan, Jordi Shaw, Peter |
author_sort | Calder, Grant |
collection | PubMed |
description | BACKGROUND: Recent developments in both microscopy and fluorescent protein technologies have made live imaging a powerful tool for the study of plant cells. However, the complications of keeping plant material alive during a long duration experiment while maintaining maximum resolution has limited the use of these methods. RESULTS: Here, we describe an imaging chamber designed to overcome these limitations, which is flexible enough to support a range of sizes of plant materials. We were able use confocal microscopy to follow growth and development of plant cells and tissues over several days. The chamber design is based on a perfusion system, so that the addition of drugs and other experimental treatments are also possible. CONCLUSIONS: In this article we present a design of imaging chamber that makes it possible to image plant material with high resolution for extended periods of time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13007-015-0065-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4371620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43716202015-03-25 An optical imaging chamber for viewing living plant cells and tissues at high resolution for extended periods Calder, Grant Hindle, Chris Chan, Jordi Shaw, Peter Plant Methods Methodology BACKGROUND: Recent developments in both microscopy and fluorescent protein technologies have made live imaging a powerful tool for the study of plant cells. However, the complications of keeping plant material alive during a long duration experiment while maintaining maximum resolution has limited the use of these methods. RESULTS: Here, we describe an imaging chamber designed to overcome these limitations, which is flexible enough to support a range of sizes of plant materials. We were able use confocal microscopy to follow growth and development of plant cells and tissues over several days. The chamber design is based on a perfusion system, so that the addition of drugs and other experimental treatments are also possible. CONCLUSIONS: In this article we present a design of imaging chamber that makes it possible to image plant material with high resolution for extended periods of time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13007-015-0065-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-22 /pmc/articles/PMC4371620/ /pubmed/25806083 http://dx.doi.org/10.1186/s13007-015-0065-7 Text en © Calder et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Calder, Grant Hindle, Chris Chan, Jordi Shaw, Peter An optical imaging chamber for viewing living plant cells and tissues at high resolution for extended periods |
title | An optical imaging chamber for viewing living plant cells and tissues at high resolution for extended periods |
title_full | An optical imaging chamber for viewing living plant cells and tissues at high resolution for extended periods |
title_fullStr | An optical imaging chamber for viewing living plant cells and tissues at high resolution for extended periods |
title_full_unstemmed | An optical imaging chamber for viewing living plant cells and tissues at high resolution for extended periods |
title_short | An optical imaging chamber for viewing living plant cells and tissues at high resolution for extended periods |
title_sort | optical imaging chamber for viewing living plant cells and tissues at high resolution for extended periods |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371620/ https://www.ncbi.nlm.nih.gov/pubmed/25806083 http://dx.doi.org/10.1186/s13007-015-0065-7 |
work_keys_str_mv | AT caldergrant anopticalimagingchamberforviewinglivingplantcellsandtissuesathighresolutionforextendedperiods AT hindlechris anopticalimagingchamberforviewinglivingplantcellsandtissuesathighresolutionforextendedperiods AT chanjordi anopticalimagingchamberforviewinglivingplantcellsandtissuesathighresolutionforextendedperiods AT shawpeter anopticalimagingchamberforviewinglivingplantcellsandtissuesathighresolutionforextendedperiods AT caldergrant opticalimagingchamberforviewinglivingplantcellsandtissuesathighresolutionforextendedperiods AT hindlechris opticalimagingchamberforviewinglivingplantcellsandtissuesathighresolutionforextendedperiods AT chanjordi opticalimagingchamberforviewinglivingplantcellsandtissuesathighresolutionforextendedperiods AT shawpeter opticalimagingchamberforviewinglivingplantcellsandtissuesathighresolutionforextendedperiods |