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Label-free optical interferometric microscopy to characterize morphodynamics in living plants
During the last century, fluorescence microscopy has played a pivotal role in a range of scientific discoveries. The success of fluorescence microscopy has prevailed despite several shortcomings like measurement time, photobleaching, temporal resolution, and specific sample preparation. To bypass th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10239806/ https://www.ncbi.nlm.nih.gov/pubmed/37284726 http://dx.doi.org/10.3389/fpls.2023.1156478 |
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author | Ebrahimi, Samira Moreno-Pescador, Guillermo Persson, Staffan Jauffred, Liselotte Bendix, Poul Martin |
author_facet | Ebrahimi, Samira Moreno-Pescador, Guillermo Persson, Staffan Jauffred, Liselotte Bendix, Poul Martin |
author_sort | Ebrahimi, Samira |
collection | PubMed |
description | During the last century, fluorescence microscopy has played a pivotal role in a range of scientific discoveries. The success of fluorescence microscopy has prevailed despite several shortcomings like measurement time, photobleaching, temporal resolution, and specific sample preparation. To bypass these obstacles, label-free interferometric methods have been developed. Interferometry exploits the full wavefront information of laser light after interaction with biological material to yield interference patterns that contain information about structure and activity. Here, we review recent studies in interferometric imaging of plant cells and tissues, using techniques such as biospeckle imaging, optical coherence tomography, and digital holography. These methods enable quantification of cell morphology and dynamic intracellular measurements over extended periods of time. Recent investigations have showcased the potential of interferometric techniques for precise identification of seed viability and germination, plant diseases, plant growth and cell texture, intracellular activity and cytoplasmic transport. We envision that further developments of these label-free approaches, will allow for high-resolution, dynamic imaging of plants and their organelles, ranging in scales from sub-cellular to tissue and from milliseconds to hours. |
format | Online Article Text |
id | pubmed-10239806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102398062023-06-06 Label-free optical interferometric microscopy to characterize morphodynamics in living plants Ebrahimi, Samira Moreno-Pescador, Guillermo Persson, Staffan Jauffred, Liselotte Bendix, Poul Martin Front Plant Sci Plant Science During the last century, fluorescence microscopy has played a pivotal role in a range of scientific discoveries. The success of fluorescence microscopy has prevailed despite several shortcomings like measurement time, photobleaching, temporal resolution, and specific sample preparation. To bypass these obstacles, label-free interferometric methods have been developed. Interferometry exploits the full wavefront information of laser light after interaction with biological material to yield interference patterns that contain information about structure and activity. Here, we review recent studies in interferometric imaging of plant cells and tissues, using techniques such as biospeckle imaging, optical coherence tomography, and digital holography. These methods enable quantification of cell morphology and dynamic intracellular measurements over extended periods of time. Recent investigations have showcased the potential of interferometric techniques for precise identification of seed viability and germination, plant diseases, plant growth and cell texture, intracellular activity and cytoplasmic transport. We envision that further developments of these label-free approaches, will allow for high-resolution, dynamic imaging of plants and their organelles, ranging in scales from sub-cellular to tissue and from milliseconds to hours. Frontiers Media S.A. 2023-05-22 /pmc/articles/PMC10239806/ /pubmed/37284726 http://dx.doi.org/10.3389/fpls.2023.1156478 Text en Copyright © 2023 Ebrahimi, Moreno-Pescador, Persson, Jauffred and Bendix https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Ebrahimi, Samira Moreno-Pescador, Guillermo Persson, Staffan Jauffred, Liselotte Bendix, Poul Martin Label-free optical interferometric microscopy to characterize morphodynamics in living plants |
title | Label-free optical interferometric microscopy to characterize morphodynamics in living plants |
title_full | Label-free optical interferometric microscopy to characterize morphodynamics in living plants |
title_fullStr | Label-free optical interferometric microscopy to characterize morphodynamics in living plants |
title_full_unstemmed | Label-free optical interferometric microscopy to characterize morphodynamics in living plants |
title_short | Label-free optical interferometric microscopy to characterize morphodynamics in living plants |
title_sort | label-free optical interferometric microscopy to characterize morphodynamics in living plants |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10239806/ https://www.ncbi.nlm.nih.gov/pubmed/37284726 http://dx.doi.org/10.3389/fpls.2023.1156478 |
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