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Whole-Cell Multiparameter Assay for Ricin and Abrin Activity-Based Digital Holographic Microscopy
Ricin and abrin are ribosome-inactivating proteins leading to inhibition of protein synthesis and cell death. These toxins are considered some of the most potent and lethal toxins against which there is no available antidote. Digital holographic microscopy (DHM) is a time-lapse, label-free, and noni...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468687/ https://www.ncbi.nlm.nih.gov/pubmed/30909438 http://dx.doi.org/10.3390/toxins11030174 |
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author | Makdasi, Efi Laskar, Orly Milrot, Elad Schuster, Ofir Shmaya, Shlomo Yitzhaki, Shmuel |
author_facet | Makdasi, Efi Laskar, Orly Milrot, Elad Schuster, Ofir Shmaya, Shlomo Yitzhaki, Shmuel |
author_sort | Makdasi, Efi |
collection | PubMed |
description | Ricin and abrin are ribosome-inactivating proteins leading to inhibition of protein synthesis and cell death. These toxins are considered some of the most potent and lethal toxins against which there is no available antidote. Digital holographic microscopy (DHM) is a time-lapse, label-free, and noninvasive imaging technique that can provide phase information on morphological features of cells. In this study, we employed DHM to evaluate the morphological changes of cell lines during ricin and abrin intoxication. We showed that the effect of these toxins is characterized by a decrease in cell confluence and changes in morphological parameters such as cell area, perimeter, irregularity, and roughness. In addition, changes in optical parameters such as phase-shift, optical thickness, and effective-calculated volume were observed. These effects were completely inhibited by specific neutralizing antibodies. An enhanced intoxication effect was observed for preadherent compared to adherent cells, as was detected in early morphology changes and confirmed by annexin V/propidium iodide (PI) apoptosis assay. Detection of the dynamic changes in cell morphology at initial stages of cell intoxication by DHM emphasizes the highly sensitive and rapid nature of this method, allowing the early detection of active toxins. |
format | Online Article Text |
id | pubmed-6468687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64686872019-04-22 Whole-Cell Multiparameter Assay for Ricin and Abrin Activity-Based Digital Holographic Microscopy Makdasi, Efi Laskar, Orly Milrot, Elad Schuster, Ofir Shmaya, Shlomo Yitzhaki, Shmuel Toxins (Basel) Article Ricin and abrin are ribosome-inactivating proteins leading to inhibition of protein synthesis and cell death. These toxins are considered some of the most potent and lethal toxins against which there is no available antidote. Digital holographic microscopy (DHM) is a time-lapse, label-free, and noninvasive imaging technique that can provide phase information on morphological features of cells. In this study, we employed DHM to evaluate the morphological changes of cell lines during ricin and abrin intoxication. We showed that the effect of these toxins is characterized by a decrease in cell confluence and changes in morphological parameters such as cell area, perimeter, irregularity, and roughness. In addition, changes in optical parameters such as phase-shift, optical thickness, and effective-calculated volume were observed. These effects were completely inhibited by specific neutralizing antibodies. An enhanced intoxication effect was observed for preadherent compared to adherent cells, as was detected in early morphology changes and confirmed by annexin V/propidium iodide (PI) apoptosis assay. Detection of the dynamic changes in cell morphology at initial stages of cell intoxication by DHM emphasizes the highly sensitive and rapid nature of this method, allowing the early detection of active toxins. MDPI 2019-03-22 /pmc/articles/PMC6468687/ /pubmed/30909438 http://dx.doi.org/10.3390/toxins11030174 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Makdasi, Efi Laskar, Orly Milrot, Elad Schuster, Ofir Shmaya, Shlomo Yitzhaki, Shmuel Whole-Cell Multiparameter Assay for Ricin and Abrin Activity-Based Digital Holographic Microscopy |
title | Whole-Cell Multiparameter Assay for Ricin and Abrin Activity-Based Digital Holographic Microscopy |
title_full | Whole-Cell Multiparameter Assay for Ricin and Abrin Activity-Based Digital Holographic Microscopy |
title_fullStr | Whole-Cell Multiparameter Assay for Ricin and Abrin Activity-Based Digital Holographic Microscopy |
title_full_unstemmed | Whole-Cell Multiparameter Assay for Ricin and Abrin Activity-Based Digital Holographic Microscopy |
title_short | Whole-Cell Multiparameter Assay for Ricin and Abrin Activity-Based Digital Holographic Microscopy |
title_sort | whole-cell multiparameter assay for ricin and abrin activity-based digital holographic microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468687/ https://www.ncbi.nlm.nih.gov/pubmed/30909438 http://dx.doi.org/10.3390/toxins11030174 |
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