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The individual-cell-based cryo-chip for the cryopreservation, manipulation and observation of spatially identifiable cells. II: Functional activity of cryopreserved cells
BACKGROUND: The cryopreservation and thawing processes are known to induce many deleterious effects in cells and might be detrimental to several cell types. There is an inherent variability in cellular responses among cell types and within individual cells of a given population with regard to their...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987892/ https://www.ncbi.nlm.nih.gov/pubmed/20973993 http://dx.doi.org/10.1186/1471-2121-11-83 |
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author | Afrimzon, Elena Zurgil, Naomi Shafran, Yana Ehrhart, Friederike Namer, Yaniv Moshkov, Sergei Sobolev, Maria Deutsch, Assaf Howitz, Steffen Greuner, Martin Thaele, Michael Meiser, Ina Zimmermann, Heiko Deutsch, Mordechai |
author_facet | Afrimzon, Elena Zurgil, Naomi Shafran, Yana Ehrhart, Friederike Namer, Yaniv Moshkov, Sergei Sobolev, Maria Deutsch, Assaf Howitz, Steffen Greuner, Martin Thaele, Michael Meiser, Ina Zimmermann, Heiko Deutsch, Mordechai |
author_sort | Afrimzon, Elena |
collection | PubMed |
description | BACKGROUND: The cryopreservation and thawing processes are known to induce many deleterious effects in cells and might be detrimental to several cell types. There is an inherent variability in cellular responses among cell types and within individual cells of a given population with regard to their ability to endure the freezing and thawing process. The aim of this study was to evaluate the fate of cryopreserved cells within an optical cryo apparatus, the individual-cell-based cryo-chip (i3C), by monitoring several basic cellular functional activities at the resolution of individual cells. RESULTS: In the present study, U937 cells underwent the freezing and thawing cycle in the i3C device. Then a panel of vital tests was performed, including the number of dead cells (PI staining), apoptotic rate (Annexin V staining), mitochondrial membrane potential (TMRM staining), cytoplasm membrane integrity and intracellular metabolism (FDA staining), as well as post-thawing cell proliferation assays. Cells that underwent the freezing - thawing cycle in i3C devices exhibited the same functional activity as control cells. Moreover, the combination of the multi-parametric analysis at a single cell resolution and the optical and biological features of the device enable an accurate determination of the functional status of individual cells and subsequent retrieval and utilization of the most valuable cells. CONCLUSIONS: The means and methodologies described here enable the freezing and thawing of spatially identifiable cells, as well as the efficient detection of viable, specific, highly biologically active cells for future applications. |
format | Text |
id | pubmed-2987892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29878922010-11-19 The individual-cell-based cryo-chip for the cryopreservation, manipulation and observation of spatially identifiable cells. II: Functional activity of cryopreserved cells Afrimzon, Elena Zurgil, Naomi Shafran, Yana Ehrhart, Friederike Namer, Yaniv Moshkov, Sergei Sobolev, Maria Deutsch, Assaf Howitz, Steffen Greuner, Martin Thaele, Michael Meiser, Ina Zimmermann, Heiko Deutsch, Mordechai BMC Cell Biol Methodology Article BACKGROUND: The cryopreservation and thawing processes are known to induce many deleterious effects in cells and might be detrimental to several cell types. There is an inherent variability in cellular responses among cell types and within individual cells of a given population with regard to their ability to endure the freezing and thawing process. The aim of this study was to evaluate the fate of cryopreserved cells within an optical cryo apparatus, the individual-cell-based cryo-chip (i3C), by monitoring several basic cellular functional activities at the resolution of individual cells. RESULTS: In the present study, U937 cells underwent the freezing and thawing cycle in the i3C device. Then a panel of vital tests was performed, including the number of dead cells (PI staining), apoptotic rate (Annexin V staining), mitochondrial membrane potential (TMRM staining), cytoplasm membrane integrity and intracellular metabolism (FDA staining), as well as post-thawing cell proliferation assays. Cells that underwent the freezing - thawing cycle in i3C devices exhibited the same functional activity as control cells. Moreover, the combination of the multi-parametric analysis at a single cell resolution and the optical and biological features of the device enable an accurate determination of the functional status of individual cells and subsequent retrieval and utilization of the most valuable cells. CONCLUSIONS: The means and methodologies described here enable the freezing and thawing of spatially identifiable cells, as well as the efficient detection of viable, specific, highly biologically active cells for future applications. BioMed Central 2010-10-25 /pmc/articles/PMC2987892/ /pubmed/20973993 http://dx.doi.org/10.1186/1471-2121-11-83 Text en Copyright ©2010 Afrimzon et al; 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 | Methodology Article Afrimzon, Elena Zurgil, Naomi Shafran, Yana Ehrhart, Friederike Namer, Yaniv Moshkov, Sergei Sobolev, Maria Deutsch, Assaf Howitz, Steffen Greuner, Martin Thaele, Michael Meiser, Ina Zimmermann, Heiko Deutsch, Mordechai The individual-cell-based cryo-chip for the cryopreservation, manipulation and observation of spatially identifiable cells. II: Functional activity of cryopreserved cells |
title | The individual-cell-based cryo-chip for the cryopreservation, manipulation and observation of spatially identifiable cells. II: Functional activity of cryopreserved cells |
title_full | The individual-cell-based cryo-chip for the cryopreservation, manipulation and observation of spatially identifiable cells. II: Functional activity of cryopreserved cells |
title_fullStr | The individual-cell-based cryo-chip for the cryopreservation, manipulation and observation of spatially identifiable cells. II: Functional activity of cryopreserved cells |
title_full_unstemmed | The individual-cell-based cryo-chip for the cryopreservation, manipulation and observation of spatially identifiable cells. II: Functional activity of cryopreserved cells |
title_short | The individual-cell-based cryo-chip for the cryopreservation, manipulation and observation of spatially identifiable cells. II: Functional activity of cryopreserved cells |
title_sort | individual-cell-based cryo-chip for the cryopreservation, manipulation and observation of spatially identifiable cells. ii: functional activity of cryopreserved cells |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987892/ https://www.ncbi.nlm.nih.gov/pubmed/20973993 http://dx.doi.org/10.1186/1471-2121-11-83 |
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