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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...

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Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
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.
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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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