Optimization of cryoprotectant addition and removal procedures for vitrification of adherent mammalian cells

Cryopreservation of adherent cells may be advantageous for cell types that are difficult to preserve in suspension or when it is necessary to preserve characteristics of the adherent cultured cells. Vitrification is a promising procedure for the preservation of adherent cells that prevents ice cryst...

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Main Author: Fry Davidson, Allyson
Other Authors: Higgins, Adam
Language:en_US
Published: 2013
Subjects:
Online Access:http://hdl.handle.net/1957/36912
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spelling ndltd-ORGSU-oai-ir.library.oregonstate.edu-1957-369122013-02-16T03:30:43ZOptimization of cryoprotectant addition and removal procedures for vitrification of adherent mammalian cellsFry Davidson, Allysonvitrificationcryopreservationadherentmembrane permeabilityrational designCells -- CryopreservationCell adhesionEndothelial cells -- CryopreservationNeurons -- CryopreservationCells -- PermeabilityCryopreservation of adherent cells may be advantageous for cell types that are difficult to preserve in suspension or when it is necessary to preserve characteristics of the adherent cultured cells. Vitrification is a promising procedure for the preservation of adherent cells that prevents ice crystal formation and the resulting dissociation and morphological damage. To successfully vitrify adherent cells, high concentrations of CPA are required which increases the likelihood of osmotic and toxic damage. In this dissertation, we describe a rational design strategy that predicts mathematically optimized CPA addition and removal procedures based on the minimization of a toxicity cost function. These rationally designed procedures rely on the accurate knowledge of cell biophysical parameters. We validate an in situ calcein fluorescence quenching method for the determination of membrane permeability parameters for adherent cells. We also describe the determination of osmotic tolerance limits for adherent cells. We use rational design strategies to determine CPA addition and removal procedures for adherent endothelial cells, neuronal cells, and induced pluripotent stem cells as well as oocytes. Also, we provide experimental support for the feasibility of these methods using adherent endothelial cells. The mathematical methods and experimental procedures outlined in this dissertation are important tools for the design of addition and removal procedures for concentrated CPA solutions. This dissertation is an important step toward successful design and implementation of vitrification strategies for adherent cells and tissues.Graduation date: 2013Access restricted to the OSU Community at author's request from Feb. 14, 2013 - Feb. 14, 2015Higgins, Adam2013-02-15T18:41:02Z2013-01-302013-01-302015-02-14Thesis/Dissertationhttp://hdl.handle.net/1957/36912en_US
collection NDLTD
language en_US
sources NDLTD
topic vitrification
cryopreservation
adherent
membrane permeability
rational design
Cells -- Cryopreservation
Cell adhesion
Endothelial cells -- Cryopreservation
Neurons -- Cryopreservation
Cells -- Permeability
spellingShingle vitrification
cryopreservation
adherent
membrane permeability
rational design
Cells -- Cryopreservation
Cell adhesion
Endothelial cells -- Cryopreservation
Neurons -- Cryopreservation
Cells -- Permeability
Fry Davidson, Allyson
Optimization of cryoprotectant addition and removal procedures for vitrification of adherent mammalian cells
description Cryopreservation of adherent cells may be advantageous for cell types that are difficult to preserve in suspension or when it is necessary to preserve characteristics of the adherent cultured cells. Vitrification is a promising procedure for the preservation of adherent cells that prevents ice crystal formation and the resulting dissociation and morphological damage. To successfully vitrify adherent cells, high concentrations of CPA are required which increases the likelihood of osmotic and toxic damage. In this dissertation, we describe a rational design strategy that predicts mathematically optimized CPA addition and removal procedures based on the minimization of a toxicity cost function. These rationally designed procedures rely on the accurate knowledge of cell biophysical parameters. We validate an in situ calcein fluorescence quenching method for the determination of membrane permeability parameters for adherent cells. We also describe the determination of osmotic tolerance limits for adherent cells. We use rational design strategies to determine CPA addition and removal procedures for adherent endothelial cells, neuronal cells, and induced pluripotent stem cells as well as oocytes. Also, we provide experimental support for the feasibility of these methods using adherent endothelial cells. The mathematical methods and experimental procedures outlined in this dissertation are important tools for the design of addition and removal procedures for concentrated CPA solutions. This dissertation is an important step toward successful design and implementation of vitrification strategies for adherent cells and tissues. === Graduation date: 2013 === Access restricted to the OSU Community at author's request from Feb. 14, 2013 - Feb. 14, 2015
author2 Higgins, Adam
author_facet Higgins, Adam
Fry Davidson, Allyson
author Fry Davidson, Allyson
author_sort Fry Davidson, Allyson
title Optimization of cryoprotectant addition and removal procedures for vitrification of adherent mammalian cells
title_short Optimization of cryoprotectant addition and removal procedures for vitrification of adherent mammalian cells
title_full Optimization of cryoprotectant addition and removal procedures for vitrification of adherent mammalian cells
title_fullStr Optimization of cryoprotectant addition and removal procedures for vitrification of adherent mammalian cells
title_full_unstemmed Optimization of cryoprotectant addition and removal procedures for vitrification of adherent mammalian cells
title_sort optimization of cryoprotectant addition and removal procedures for vitrification of adherent mammalian cells
publishDate 2013
url http://hdl.handle.net/1957/36912
work_keys_str_mv AT frydavidsonallyson optimizationofcryoprotectantadditionandremovalproceduresforvitrificationofadherentmammaliancells
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