Literature DB >> 2924590

Roles of unfrozen fraction, salt concentration, and changes in cell volume in the survival of frozen human erythrocytes.

P Mazur1, K W Cole.   

Abstract

The cause of slow freezing injury and the basis of the protection by solutes like glycerol are subjects of debate. During slow freezing, cells are sequestered in unfrozen channels between ice crystals that grow by removing pure water from the channels. As a consequence, the solute concentration in the channels rises and the volume of liquid in the channels progressively decreases. The rise in solute concentration, in turn, causes the cells to progressively shrink osmotically. Until recently cryobiologists have ascribed slow freezing injury to either the rise in solute (electrolyte) concentrations in the channels or to the consequent cell shrinkage, rather than to the decrease in the of the channels. Although ordinarily reciprocally coupled, it is possible to separate the composition of the channels from their size, or more precisely from the magnitude of the unfrozen fraction, by suspending cells in NaCl/cryoprotectant solutions in which the mole ratio of the two is held constant, but the molality of the NaCl is allowed to vary below and above isotonic. When human red cells are frozen in such solutions to temperatures that produce given NaCl concentrations (ms), but varying unfrozen fractions (U), survival at low U is found to be strongly dependent on U but independent of ms. At higher values of U, survival becomes inversely dependent on both ms and U. Although cell volume during freezing is independent of the NaCl tonicity in the solution, the cells in the several solutions differ in volume both prior to the onset of freezing and after the completion of thawing. We have now examined and compared the effect of returning the thawed cells to isotonic solutions and isotonic volume or nearly so, and find that there is little change in survival after exposure to low U, but that survival after exposure to high U values exhibits substantially increased sensitivity to ms, a sensitivity that is probably a manifestation of posthypertonic hemolysis. Low values of U were in general attained by the use of solutions with low tonicities of NaCl, and as a consequence cells frozen to low U values had larger volumes prior to freezing than cells frozen to higher U values. The significance of this confounding is discussed.

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Year:  1989        PMID: 2924590     DOI: 10.1016/0011-2240(89)90030-8

Source DB:  PubMed          Journal:  Cryobiology        ISSN: 0011-2240            Impact factor:   2.487


  12 in total

1.  Effects of cryopreservation on the transcriptome of human embryonic stem cells after thawing and culturing.

Authors:  Vilas Wagh; Kesavan Meganathan; Smita Jagtap; John Antonydas Gaspar; Johannes Winkler; Dimitry Spitkovsky; Jürgen Hescheler; Agapios Sachinidis
Journal:  Stem Cell Rev Rep       Date:  2011-09       Impact factor: 5.739

2.  Effects of freezing on membranes and proteins in LNCaP prostate tumor cells.

Authors:  Willem F Wolkers; Saravana K Balasubramanian; Emily L Ongstad; Helena C Zec; John C Bischof
Journal:  Biochim Biophys Acta       Date:  2006-12-13

3.  Protein kinase A inhibitor, H89, significantly enhances survival rate of dissociated human embryonic stem cells following cryopreservation.

Authors:  Liang Zhang; Yanqing Xu; Jiandong Xu; Yuping Wei; Xia Xu
Journal:  Cell Prolif       Date:  2016-08-03       Impact factor: 6.831

4.  The temperature of intracellular ice formation in mouse oocytes vs. the unfrozen fraction at that temperature.

Authors:  Peter Mazur; Irina L Pinn; F W Kleinhans
Journal:  Cryobiology       Date:  2007-02-14       Impact factor: 2.487

5.  High post-thaw survival of ram sperm after partial freeze-drying.

Authors:  Amir Arav; Antonella Idda; Stefano Mario Nieddu; Yehudit Natan; Sergio Ledda
Journal:  J Assist Reprod Genet       Date:  2018-03-14       Impact factor: 3.412

6.  Implications of variability in cell membrane permeability for design of methods to remove glycerol from frozen-thawed erythrocytes.

Authors:  John M Lahmann; Cynthia Cruz Sanchez; James D Benson; Jason P Acker; Adam Z Higgins
Journal:  Cryobiology       Date:  2020-01-11       Impact factor: 2.487

7.  Stability of phosphatidylethanol species in spiked and authentic whole blood and matching dried blood spots.

Authors:  Andrea Faller; Barbara Richter; Matthias Kluge; Patrick Koenig; H K Seitz; Gisela Skopp
Journal:  Int J Legal Med       Date:  2012-12-04       Impact factor: 2.686

Review 8.  Engineering complex tissues.

Authors:  Antonios G Mikos; Susan W Herring; Pannee Ochareon; Jennifer Elisseeff; Helen H Lu; Rita Kandel; Frederick J Schoen; Mehmet Toner; David Mooney; Anthony Atala; Mark E Van Dyke; David Kaplan; Gordana Vunjak-Novakovic
Journal:  Tissue Eng       Date:  2006-12

9.  Interactions among pre-cooling, cryoprotectant, cooling, and thawing for sperm cryopreservation in rhesus monkeys.

Authors:  Qiaoxiang Dong; Dana Hill; Catherine A VandeVoort
Journal:  Cryobiology       Date:  2009-08-15       Impact factor: 2.487

10.  Sperm cell population dynamics in ram semen during the cryopreservation process.

Authors:  Manuel Ramón; M Dolores Pérez-Guzmán; Pilar Jiménez-Rabadán; Milagros C Esteso; Olga García-Álvarez; Alejandro Maroto-Morales; Luis Anel-López; Ana J Soler; M Rocío Fernández-Santos; J Julián Garde
Journal:  PLoS One       Date:  2013-03-27       Impact factor: 3.240

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