Literature DB >> 15975568

Extra- and intracellular ice formation in mouse oocytes.

Peter Mazur1, Shinsuke Seki, Irina L Pinn, F W Kleinhans, Keisuke Edashige.   

Abstract

The occurrence of intracellular ice formation (IIF) during freezing, or the lack there of, is the single most important factor determining whether or not cells survive cryopreservation. One important determinant of IIF is the temperature at which a supercooled cell nucleates. To avoid intracellular ice formation, the cell must be cooled slowly enough so that osmotic dehydration eliminates nearly all cell supercooling before reaching that temperature. This report is concerned with factors that determine the nucleation temperature in mouse oocytes. Chief among these is the concentration of cryoprotective additive (here, glycerol or ethylene glycol). The temperature for IIF decreases from -14 degrees C in buffered isotonic saline (PBS) to -41 degrees C in 1M glycerol/PBS and 1.5M ethylene glycol/PBS. The latter rapidly permeates the oocyte; the former does not. The initial extracellular freezing at -3.9 to -7.8 degrees C, depending on the CPA concentration, deforms the cell. In PBS that deformation often leads to IIF; in CPA it does not. The oocytes are surrounded by a zona pellucida. That structure appears to impede the growth of external ice through it, but not to block it. In most cases, IIF is characterized by an abrupt blackening or flashing during cooling. But in some cases, especially with dezonated oocytes, a pale brown veil abruptly forms during cooling followed by slower blackening during warming. Above -30 degrees C, flashing occurs in a fraction of a second. Below -30 degrees C, it commonly occurs much more slowly. We have observed instances where flashing is accompanied by the abrupt ejection of cytoplasm. During freezing, cells lie in unfrozen channels between the growing external ice. From phase diagram data, we have computed the fraction of water and solution that remains unfrozen at the observed flash temperatures and the concentrations of salt and CPA in those channels. The results are somewhat ambiguous as to which of these characteristics best correlates with IIF.

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Year:  2005        PMID: 15975568     DOI: 10.1016/j.cryobiol.2005.04.008

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


  27 in total

1.  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

2.  Zebrafish embryos (Danio rerio) using microinjection.

Authors:  Julia Kopeika; Tiantian Zhang; David Rawson
Journal:  Cryo Letters       Date:  2006 Sep-Oct       Impact factor: 1.066

3.  Kinetics and activation energy of recrystallization of intracellular ice in mouse oocytes subjected to interrupted rapid cooling.

Authors:  Shinsuke Seki; Peter Mazur
Journal:  Cryobiology       Date:  2008-02-12       Impact factor: 2.487

4.  The temperature and type of intracellular ice formation in preimplantation mouse embryos as a function of the developmental stage.

Authors:  Shinsuke Seki; Peter Mazur
Journal:  Biol Reprod       Date:  2010-02-17       Impact factor: 4.285

5.  Effect of warming rate on the survival of vitrified mouse oocytes and on the recrystallization of intracellular ice.

Authors:  Shinsuke Seki; Peter Mazur
Journal:  Biol Reprod       Date:  2008-06-18       Impact factor: 4.285

6.  Effect of the expression of aquaporins 1 and 3 in mouse oocytes and compacted eight-cell embryos on the nucleation temperature for intracellular ice formation.

Authors:  Shinsuke Seki; Keisuke Edashige; Sakiko Wada; Peter Mazur
Journal:  Reproduction       Date:  2011-07-06       Impact factor: 3.906

7.  Bacterial Ice Nucleation in Monodisperse D2O and H2O-in-Oil Emulsions.

Authors:  Lindong Weng; Shannon N Tessier; Kyle Smith; Jon F Edd; Shannon L Stott; Mehmet Toner
Journal:  Langmuir       Date:  2016-08-18       Impact factor: 3.882

8.  Survival of mouse oocytes after being cooled in a vitrification solution to -196°C at 95° to 70,000°C/min and warmed at 610° to 118,000°C/min: A new paradigm for cryopreservation by vitrification.

Authors:  Peter Mazur; Shinsuke Seki
Journal:  Cryobiology       Date:  2010-11-03       Impact factor: 2.487

9.  Comparison between the temperatures of intracellular ice formation in fresh mouse oocytes and embryos and those previously subjected to a vitrification procedure.

Authors:  Shinsuke Seki; Peter Mazur
Journal:  Cryobiology       Date:  2010-03-31       Impact factor: 2.487

Review 10.  A biologist's view of the relevance of thermodynamics and physical chemistry to cryobiology.

Authors:  Peter Mazur
Journal:  Cryobiology       Date:  2009-12-04       Impact factor: 2.487

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