Cryopreservation of Equine and Bovine Erythrocytes Using Combined Protective Media

Authors

  • Pavlo Yu. Ulizko Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv
  • Olena M Bobrova Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv
  • Oleg A Nardid 1. Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv 2. V.N. Karazin Kharkiv National University, Kharkiv
  • Pavlo Ðœ. Zubov Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv
  • Igor F. Kovalenko Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv
  • Vadim M. Kuchkov V.N. Karazin Kharkiv National University, Kharkiv
  • Larisa A. Vodopyanova Kharkiv State Zooveterinary Academy, Kharkiv

DOI:

https://doi.org/10.15407/cryo29.03.255

Keywords:

cryopreservation, equine and bovine red blood cells, combined cryopreservation medium, hemolysis, fluorescent dye

Abstract

A comparative analysis of the effectiveness of equine and bovine erythrocytes’ cryopreservation with the use of one component (20% DMSO) and combined (10% DMSO, 20% PEO-1500) protective medium was carried out. Using fluorescence microscopy and flow cytometry, it has been shown that the 3-DAB fluorescent dye paints the membranes of red blood cells and can be used to evaluate their condition at all cryopreservation stages. It was found that the use of combined protective medium can significantly improve the results of cryopreservation of equine and bovine red blood cells in comparison with one-component media. By cytometric data it has been defined that the parameters of equine erythrocytes after preservation in DMSO-based medium did not correspond the control even after cryoprotectant washing, but after freezing in combined cryoprotective medium and cryoprotectant washing they matched the control. The fluorescence intensification of equine and bovine erythrocytes on fluorescence images and changes in cytograms after mixing cells with 20% DMSO suggests its strong membranotropic influence. Hemolysis level with applying a combined cryoprotective medium of equine and bovine erythrocytes is significantly lower than with the application of 20% DMSO after all cryopreservation stages.

 

Probl Cryobiol Cryomed 2019; 29(3): 255–265.

Author Biographies

Pavlo Yu. Ulizko, Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv

Department of Cryobiophysics

Olena M Bobrova, Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv

Department of Cryobiophysics

Oleg A Nardid, 1. Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv 2. V.N. Karazin Kharkiv National University, Kharkiv

Department of Cryobiophysics

Pavlo М. Zubov, Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv

Department of Cryocytology

Igor F. Kovalenko, Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Kharkiv

Department for Low Temperature Preservation

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Published

2019-09-19

How to Cite

Ulizko, P. Y., Bobrova, O. M., Nardid, O. A., Zubov, P. Ðœ., Kovalenko, I. F., Kuchkov, V. M., & Vodopyanova, L. A. (2019). Cryopreservation of Equine and Bovine Erythrocytes Using Combined Protective Media. Problems of Cryobiology and Cryomedicine, 29(3), 255–265. https://doi.org/10.15407/cryo29.03.255

Issue

Section

Cryopreservation of Biological Resources