THE NANOSTRUCTURE OF ERYTHROCYTE MEMBRANES UNDER BLOOD INTOXICATION: AN ATOMIC FORCE MICROSCOPY STUDY

Cover Page


Cite item

Full Text

Abstract

Background: The effects of toxins on nanostructure of blood cells are one of the key problems of biophysics and medicine. Erythrocyte morphology and membrane structure are recognized as the main parameters of blood quality. Therefore, analysis of membrane defects under toxin effects seems an urgent issue. Aim: To identify characteristic features and patterns of changes in membrane nanostructure under hemin intoxication and during extended storage of erythrocyte suspension. Materials and methods: The study was done in vitro in human whole blood with addition of hemin, аnd in erythrocyte suspension with a CPD blood preservative stored at 4 °С for 30 days. The nanostructure of erythrocyte membrane was assessed by atomic force microscopy. Results: Characteristic size of space periods between “granules” was from 120 to 200 nm. “Granule” numbers within a topological defect varied from 4 to 5 and to several dozens. Such domains arose virtually on all cells in erythrocyte suspension, as well as after hemin addition to the blood. An increase in hemin intoxication and an increase in a storage time were associated by increases in echinocyte numbers that subsequently transformed into spherical echinocytes. Both under hemin and during the storage of erythrocyte suspension for 9 to 12 days, a specific abnormality in nanostructure of erythrocyte membrane was observed: structural clusters, i.e., domains with granular structure, were formed. Conclusion: The experiments showed that both hemin and oxidative processes in the blood can specifically affect the nanostructure of erythrocyte membranes with formation of domains on their surface. The specific size of granular structures in the domains is from 100 to 200 nm that coincides with a  specific size of spectrin matrix. These results can be used in basic and applied medicine, in blood transfusion, for the analysis of a toxin effects in the human body. The biophysical mechanisms of domain formation can become a  basis for the study on a toxin – membrane cross-talk.

About the authors

V. A. Sergunova

V.A. Negovsky Scientific Research Institute of General Reanimatology; 25/2 Petrovka ul., Moscow, 107031, Russian Federation

Author for correspondence.
Email: orbf@mail.ru
PhD (in Biology), Senior Research Fellow, Laboratory of Biophysics of Cells Membranes in Critical States Россия

A. P. Chernyaev

Lomonosov Moscow State University; 1 Leninskie gory, Moscow, 119991, Russian Federation

Email: orbf@mail.ru
PhD (in Physics and Mathematics), Professor, Head of the Chair of Physics of Accelerators and Radiation Medicine, Faculty of Physics Россия

A. P. Kozlov

I.M. Sechenov First Moscow State Medical University; 8/2 Trubetskaya ul., Moscow, 119991, Russian Federation

Email: orbf@mail.ru
PhD (in Physics and Mathematics), Associate Professor, Chair of Medical and Biological Physics Россия

U. A. Bliznyuk

Lomonosov Moscow State University; 1 Leninskie gory, Moscow, 119991, Russian Federation

Email: orbf@mail.ru
PhD (in Physics and Mathematics), Senior Lecturer, Chair of Physics of Accelerators and Radiation Medicine, Faculty of Physics Россия

P. Yu. Borshchegovskaya

Lomonosov Moscow State University; 1 Leninskie gory, Moscow, 119991, Russian Federation

Email: orbf@mail.ru
PhD (in Physics and Mathematics), Lecturer, Chair of Physics of Accelerators and Radiation Medicine, Faculty of Physics Россия

E. K. Kozlova

V.A. Negovsky Scientific Research Institute of General Reanimatology; 25/2 Petrovka ul., Moscow, 107031, Russian Federation
Lomonosov Moscow State University; 1 Leninskie gory, Moscow, 119991, Russian Federation
I.M. Sechenov First Moscow State Medical University; 8/2 Trubetskaya ul., Moscow, 119991, Russian Federation

Email: orbf@mail.ru
PhD (in Physics and Mathematics), Leading Research Fellow, Laboratory of Biophysics of Cells Membranes in Critical States1 ; Professor, Chair of Physics of Accelerators and Radiation Medicine, Faculty of Physics2 ;Professor, Chair of Medical and Biological Physics3 Россия

A. M. Chernysh

V.A. Negovsky Scientific Research Institute of General Reanimatology; 25/2 Petrovka ul., Moscow, 107031, Russian Federation
I.M. Sechenov First Moscow State Medical University; 8/2 Trubetskaya ul., Moscow, 119991, Russian Federation

Email: orbf@mail.ru
PhD (in Biology), Head of Laboratory of Biophysics of Cells Membranes in Critical States1 ; Professor, Chair of Medical and Biological Physics Россия

References

  1. Girasole M, Pompeo G, Cricenti A, Longo G, Boumis G, Bellelli A, Amiconi S. The how, when, and why of the aging signals appearing on the human erythrocyte membrane: an atomic force microscopy study of surface roughness. Nanomedicine. 2010;6(6):760–8. doi: 10.1016/j. nano.2010.06.004.
  2. Umbreit J. Methemoglobin – it's not just blue: a concise review. Am J Hematol. 2007;82(2):134–44. doi: 10.1002/ajh.20738.
  3. Solar I, Muller-Eberhard U, Shviro Y, Shaklai N. Long-term intercalation of residual hemin in erythrocyte membranes distorts the cell. Biochim Biophys Acta. 1991;1062(1):51–8.
  4. Kozlova Е, Chernysh А, Moroz V, Sergunova V, Gudkova О, Kuzovlev А. Nanodefects of membranes cause destruction of packed red blood cells during long-term storage. Exp Cell Res. 2015;337(2):192–201. doi: 10.1016/0005- 2736(91)90334-5.
  5. Костин АИ, Майорова ОА, Ложкин АВ, Почтарь МЕ, Демичева МИ, Кузмичев ВА, Луговская СА, Наумова ЕВ, Кисиличина ДГ, Андрейцева ЭВ, Долгов ВВ. К вопросу о контроле качества эритроцитсодержащих компонентов крови, обедненных лейкоцитами. Трансфузиология. 2011;12(2):12–33.
  6. Berezina TL, Zaets SB, Morgan C, Spillert CR, Kamiyama M, Spolarics Z, Deitch EA, Machiedo GW. Influence of storage on red blood cell rheological properties. J Surg Res. 2002;102(1):6–12. doi: 10.1006/jsre.2001.6306.
  7. Moroz VV, Chernysh AM, Kozlova EK, Sergunova VA, Gudkova OE, Khoroshilov SE, Onufrievich AD, Kostin AI. Disorders in the Morphology and Nanostructure of Erythrocyte Membranes after Long-term Storage of Erythrocyte Suspension: Atomic Force Microscopy Study. Bull Exp Biol Med. 2015;159(3):406–10. doi: 10.1007/s10517-015- 2975-9.
  8. Ciccoli L, De Felice C, Paccagnini E, Leoncini S, Pecorelli A, Signorini C, Belmonte G, Valacchi G, Rossi M, Hayek J. Morphological changes and oxidative damage in Rett Syndrome erythrocytes. Biochim Biophys Acta. 2012;1820(4):511–20. doi: 10.1016/j. bbagen.2011.12.002.
  9. Kozlova EK, Chernysh AM, Moroz VV, Kuzovlev AN. Analysis of nanostructure of red blood cells membranes by space Fourier transform of AFM images. Micron. 2013;44:218– 27. doi: 10.1016/j.micron.2012.06.012.
  10. World Health Organization: Department of Blood Safety and Clinical Technology. The blood cold chain. Guide to the selection and procurement of equipment and accessories. Geneva: World Health Organization; 2002. 61 p.
  11. Karon BS, van Buskirk CM, Jaben EA, Hoyer JD, Thomas DD. Temporal sequence of major biochemical events during blood bank storage of packed red blood cells. Blood Transfus. 2012;10(4):453–61. doi: 10.2450/2012. 0099-11.
  12. Kriebardis AG, Antonelou MH, Stamoulis KE, Economou-Petersen E, Margaritis LH, Papassideri IS. Progressive oxidation of cytoskeletal proteins and accumulation of denatured hemoglobin in stored red cells. J Cell Mol Med. 2007;11(1):148–55. doi: 10.1111/j.1582-4934.2007.00008.x.
  13. Kozlova E, Chernysh A, Moroz V, Gudkova O, Sergunova V, Kuzovlev A. Transformation of membrane nanosurface of red blood cells under hemin action. Sci Rep. 2014;4:6033. doi: 10.1038/srep06033.
  14. Moroz VV, Kirsanova AK, Novodergkina IS, Alexandrin VV, Chernysh AM, Kozlova EK. Macro- and microstructure of erythrocyte membranes under acute massive hemorrhage and subsequent blood reinfusion. Semin Cardiothorac Vasc Anesth. 2010;14(4):248–55. doi: 10.1177/1089253210388518.
  15. Mohandas N, Gallagher PG. Red cell membrane: past, present, and future. Blood. 2008;112(10):3939–48. doi: 10.1182/ blood-2008-07-161166.
  16. Kodippili GC, Spector J, Sullivan C, Kuypers FA, Labotka R, Gallagher PG, Ritchie K, Low PS. Imaging of the diffusion of single band 3 molecules on normal and mutant erythrocytes. Blood. 2009;113(24):6237–45. doi: 10.1182/ blood-2009-02-205450.
  17. Козлова ЕК, Черняев АП, Алексеева ПЮ, Близнюк УА, Черныш AМ, Назарова МА. Диагностика состояния биологических мембран после воздействия γ-излучения в малых дозах. Радиационная биология, радиоэкология. 2005;45(6):653–6.
  18. Chernysh AM, Kozlova EK, Moroz VV. Nanostructure of red blood cell membrane under critical state. Atomic force microscopy and calibrated electroporation. Proceedings of European Summit for Clinical Nanomedicine, 07–09 May 2012, Basel, Switzerland. Basel; 2012. p. 112–3.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2016 Sergunova V.A., Chernyaev A.P., Kozlov A.P., Bliznyuk U.A., Borshchegovskaya P.Y., Kozlova E.K., Chernysh A.M.

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies