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Relationship between red blood cell aggregation and dextran molecular mass

The aim of this study was to investigate the aggregation of red blood cells (RBCs) suspended in dextran solution at various levels of molecular mass. Dextran solutions at molecular mass 40, 70, 100 and 500 kDa at concentration from 2 to 5 g/dL were used to suspend the RBCs. The radius and velocity o...

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Autores principales: Bosek, Maciej, Ziomkowska, Blanka, Pyskir, Jerzy, Wybranowski, Tomasz, Pyskir, Małgorzata, Cyrankiewicz, Michał, Napiórkowska, Marta, Durmowicz, Maciej, Kruszewski, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670059/
https://www.ncbi.nlm.nih.gov/pubmed/36396711
http://dx.doi.org/10.1038/s41598-022-24166-w
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author Bosek, Maciej
Ziomkowska, Blanka
Pyskir, Jerzy
Wybranowski, Tomasz
Pyskir, Małgorzata
Cyrankiewicz, Michał
Napiórkowska, Marta
Durmowicz, Maciej
Kruszewski, Stefan
author_facet Bosek, Maciej
Ziomkowska, Blanka
Pyskir, Jerzy
Wybranowski, Tomasz
Pyskir, Małgorzata
Cyrankiewicz, Michał
Napiórkowska, Marta
Durmowicz, Maciej
Kruszewski, Stefan
author_sort Bosek, Maciej
collection PubMed
description The aim of this study was to investigate the aggregation of red blood cells (RBCs) suspended in dextran solution at various levels of molecular mass. Dextran solutions at molecular mass 40, 70, 100 and 500 kDa at concentration from 2 to 5 g/dL were used to suspend the RBCs. The radius and velocity of sedimenting RBC aggregates were investigated using image analysis. The radius and sedimentation velocity of aggregates increased initially, then decreased after achieving maxima. The maximal velocity of RBC aggregates showed a bell-shaped dependence on dextran molecular mass and concentration, whereas maximal radius showed monotonic increase with both factors. Difference between aggregate and solution density was estimated using aggregate radius and sedimentation velocity and dextran solution viscosity, and was consistent across most molecular mass and concentration levels. This allowed to calculate the porosity of aggregates and to show that it monotonically decreased with the increase in the solution density, caused by the increase in the dextran concentration. The results provide insight into the RBC aggregation process in solutions of proteins of different size, reflecting various pathological conditions. The currently reported data can be potentially applied to specific pathophysiological conditions giving an interpretation that is not yet fully discussed in the literature.
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spelling pubmed-96700592022-11-18 Relationship between red blood cell aggregation and dextran molecular mass Bosek, Maciej Ziomkowska, Blanka Pyskir, Jerzy Wybranowski, Tomasz Pyskir, Małgorzata Cyrankiewicz, Michał Napiórkowska, Marta Durmowicz, Maciej Kruszewski, Stefan Sci Rep Article The aim of this study was to investigate the aggregation of red blood cells (RBCs) suspended in dextran solution at various levels of molecular mass. Dextran solutions at molecular mass 40, 70, 100 and 500 kDa at concentration from 2 to 5 g/dL were used to suspend the RBCs. The radius and velocity of sedimenting RBC aggregates were investigated using image analysis. The radius and sedimentation velocity of aggregates increased initially, then decreased after achieving maxima. The maximal velocity of RBC aggregates showed a bell-shaped dependence on dextran molecular mass and concentration, whereas maximal radius showed monotonic increase with both factors. Difference between aggregate and solution density was estimated using aggregate radius and sedimentation velocity and dextran solution viscosity, and was consistent across most molecular mass and concentration levels. This allowed to calculate the porosity of aggregates and to show that it monotonically decreased with the increase in the solution density, caused by the increase in the dextran concentration. The results provide insight into the RBC aggregation process in solutions of proteins of different size, reflecting various pathological conditions. The currently reported data can be potentially applied to specific pathophysiological conditions giving an interpretation that is not yet fully discussed in the literature. Nature Publishing Group UK 2022-11-17 /pmc/articles/PMC9670059/ /pubmed/36396711 http://dx.doi.org/10.1038/s41598-022-24166-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bosek, Maciej
Ziomkowska, Blanka
Pyskir, Jerzy
Wybranowski, Tomasz
Pyskir, Małgorzata
Cyrankiewicz, Michał
Napiórkowska, Marta
Durmowicz, Maciej
Kruszewski, Stefan
Relationship between red blood cell aggregation and dextran molecular mass
title Relationship between red blood cell aggregation and dextran molecular mass
title_full Relationship between red blood cell aggregation and dextran molecular mass
title_fullStr Relationship between red blood cell aggregation and dextran molecular mass
title_full_unstemmed Relationship between red blood cell aggregation and dextran molecular mass
title_short Relationship between red blood cell aggregation and dextran molecular mass
title_sort relationship between red blood cell aggregation and dextran molecular mass
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670059/
https://www.ncbi.nlm.nih.gov/pubmed/36396711
http://dx.doi.org/10.1038/s41598-022-24166-w
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