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Dynamics of Individual Red Blood Cells Under Shear Flow: A Way to Discriminate Deformability Alterations

In this work, we compared the dynamics of motion in a linear shear flow of individual red blood cells (RBCs) from healthy and pathological donors (Sickle Cell Disease (SCD) or Sickle Cell-β-thalassemia) and of low and high densities, in a suspending medium of higher viscosity. In these conditions, a...

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Autores principales: Atwell, Scott, Badens, Catherine, Charrier, Anne, Helfer, Emmanuèle, Viallat, Annie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767062/
https://www.ncbi.nlm.nih.gov/pubmed/35069240
http://dx.doi.org/10.3389/fphys.2021.775584
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author Atwell, Scott
Badens, Catherine
Charrier, Anne
Helfer, Emmanuèle
Viallat, Annie
author_facet Atwell, Scott
Badens, Catherine
Charrier, Anne
Helfer, Emmanuèle
Viallat, Annie
author_sort Atwell, Scott
collection PubMed
description In this work, we compared the dynamics of motion in a linear shear flow of individual red blood cells (RBCs) from healthy and pathological donors (Sickle Cell Disease (SCD) or Sickle Cell-β-thalassemia) and of low and high densities, in a suspending medium of higher viscosity. In these conditions, at lower shear rates, biconcave discocyte-shaped RBCs present an unsteady flip-flopping motion, where the cell axis of symmetry rotates in the shear plane, rocking to and fro between an orbital angle ±ϕ observed when the cell is on its edge. We show that the evolution of ϕ depends solely on RBC density for healthy RBCs, with denser RBCs displaying lower ϕ values than the lighter ones. Typically, at a shear stress of 0.08 Pa, ϕ has values of 82 and 72° for RBCs with average densities of 1.097 and 1.115, respectively. Surprisingly, we show that SCD RBCs display the same ϕ-evolution as healthy RBCs of same density, showing that the flip-flopping behavior is unaffected by the SCD pathology. When the shear stress is increased further (above 0.1 Pa), healthy RBCs start going through a transition to a fluid-like motion, called tank-treading, where the RBC has a quasi-constant orientation relatively to the flow and the membrane rotates around the center of mass of the cell. This transition occurs at higher shear stresses (above 0.2 Pa) for denser cells. This shift toward higher stresses is even more remarkable in the case of SCD RBCs, showing that the transition to the tank-treading regime is highly dependent on the SCD pathology. Indeed, at a shear stress of 0.2 Pa, for RBCs with a density of 1.097, 100% of healthy RBCs have transited to the tank-treading regime vs. less than 50% SCD RBCs. We correlate the observed differences in dynamics to the alterations of RBC mechanical properties with regard to density and SCD pathology reported in the literature. Our results suggest that it might be possible to develop simple non-invasive assays for diagnosis purpose based on the RBC motion in shear flow and relying on this millifluidic approach.
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spelling pubmed-87670622022-01-20 Dynamics of Individual Red Blood Cells Under Shear Flow: A Way to Discriminate Deformability Alterations Atwell, Scott Badens, Catherine Charrier, Anne Helfer, Emmanuèle Viallat, Annie Front Physiol Physiology In this work, we compared the dynamics of motion in a linear shear flow of individual red blood cells (RBCs) from healthy and pathological donors (Sickle Cell Disease (SCD) or Sickle Cell-β-thalassemia) and of low and high densities, in a suspending medium of higher viscosity. In these conditions, at lower shear rates, biconcave discocyte-shaped RBCs present an unsteady flip-flopping motion, where the cell axis of symmetry rotates in the shear plane, rocking to and fro between an orbital angle ±ϕ observed when the cell is on its edge. We show that the evolution of ϕ depends solely on RBC density for healthy RBCs, with denser RBCs displaying lower ϕ values than the lighter ones. Typically, at a shear stress of 0.08 Pa, ϕ has values of 82 and 72° for RBCs with average densities of 1.097 and 1.115, respectively. Surprisingly, we show that SCD RBCs display the same ϕ-evolution as healthy RBCs of same density, showing that the flip-flopping behavior is unaffected by the SCD pathology. When the shear stress is increased further (above 0.1 Pa), healthy RBCs start going through a transition to a fluid-like motion, called tank-treading, where the RBC has a quasi-constant orientation relatively to the flow and the membrane rotates around the center of mass of the cell. This transition occurs at higher shear stresses (above 0.2 Pa) for denser cells. This shift toward higher stresses is even more remarkable in the case of SCD RBCs, showing that the transition to the tank-treading regime is highly dependent on the SCD pathology. Indeed, at a shear stress of 0.2 Pa, for RBCs with a density of 1.097, 100% of healthy RBCs have transited to the tank-treading regime vs. less than 50% SCD RBCs. We correlate the observed differences in dynamics to the alterations of RBC mechanical properties with regard to density and SCD pathology reported in the literature. Our results suggest that it might be possible to develop simple non-invasive assays for diagnosis purpose based on the RBC motion in shear flow and relying on this millifluidic approach. Frontiers Media S.A. 2022-01-05 /pmc/articles/PMC8767062/ /pubmed/35069240 http://dx.doi.org/10.3389/fphys.2021.775584 Text en Copyright © 2022 Atwell, Badens, Charrier, Helfer and Viallat. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Atwell, Scott
Badens, Catherine
Charrier, Anne
Helfer, Emmanuèle
Viallat, Annie
Dynamics of Individual Red Blood Cells Under Shear Flow: A Way to Discriminate Deformability Alterations
title Dynamics of Individual Red Blood Cells Under Shear Flow: A Way to Discriminate Deformability Alterations
title_full Dynamics of Individual Red Blood Cells Under Shear Flow: A Way to Discriminate Deformability Alterations
title_fullStr Dynamics of Individual Red Blood Cells Under Shear Flow: A Way to Discriminate Deformability Alterations
title_full_unstemmed Dynamics of Individual Red Blood Cells Under Shear Flow: A Way to Discriminate Deformability Alterations
title_short Dynamics of Individual Red Blood Cells Under Shear Flow: A Way to Discriminate Deformability Alterations
title_sort dynamics of individual red blood cells under shear flow: a way to discriminate deformability alterations
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767062/
https://www.ncbi.nlm.nih.gov/pubmed/35069240
http://dx.doi.org/10.3389/fphys.2021.775584
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