Effect of Cell Age and Membrane Rigidity on Red Blood Cell Shape in Capillary Flow

Cells. 2023 Jun 1;12(11):1529. doi: 10.3390/cells12111529.

Abstract

Blood flow in the microcirculatory system is crucially affected by intrinsic red blood cell (RBC) properties, such as their deformability. In the smallest vessels of this network, RBCs adapt their shapes to the flow conditions. Although it is known that the age of RBCs modifies their physical properties, such as increased cytosol viscosity and altered viscoelastic membrane properties, the evolution of their shape-adapting abilities during senescence remains unclear. In this study, we investigated the effect of RBC properties on the microcapillary in vitro flow behavior and their characteristic shapes in microfluidic channels. For this, we fractioned RBCs from healthy donors according to their age. Moreover, the membranes of fresh RBCs were chemically rigidified using diamide to study the effect of isolated graded-membrane rigidity. Our results show that a fraction of stable, asymmetric, off-centered slipper-like cells at high velocities decreases with increasing age or diamide concentration. However, while old cells form an enhanced number of stable symmetric croissants at the channel centerline, this shape class is suppressed for purely rigidified cells with diamide. Our study provides further knowledge about the distinct effects of age-related changes of intrinsic cell properties on the single-cell flow behavior of RBCs in confined flows due to inter-cellular age-related cell heterogeneity.

Keywords: cell shape; density separation; diamide; erythrocyte; membrane rigidity; microcirculation; microfluidics; red blood cell senescence; red blood cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Diamide* / pharmacology
  • Erythrocyte Deformability* / physiology
  • Erythrocytes
  • Microcirculation
  • Microfluidics

Substances

  • Diamide

Grants and funding

This work was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)—project number 349558021 (LA 2682/9-1, WA 1336/13-1, and RE 5025/1-2), and by the Marie Skłodowska-Curie grant agreement no. 860436—EVIDENCE. M.N. acknowledges support and funding from the “Deutsch-Französische-Hochschule” (DFH) DFDK CDFA-01-14 “Living fluids”. A.D. acknowledges funding from the Young Investigator Grant of Saarland University. The authors acknowledge support by Saarland University within the “Open Access Publication Funding” program.