Abstract

The ability of membranes of native human red blood cells (RBCs) to bend into the cell to a depth comparable in size with physiological deformations was evaluated. For this, the methods of atomic force microscopy and atomic force spectroscopy were used. Nonlinear patterns of deep deformation (up to 600 nm) of RBC membranes were studied in normal state and under the action of modifiers: fixator (glutaraldehyde), natural oxidant (hemin), and exogenous intoxicator (zinc ions), in vitro. The experimental dependences of membrane bending for control RBC (normal) were approximated by the Hertz model to a depth up to 600 nm. The glutaraldehyde fixator and modifiers increased the absolute value of Young's modulus of membranes and changed the experimental dependences of probe indentation into the cells. Up to some depth hHz, the force curves were approximated by the Hertz model, and for deeper indentations h > hHz, the degree of the polynomial function was changed, the membrane stiffness increased, and the pattern of indentation became another and did not obey the Hertz model. Quantitative characteristics of nonlinear experimental dependences were calculated for deep bending of RBC membranes by approximating them by the degree polynomial function.

Highlights

  • The mechanical properties and structural organization of membranes determine the functional state of red blood cells (RBCs)

  • Changes of the mechanical characteristics of cell membranes can lead to a decrease in the rate of capillary blood flow and to development of stagnant phenomena in the microcirculation, and it can reduce the amount of oxygen delivered to the tissues

  • Elastic properties of RBC membranes, namely, the ability of the membrane to bend into the cell under the action of the applied force, was estimated from empirical force curves

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Summary

Introduction

The mechanical properties and structural organization of membranes determine the functional state of red blood cells (RBCs). Deformability is one of the key physiological and biophysical indicators of RBC [1]. Elastic properties of RBC are largely determined by the stiffness of their membranes and the state of the cytoskeleton lining the inner side of the cell [4]. In studies of RBC membrane stiffness, Young’s modulus is often determined at probe indentation to depths of 10–50 nm [5]. Since RBCs undergo significant deformations in the capillaries, it is of particular interest to study the nonlinear laws of membrane deformation into native cells to depths comparable in size with the values of their physiological deformations (0.5 μm and more)

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