Hemoglobin Binding to the Red Blood Cell (RBC) Membrane Is Associated with Decreased Cell Deformability

Author:

Barshtein Gregory1ORCID,Livshits Leonid2,Gural Alexander3,Arbell Dan4,Barkan Refael5,Pajic-Lijakovic Ivana6ORCID,Yedgar Saul1

Affiliation:

1. Department of Biochemistry, The Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 9112001, Israel

2. Red Blood Cell Research Group, Vetsuisse Faculty, Institute of Veterinary Physiology, University of Zurich, 8057 Zürich, Switzerland

3. Blood Bank, Hadassah University Hospital, Jerusalem 9112001, Israel

4. Pediatric Surgery, Hadassah University Hospital, Jerusalem 9112001, Israel

5. Department of Digital Medical Technologies, Holon Institute of Technology, Holon 5810201, Israel

6. Department of Chemical Engineering, University of Belgrade, 11000 Belgrade, Serbia

Abstract

The deformability of red blood cells (RBCs), expressing their ability to change their shape as a function of flow-induced shear stress, allows them to optimize oxygen delivery to the tissues and minimize their resistance to flow, especially in microcirculation. During physiological aging and blood storage, or under external stimulations, RBCs undergo metabolic and structural alterations, one of which is hemoglobin (Hb) redistribution between the cytosol and the membrane. Consequently, part of the Hb may attach to the cell membrane, and although this process is reversible, the increase in membrane-bound Hb (MBHb) can affect the cell’s mechanical properties and deformability in particular. In the present study, we examined the correlation between the MBHb levels, determined by mass spectroscopy, and the cell deformability, determined by image analysis. Six hemoglobin subunits were found attached to the RBC membranes. The cell deformability was negatively correlated with the level of four subunits, with a highly significant inter-correlation between them. These data suggest that the decrease in RBC deformability results from Hb redistribution between the cytosol and the cell membrane and the respective Hb interaction with the cell membrane.

Funder

Hebrew University internal

Publisher

MDPI AG

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