Sickle cell trait human erythrocytes are significantly stiffer than normal.

Abstract

Atomic force microscopy (AFM) allows for high-resolution topography studies of biological cells and measurement of their mechanical properties in physiological conditions. In this work, AFM was employed to measure the stiffness of abnormal human red blood cells from human subjects with the genotype for sickle cell trait. The determined Young's modulus was compared with that obtained from measurements of erythrocytes from healthy subjects. The results showed that Young's modulus of pathological erythrocytes was approximately three times higher than in normal cells. Observed differences indicate the effect of the polymerization of sickle hemoglobin as well as possible changes in the organization of the cell cytoskeleton associated with the sickle cell trait.

• Authors: Jamie L Maciaszek, George Lykotrafitis
• Journal: Journal of biomechanics (J Biomech) Vol. 44 Issue 4 Pg. 657-61 (Feb 24 2011) ISSN: 1873-2380 [Electronic] United States
• PMID: 21111421 (Publication Type: Comparative Study, Journal Article)
• Copyright: Copyright © 2010 Elsevier Ltd. All rights reserved.

Topics

• Cells, Cultured
• Compressive Strength
• Elastic Modulus
• Erythrocytes, Abnormal (pathology, physiology)
• Hardness
• Humans
• Sickle Cell Trait (pathology, physiopathology)
• Stress, Mechanical
• Tensile Strength