Mechanical Characterization of the Erythrocyte Membrane Using a Capacitor-Based Technique

Pathological processes often change the mechanical properties of cells. Increased rigidity could be a marker of cellular malfunction. Erythrocytes are a type of cell that deforms to squeeze through tiny capillaries; changes in their rigidity can dramatically affect their functionality. Furthermore,...

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Veröffentlicht in:Micromachines (Basel) 2024-05, Vol.15 (5), p.590
Hauptverfasser: Dorta, Doriana, Plazaola, Carlos, Carrasco, Jafeth, Alves-Rosa, Maria F, Coronado, Lorena M, Correa, Ricardo, Zambrano, Maytee, Gutiérrez-Medina, Braulio, Sarmiento-Gómez, Erick, Spadafora, Carmenza, Gonzalez, Guadalupe
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Sprache:eng
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Zusammenfassung:Pathological processes often change the mechanical properties of cells. Increased rigidity could be a marker of cellular malfunction. Erythrocytes are a type of cell that deforms to squeeze through tiny capillaries; changes in their rigidity can dramatically affect their functionality. Furthermore, differences in the homeostatic elasticity of the cell can be used as a tool for diagnosis and even for choosing the adequate treatment for some illnesses. More accurate types of equipment needed to study biomechanical phenomena at the single-cell level are very costly and thus out of reach for many laboratories around the world. This study presents a simple and low-cost technique to study the rigidity of red blood cells (RBCs) through the application of electric fields in a hand-made microfluidic chamber that uses a capacitor principle. As RBCs are deformed with the application of voltage, cells are observed under a light microscope. From mechanical force vs. deformation data, the elastic constant of the cells is determined. The results obtained with the capacitor-based method were compared with those obtained using optical tweezers, finding good agreement. In addition, -infected erythrocytes were tested with the electric field applicator. Our technique provides a simple means of testing the mechanical properties of individual cells.
ISSN:2072-666X
2072-666X
DOI:10.3390/mi15050590