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  4. Mechanical property quantification of endothelial cells using scanning acoustic microscopy
 
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2012
Conference Paper
Title

Mechanical property quantification of endothelial cells using scanning acoustic microscopy

Abstract
The mechanical properties of cells reflect dynamic changes of cellular organization which occur during physiologic activities like cell movement, cell volume regulation or cell division. Thus the study of cell mechanical properties can yield important information for understanding these physiologic activities. Endothelial cells form the thin inner lining of blood vessels in the cardiovascular system and are thus exposed to shear stress as well as tensile stress caused by the pulsatile blood flow. Endothelial dysfunction might occur due to reduced resistance to mechanical stress and is an initial step in the development of cardiovascular disease like, e.g., atherosclerosis. Therefore we investigated the mechanical properties of primary human endothelial cells (HUVEC) of different age using scanning acoustic microscopy at 1.2 GHz. The HUVECs are classified as young (t D < 90 h) and old (t D > 90 h) cells depending upon the generation time for the population doubling of the culture (t D). Longitudinal sound velocity and geometrical properties of cells (thickness) were determined using the material signature curve V(z) method for variable culture condition along spatial coordinates. The plane wave technique with normal incidence is assumed to solve two-dimensional wave equation. The size of the cells is modeled using multilayered (solid-fluid) system. The propagation of transversal wave and surface acoustic wave are neglected in soft matter analysis. The biomechanical properties of HUVEC cells are quantified in an age dependent manner.
Author(s)
Shelke, A.
Brand, S.
Kundu, T.
Bereiter-Hahn, J.
Blasé, C.
Mainwork
Health monitoring of structural and biological systems 2012  
Conference
Conference on Health Monitoring of Structural and Biological Systems 2012  
DOI
10.1117/12.917512
Language
English
IWM-H  
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