Yield strength of human Erythrocyte membranes to impulsive stretching

Deformability while remaining viable is an important mechanical property of cells. Red blood cells (RBCs) deform considerably while flowing through small capillaries. The RBC membrane can withstand a finite strain, beyond which it ruptures. The classical yield areal strain of 2-4% for RBCs is genera...

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Main Authors: Li, Fenfang, Ohl, Claus-Dieter, Chan, Chon U.
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
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Online Access:https://hdl.handle.net/10356/104612
http://hdl.handle.net/10220/16564
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1046122022-02-16T16:29:25Z Yield strength of human Erythrocyte membranes to impulsive stretching Li, Fenfang Ohl, Claus-Dieter Chan, Chon U. School of Physical and Mathematical Sciences DRNTU::Science::Biological sciences::Human anatomy and physiology Deformability while remaining viable is an important mechanical property of cells. Red blood cells (RBCs) deform considerably while flowing through small capillaries. The RBC membrane can withstand a finite strain, beyond which it ruptures. The classical yield areal strain of 2-4% for RBCs is generally accepted for a quasi-static strain. It has been noted previously that this threshold strain may be much larger with shorter exposure duration. Here we employ an impulse-like forcing to quantify this yield strain of RBC membranes. In the experiments, RBCs are stretched within tens of microseconds by a strong shear flow generated from a laser-induced cavitation bubble. The deformation of the cells in the strongly confined geometry is captured with a high-speed camera and viability is successively monitored with fluorescence microscopy. We find that the probability of cell survival is strongly dependent on the maximum strain. Above a critical areal strain of ~40%, permanent membrane damage is observed for 50% of the cells. Interestingly, many of the cells do not rupture immediately and exhibit ghosting, but slowly obtain a round shape before they burst. This observation is explained with structural membrane damage leading to subnanometer-sized pores. The cells finally lyse from the colloidal osmotic pressure imbalance. 2013-10-17T07:01:34Z 2019-12-06T21:36:14Z 2013-10-17T07:01:34Z 2019-12-06T21:36:14Z 2013 2013 Journal Article Li, F., Chan, C. U., & Ohl, C. (2013). Yield strength of human Erythrocyte membranes to impulsive stretching. Biophysical journal, 105(4), 872-879. 0006-3495 https://hdl.handle.net/10356/104612 http://hdl.handle.net/10220/16564 10.1016/j.bpj.2013.06.045 23972839 en Biophysical journal
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Biological sciences::Human anatomy and physiology
spellingShingle DRNTU::Science::Biological sciences::Human anatomy and physiology
Li, Fenfang
Ohl, Claus-Dieter
Chan, Chon U.
Yield strength of human Erythrocyte membranes to impulsive stretching
description Deformability while remaining viable is an important mechanical property of cells. Red blood cells (RBCs) deform considerably while flowing through small capillaries. The RBC membrane can withstand a finite strain, beyond which it ruptures. The classical yield areal strain of 2-4% for RBCs is generally accepted for a quasi-static strain. It has been noted previously that this threshold strain may be much larger with shorter exposure duration. Here we employ an impulse-like forcing to quantify this yield strain of RBC membranes. In the experiments, RBCs are stretched within tens of microseconds by a strong shear flow generated from a laser-induced cavitation bubble. The deformation of the cells in the strongly confined geometry is captured with a high-speed camera and viability is successively monitored with fluorescence microscopy. We find that the probability of cell survival is strongly dependent on the maximum strain. Above a critical areal strain of ~40%, permanent membrane damage is observed for 50% of the cells. Interestingly, many of the cells do not rupture immediately and exhibit ghosting, but slowly obtain a round shape before they burst. This observation is explained with structural membrane damage leading to subnanometer-sized pores. The cells finally lyse from the colloidal osmotic pressure imbalance.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Li, Fenfang
Ohl, Claus-Dieter
Chan, Chon U.
format Article
author Li, Fenfang
Ohl, Claus-Dieter
Chan, Chon U.
author_sort Li, Fenfang
title Yield strength of human Erythrocyte membranes to impulsive stretching
title_short Yield strength of human Erythrocyte membranes to impulsive stretching
title_full Yield strength of human Erythrocyte membranes to impulsive stretching
title_fullStr Yield strength of human Erythrocyte membranes to impulsive stretching
title_full_unstemmed Yield strength of human Erythrocyte membranes to impulsive stretching
title_sort yield strength of human erythrocyte membranes to impulsive stretching
publishDate 2013
url https://hdl.handle.net/10356/104612
http://hdl.handle.net/10220/16564
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