Strain-time cell-death threshold for skeletal muscle in a
tissue-engineered model system for deep tissue injury
Strain-time cell-death threshold for skeletal muscle in a
tissue-engineered model system for deep tissue injury
Deep tissue injury (DTI) is a severe pressure ulcer that results from sustained deformation of muscle tissue overlying bony prominences. In order to understand the etiology of DTI, it is essential to determine the tolerance of muscle cells to large mechanical strains. In this study, a new experimental method of determining the time-dependent critical compressive strains for necrotic cell death (E(zz)(c)(t)) in a planar tissue-engineered construct under static loading was developed. A half-spherical indentor is used to induce a non-uniform, concentric distribution of strains in the construct, and E(zz)(c)(t) is calculated from the radius of the damage region in the construct versus time. The method was employed to obtain E(zz)(c)(t) for bio-artificial muscles (BAMs) cultured from C2C12 murine cells, as a model system for DTI. Specifically, propidium iodine was used to fluorescently stain the development of necrosis in BAMs subjected to strains up to 80%. Two groups of BAMs were tested at an extracellular pH of 7.4 (n=10) and pH 6.5 (n=5). The lowest strain levels causing cell death in the BAMs were determined every 15min, during 285-min-long trials, from confocal microscopy fluorescent images of the size of the damage regions. The experimental E(zz)(c)(t) data fitted a decreasing single-step sigmoid of the Boltzmann type. Analysis of the parameters of this sigmoid function indicated a 95% likelihood that cells could tolerate engineering strains below 65% for 1h, whereas the cells could endure strains below 40% over a 285min trial period. The decrease in endurance of the cells to compressive strains occurred between 1-3h post-loading. The method developed in this paper is generic and suitable for studying E(zz)(c)(t) in virtually any planar tissue-engineered construct. The specific E(zz)(c)(t) curve obtained herein is necessary for extrapolating biological damage from muscle-strain data in biomechanical studies of pressure ulcers and DTI
etiology, pressure ulcer, in vitro model, deformation damage, acidosis
2003-2012
Gefen, Amit
85d29654-5b34-472a-91ac-b2a31c590ea9
van Nierop, Bastiaan
b82445a7-a0f0-4cac-8e78-ecc786a37b53
Bader, Dan L.
9884d4f6-2607-4d48-bf0c-62bdcc0d1dbf
Oomens, Cees W.
12b2046f-3a4e-4b14-b1d0-77d48333197a
May 2008
Gefen, Amit
85d29654-5b34-472a-91ac-b2a31c590ea9
van Nierop, Bastiaan
b82445a7-a0f0-4cac-8e78-ecc786a37b53
Bader, Dan L.
9884d4f6-2607-4d48-bf0c-62bdcc0d1dbf
Oomens, Cees W.
12b2046f-3a4e-4b14-b1d0-77d48333197a
Gefen, Amit, van Nierop, Bastiaan, Bader, Dan L. and Oomens, Cees W.
(2008)
Strain-time cell-death threshold for skeletal muscle in a
tissue-engineered model system for deep tissue injury.
Journal of Biomechanics, 41 (9), .
(doi:10.1016/j.jbiomech.2008.03.039).
(PMID:18501912)
Abstract
Deep tissue injury (DTI) is a severe pressure ulcer that results from sustained deformation of muscle tissue overlying bony prominences. In order to understand the etiology of DTI, it is essential to determine the tolerance of muscle cells to large mechanical strains. In this study, a new experimental method of determining the time-dependent critical compressive strains for necrotic cell death (E(zz)(c)(t)) in a planar tissue-engineered construct under static loading was developed. A half-spherical indentor is used to induce a non-uniform, concentric distribution of strains in the construct, and E(zz)(c)(t) is calculated from the radius of the damage region in the construct versus time. The method was employed to obtain E(zz)(c)(t) for bio-artificial muscles (BAMs) cultured from C2C12 murine cells, as a model system for DTI. Specifically, propidium iodine was used to fluorescently stain the development of necrosis in BAMs subjected to strains up to 80%. Two groups of BAMs were tested at an extracellular pH of 7.4 (n=10) and pH 6.5 (n=5). The lowest strain levels causing cell death in the BAMs were determined every 15min, during 285-min-long trials, from confocal microscopy fluorescent images of the size of the damage regions. The experimental E(zz)(c)(t) data fitted a decreasing single-step sigmoid of the Boltzmann type. Analysis of the parameters of this sigmoid function indicated a 95% likelihood that cells could tolerate engineering strains below 65% for 1h, whereas the cells could endure strains below 40% over a 285min trial period. The decrease in endurance of the cells to compressive strains occurred between 1-3h post-loading. The method developed in this paper is generic and suitable for studying E(zz)(c)(t) in virtually any planar tissue-engineered construct. The specific E(zz)(c)(t) curve obtained herein is necessary for extrapolating biological damage from muscle-strain data in biomechanical studies of pressure ulcers and DTI
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Published date: May 2008
Keywords:
etiology, pressure ulcer, in vitro model, deformation damage, acidosis
Organisations:
Medicine
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Local EPrints ID: 169049
URI: http://eprints.soton.ac.uk/id/eprint/169049
ISSN: 0021-9290
PURE UUID: dc21ef08-515e-4516-a7bc-69ed552fc0e5
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Date deposited: 09 Dec 2010 09:02
Last modified: 14 Mar 2024 02:19
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Author:
Amit Gefen
Author:
Bastiaan van Nierop
Author:
Cees W. Oomens
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