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contributor authorGerard A. Ateshian
contributor authorKevin D. Costa
contributor authorBarclay Morrison
contributor authorClark T. Hung
contributor authorEvren U. Azeloglu
date accessioned2017-05-09T00:31:29Z
date available2017-05-09T00:31:29Z
date copyrightOctober, 2009
date issued2009
identifier issn0148-0731
identifier otherJBENDY-27048#101001_1.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/139831
description abstractA framework is formulated within the theory of mixtures for continuum modeling of biological tissue growth that explicitly addresses cell division, using a homogenized representation of cells and their extracellular matrix (ECM). The model relies on the description of the cell as containing a solution of water and osmolytes, and having a porous solid matrix. The division of a cell into two nearly identical daughter cells is modeled as the doubling of the cell solid matrix and osmolyte content, producing an increase in water uptake via osmotic effects. This framework is also generalized to account for the growth of ECM-bound molecular species that impart a fixed charge density (FCD) to the tissue, such as proteoglycans. This FCD similarly induces osmotic effects, resulting in extracellular water uptake and osmotic pressurization of the ECM interstitial fluid, with concomitant swelling of its solid matrix. Applications of this growth model are illustrated in several examples.
publisherThe American Society of Mechanical Engineers (ASME)
titleContinuum Modeling of Biological Tissue Growth by Cell Division, and Alteration of Intracellular Osmolytes and Extracellular Fixed Charge Density
typeJournal Paper
journal volume131
journal issue10
journal titleJournal of Biomechanical Engineering
identifier doi10.1115/1.3192138
journal fristpage101001
identifier eissn1528-8951
keywordsDensity
keywordsBiological tissues
keywordsMixtures
keywordsModeling
keywordsMembranes AND Water
treeJournal of Biomechanical Engineering:;2009:;volume( 131 ):;issue: 010
contenttypeFulltext


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