Investigation of bone resorption within a cortical basic multicellular unit using a lattice-based computational model

被引:20
作者
Buenzli, Pascal R. [2 ]
Jeon, Junhwan [1 ]
Pivonka, Peter [2 ]
Smith, David W. [2 ]
Cummings, Peter T. [1 ,3 ]
机构
[1] Vanderbilt Univ, Dept Chem & Biomol Engn, Nashville, TN 37235 USA
[2] Univ Western Australia, Fac Engn Comp & Math, Nedlands, WA 6009, Australia
[3] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
基金
澳大利亚研究理事会; 美国国家科学基金会;
关键词
Bone resorption; Basic Multicellular Units (BMU); Osteoclast-bone interaction; Osteoclast fusion; Computational model; CELLULAR-AUTOMATON; TUMOR-GROWTH; IN-VITRO; OSTEON; CELLS; OSTEOCLASTS; DYNAMICS; KINETICS; ADHESION; DRIVEN;
D O I
10.1016/j.bone.2011.10.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this paper we develop a lattice-based computational model focused on bone resorption by osteoclasts in a single cortical basic multicellular unit (BMU). Our model takes into account the interaction of osteoclasts with the bone matrix, the interaction of osteoclasts with each other, the generation of osteoclasts from a growing blood vessel, and the renewal of osteoclast nuclei by cell fusion. All these features are shown to strongly influence the geometrical properties of the developing resorption cavity including its size, shape and progression rate, and are also shown to influence the distribution, resorption pattern and trajectories of individual osteoclasts within the BMU. We demonstrate that for certain parameter combinations, resorption cavity shapes can be recovered from the computational model that closely resemble resorption cavity shapes observed from microCT imaging of human cortical bone. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:378 / 389
页数:12
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