Nano-microscale models of periosteocytic flow show differences in stresses imparted to cell body and processes

被引:73
作者
Anderson, EJ
Kaliyamoorthy, S
Alexander, JID
Tate, MLK
机构
[1] Case Western Reserve Univ, Dept Mech & Aerosp Engn, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[3] Cleveland Clin Fdn ND20, Orthopaed Res Ctr, Cleveland, OH USA
关键词
computational fluid dynamics; bone; shear; pressure; lacunocanalicular; lacuna; canaliculus; osteocyte; mechanotransduction; subcellular domains;
D O I
10.1007/s10439-005-8962-y
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In order to understand how local changes in mechanical environment are translated into cellular activity underlying tissue level bone adaptation, there is a need to explore fluid flow regimes at small scales such as the osteocyte. Recent developments in computational fluid dynamics (CFD) provide impetus to elucidate periosteocytic flow through development of a nano-microscale model to study local effects of fluid flow on the osteocyte cell body, which contains the cellular organelles, and on the osteocyte processes, which connect the cell to the entire cellular network distributed throughout bone tissue. For each model, fluid flow was induced via a pressure gradient and the velocity profile and wall shear stress at the cell-fluid interface were calculated using a CFD software package designed for nano/micro-electromechanical-systems device development. Periosteocytic flow was modeled, taking into consideration the nanoscale dimensions of the annular channels and the flow pathways of the periosteocytic flow volume, to analyze the local effects of fluid flow on the osteocyte cell body (within the lacuna) and its processes (within the canaliculi). Based on the idealized model presented in this article, the osteocyte cell body is exposed primarily to effects of hydrodynamic pressure and the cell processes (CP) are exposed primarily to fluid shear stress, with highest stress gradients at sites where the process meets the cell body and where two CP link at the gap junction. Hence, this model simulates subcellular effects of fluid flow and suggests, for the first time to our knowledge, major differences in modes of loading between the domain of the cell body and that of the cell process.
引用
收藏
页码:52 / 62
页数:11
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