DocumentCode :
2116484
Title :
Virtual experiments of heart valve tissues
Author :
Siyao Huang ; Huang, Hsiao-Ying S.
Author_Institution :
Dept. of Mech. & Aerosp. Eng., North Carolina State Univ., Raleigh, NC, USA
fYear :
2012
fDate :
Aug. 28 2012-Sept. 1 2012
Firstpage :
6645
Lastpage :
6648
Abstract :
The heart valve tissue mainly contains collagen fibers and valve interstitial cells (VICs) and constantly experiences different stress states during cardiac cycles. Due to the anisotropic architecture of collagen fibers and highly inhomogeneous cell population, the mechanical behavior of the heart valve becomes more complicated. It is known that external mechanical stimuli can lead to extracellular matrix (ECM) remodeling, cellular mechanotransduction, cell migration, and collagen synthesis; however, the mechanism of matrix-to-cell stress transfer remains unclear. Current study presents heterogeneously distributed collagen fibers responsible for transmitting forces into cells by an image-based finite element analysis incorporating histological photomicrographs of porcine heart valve tissues. Besides, nonlinear and anisotropic material properties tissue models are incorporated to quantify and visualize the overall stress distributions in heart valve tissues. By establishing an effectively predictive method with new computational tools and by performing virtual experiments on the heart valves, the role of load transmission in heart valves is clarified. The current study completely illustrates the stress distribution around cells and demonstrates the force transmission and reception between cells and matrix in the heart valve tissue. Therefore, our developed image-based finite element models provide new insights not only into clarifying the role of the force transmission and reception between heterogeneously distributed collagen fibers, but also a better understanding of relationships between the mechanical stimuli, cellular mechanotransduction, cell migration, matrix synthesis, and tissue remodeling in heart valves.
Keywords :
biology computing; biomechanics; biomedical optical imaging; cardiology; cell motility; cellular biophysics; finite element analysis; physiological models; proteins; stress effects; ECM remodeling; VIC; anisotropic material properties; cardiac cycles; cell migration; cellular mechanotransduction; collagen fiber anisotropic architecture; collagen synthesis; external mechanical stimuli; extracellular matrix remodeling; force reception; force transmission; heart valve mechanical behavior; heart valve tissue stress distribution; heart valve tissues; heterogeneously distributed collagen fibers; histological photomicrographs; image based finite element analysis; inhomogeneous cell population; load transmission; matrix synthesis; matrix-cell stress transfer mechanism; nonlinear material properties; porcine heart valve tissue model; stress states; tissue remodeling; valve interstitial cells; virtual experiments; Biomechanics; Electronic countermeasures; Heart; Material properties; Microstructure; Stress; Valves; Animals; Biomechanical Phenomena; Cell Movement; Collagen; Computational Biology; Computer Simulation; Extracellular Matrix; Finite Element Analysis; Heart; Heart Valve Prosthesis; Heart Valves; Humans; Mechanotransduction, Cellular; Models, Cardiovascular; Swine;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Engineering in Medicine and Biology Society (EMBC), 2012 Annual International Conference of the IEEE
Conference_Location :
San Diego, CA
ISSN :
1557-170X
Print_ISBN :
978-1-4244-4119-8
Electronic_ISBN :
1557-170X
Type :
conf
DOI :
10.1109/EMBC.2012.6347518
Filename :
6347518
Link To Document :
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