The development of anisotropic mechanical properties is critical for the successful function of many soft tissues. Load bearing tissues naturally develop varying degrees of anisotropy, presumably in response to their specific loading environment. For example, the scar tissue that forms after a myocardial infarction is structurally and mechanically anisotropic. To better understand the scar mechanics, we first need to develop structure-function relationships for collagen fiber networks. In order to improve the healing after myocardial infarction, a better understanding of the mechanical anisotropy is necessary. An in vitro collagen gel system can be used to control individual fiber network components and to determine the effect of each component on the mechanical properties of the gel. Previously, we demonstrated the ability to promote two different collagen gel structures, with two different levels of mechanical anisotropy [1]. The goal of the current study was to quantitatively relate the observed mechanical anisotropy to the collagen fiber structure. It was hypothesized that the anisotropy could be explained with a simple structural model, where the gel behavior is derived from the behavior of the individual fibers within the gel (i.e., the properties of the fibers, their orientation, and their level of slack).
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ASME 2004 International Mechanical Engineering Congress and Exposition
November 13–19, 2004
Anaheim, California, USA
Conference Sponsors:
- Bioengineering Division
ISBN:
0-7918-4703-9
PROCEEDINGS PAPER
A Structural Basis for Anisotropy in Cardiac Fibroblast Populated Collagen Gels
Stavros Thomopoulos,
Stavros Thomopoulos
Columbia University
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Jeffrey W. Holmes
Jeffrey W. Holmes
Columbia University
Search for other works by this author on:
Stavros Thomopoulos
Columbia University
Jeffrey W. Holmes
Columbia University
Paper No:
IMECE2004-61209, pp. 305-306; 2 pages
Published Online:
March 24, 2008
Citation
Thomopoulos, S, & Holmes, JW. "A Structural Basis for Anisotropy in Cardiac Fibroblast Populated Collagen Gels." Proceedings of the ASME 2004 International Mechanical Engineering Congress and Exposition. Advances in Bioengineering. Anaheim, California, USA. November 13–19, 2004. pp. 305-306. ASME. https://doi.org/10.1115/IMECE2004-61209
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