Author:
Voytik-Harbin Sherry L.,Roeder Blayne A.,Sturgis Jennifer E.,Kokini Klod,Robinson J. Paul
Abstract
At present, mechanisms by which specific structural and mechanical
properties of the three-dimensional extracellular matrix
microenvironment influence cell behavior are not known. Lack
of such knowledge precludes formulation of engineered scaffolds
or tissue constructs that would deliver specific growth-inductive
signals required for improved tissue restoration. This article
describes a new mechanical loading–imaging technique that
allows investigations of structural–mechanical properties
of biomaterials as well as the structural–mechanical basis
of cell–scaffold interactions at a microscopic level and
in three dimensions. The technique is based upon the integration
of a modified, miniature mechanical loading instrument with
a confocal microscope. Confocal microscopy is conducted in a
reflection and/or fluorescence mode for selective visualization
of load-induced changes to the scaffold and any resident cells,
while maintaining each specimen in a “live,” fully
hydrated state. This innovative technique offers several advantages
over current biomechanics methodologies, including simultaneous
visualization of scaffold and/or cell microstructure in
three dimensions during mechanical loading; quantification of
macroscopic mechanical parameters including true stress and
strain; and the ability to perform multiple analyses on the
same specimen. This technique was used to determine the
structural–mechanical properties of three very different
biological materials: a reconstituted collagen matrix, a
tissue-derived biomaterial, and a tissue construct representing
cells and matrix.
Publisher
Cambridge University Press (CUP)
Cited by
65 articles.
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