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• W2079402289 endingPage "708" @default.
• W2079402289 startingPage "699" @default.
• W2079402289 abstract "The ability to create extracellular matrix (ECM) constructs that are mechanically and biochemically similar to those found in vivo and to understand how their properties affect cellular responses will drive the next generation of tissue engineering strategies. To date, many mechanisms by which cells biochemically communicate with the ECM are known. However, the mechanisms by which mechanical information is transmitted between cells and their ECM remain to be elucidated. “Self-assembled” collagen matrices provide an in vitro-model system to study the mechanical behavior of ECM. To begin to understand how the ECM and the cells interact mechanically, the three-dimensional (3D) mechanical properties of the ECM must be quantified at the micro-(local) level in addition to information measured at the macro-(global) level. Here we describe an incremental digital volume correlation (IDVC) algorithm to quantify large (>0.05) 3D mechanical strains in the microstructure of 3D collagen matrices in response to applied mechanical loads. Strain measurements from the IDVC algorithm rely on 3D confocal images acquired from collagen matrices under applied mechanical loads. The accuracy and the precision of the IDVC algorithm was verified by comparing both image volumes collected in succession when no deformation was applied to the ECM (zero strain) and image volumes to which simulated deformations were applied in both 1D and 3D (simulated strains). Results indicate that the IDVC algorithm can accurately and precisely determine the 3D strain state inside largely deformed collagen ECMs. Finally, the usefulness of the algorithm was demonstrated by measuring the microlevel 3D strain response of a collagen ECM loaded in tension." @default.
• W2079402289 created "2016-06-24" @default.
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• W2079402289 date "2004-12-01" @default.
• W2079402289 modified "2023-10-17" @default.
• W2079402289 title "Local, Three-Dimensional Strain Measurements Within Largely Deformed Extracellular Matrix Constructs" @default.
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• W2079402289 doi "https://doi.org/10.1115/1.1824127" @default.
• W2079402289 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15796328" @default.
• W2079402289 hasPublicationYear "2004" @default.
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