Combined Technologies for Microfabricating Elastomeric Cardiac Tissue Engineering Scaffolds
β Scribed by Maxime D. Guillemette; Hyoungshin Park; James C. Hsiao; Saloni R. Jain; Benjamin L. Larson; Robert Langer; Lisa E. Freed
- Book ID
- 102933892
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 949 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1616-5187
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Polymer scaffolds that direct elongation and orientation of cultured cells can enable tissue engineered muscle to act as a mechanically functional unit. We combined micromolding and microablation technologies to create muscle tissue engineering scaffolds from the biodegradable elastomer poly(glycerol sebacate). These scaffolds exhibited well defined surface patterns and pores and robust elastomeric tensile mechanical properties. Cultured C2C12 muscle cells penetrated the pores to form spatially controlled engineered tissues. Scanning electron and confocal microscopy revealed muscle cell orientation in a preferential direction, parallel to micromolded gratings and long axes of microablated anisotropic pores, with significant individual and interactive effects of gratings and pore design.
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## Abstract Native myocardium consists of several cell types, of which approximately oneβthird are myocytes and most of the nonmyocytes are fibroblasts. By analogy with monolayer culture in which fibroblasts were removed to prevent overgrowth, early attempts to engineer myocardium utilized cell pop