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Skeletal myogenesis on highly orientated microfibrous polyesterurethane scaffolds
Skeletal myogenesis is a complex process, which is known to be intimately depending on an optimal outside‐in substrate‐cell signaling. Current attempts to reproduce skeletal muscle tissue in vitro using traditional scaffolds mainly suffer from poor directionality of the myofibers, resulting in an in...
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Published in: | Journal of biomedical materials research. Part A 2008-03, Vol.84A (4), p.1094-1101 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Skeletal myogenesis is a complex process, which is known to be intimately depending on an optimal outside‐in substrate‐cell signaling. Current attempts to reproduce skeletal muscle tissue in vitro using traditional scaffolds mainly suffer from poor directionality of the myofibers, resulting in an ineffective vectorial power generation. In this study, we aimed at investigating skeletal myogenesis on novel biodegradable microfibrous scaffolds made of DegraPol®, a block polyesterurethane previously demonstrated to be suitable for this application. DegraPol® was processed by electrospinning in the form of highly orientated (“O”) and nonorientated (“N/O”) microfibrous meshes and by solvent‐casting in the form of nonporous films (“F”). The effect of the fiber orientation at the scaffold surface was evaluated by investigating C2C12 and L6 proliferation (via SEM analysis and alamarBlue™ test) and differentiation (via RT‐PCR analysis and MHC immunostaining). We demonstrated that highly orientated elastomeric microfibrous DegraPol® scaffolds enable skeletal myogenesis in vitro by aiding in (a) myoblast adhesion, (b) myotube alignment, and (c) noncoplanar arrangement of cells, by providing the necessary directional cues along with architectural and mechanical support. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res, 2008 |
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ISSN: | 1549-3296 1552-4965 |
DOI: | 10.1002/jbm.a.31534 |