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2007 Volume No 14
pages 56-63
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Reconstruction of spatially orientated myotubes in
vitro using electrospun, parallel microfibre arrays
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Authors: A Huber, A Pickett, KM Shakesheff
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Address: Wolfson Centre for Stem Cells, Tissue Engineering
and Modelling, The Centre for Biomolecular Sciences, School
of Pharmacy, University of Nottingham, Nottingham, RG7 2RD,
UK
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E-mail: kevin.shakesheff at nottingham.ac.uk
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Key Words: electrospinning, nylon 6/6, scaffold, non-woven
fabric, microstructure, cell culture, C2C12 myoblast, cell
adhesion, differentiation, muscle.
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Publication date: October 8th 2007
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Abstract: The stable culture of myogenic cells and
their differentiation into myotubes in vitro is often
hindered by the mechanical destabilisation of the spontaneously
contractile neotissue formed, resulting in the complete loss
of differentiating myotubes. Electrospun, parallel aligned
nylon 6/6 microfibre arrays were use successfully for the
culture of C2C12 myoblasts and their differentiation to form
mechanically stable, orientated myotubes in vitro.
Myoblasts adhered strongly to the parallel fibre array, forming
a compact cell sheath across the entire array, aligning individual
cells in parallel to the direction of the fibrous substratum.
The myogenic potential of C2C12 myoblasts was not impaired
and resulted in the formation of elongated myotubes expressing
alpha-actinin, adult myosin heavy chain and nicotinic acetylcholine
receptors as muscle-specific marker proteins. Newly formed
C2C12 myotubes were themselves orientated in parallel to the
direction of the underlying fibrous substratum and exhibited
a high level of structural integration with the surrounding
cells. In contrast, non-woven, non-orientated nylon 6/6 meshes,
produced by conventional electrospinning, exhibited greatly
reduced levels of C2C12 myoblast attachment and adherent myoblasts
did not differentiate into myotubes. In conclusion, parallel
microfibre arrays provided a superior microscale topography
for the stable maintenance and differentiation of myotubes
in vitro.
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