Controlling the orientation and synaptic differentiation of myotubes with micropatterned substrates.

Micropatterned poly(dimethylsiloxane) substrates fabricated by soft lithography led to large-scale orientation of myoblasts in culture, thereby controlling the orientation of the myotubes they formed. Fusion occurred on many chemically identical surfaces in which varying structures were arranged in square or hexagonal lattices, but only a subset of patterned surfaces yielded aligned myotubes. Remarkably, on some substrates, large populations of myotubes oriented at a reproducible acute angle to the lattice of patterned features. A simple geometrical model predicts the angle and extent of orientation based on maximizing the contact area between the myoblasts and patterned topographic surfaces. Micropatterned substrates also provided short-range cues that influenced higher-order functions such as the localization of focal adhesions and accumulation of postsynaptic acetylcholine receptors. Our results represent what we believe is a new approach for musculoskeletal tissue engineering, and our model sheds light on mechanisms of myotube alignment in vivo.

[1]  P. Purslow,et al.  Differentiation of Myoblasts in Serum-Free Media: Effects of Modified Media Are Cell Line-Specific , 2000, Cells Tissues Organs.

[2]  J. Y. Lim,et al.  Cell sensing and response to micro- and nanostructured surfaces produced by chemical and topographic patterning. , 2007, Tissue engineering.

[3]  G. Pavlath,et al.  Molecular control of mammalian myoblast fusion. , 2008, Methods in molecular biology.

[4]  C. Marcelle,et al.  WNT11 acts as a directional cue to organize the elongation of early muscle fibres , 2009, Nature.

[5]  H. Blau,et al.  Plasticity of the differentiated state. , 1985, Science.

[6]  S. Lowen The Biophysical Journal , 1960, Nature.

[7]  P. De Camilli,et al.  A role for talin in presynaptic function , 2004, The Journal of cell biology.

[8]  Benjamin Chu,et al.  Myotube assembly on nanofibrous and micropatterned polymers. , 2006, Nano letters.

[9]  J. Sanes,et al.  Development of the vertebrate neuromuscular junction. , 1999, Annual review of neuroscience.

[10]  E. Hay,et al.  Cell Biology of Extracellular Matrix , 1988, Springer US.

[11]  Joe Tien,et al.  Mechanotransduction at cell-matrix and cell-cell contacts. , 2004, Annual review of biomedical engineering.

[12]  J. Lammerding,et al.  Nuclear Shape, Mechanics, and Mechanotransduction , 2008, Circulation research.

[13]  K. Hjort,et al.  Myotube Formation on Micro-patterned Glass: Intracellular Organization and Protein Distribution in C2C12 Skeletal Muscle Cells , 2008, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[14]  Terrance T. Kummer,et al.  Nerve-independent formation of a topologically complex postsynaptic apparatus , 2004, The Journal of cell biology.

[15]  Hansong Zeng,et al.  Fabrication of skeletal muscle constructs by topographic activation of cell alignment , 2009, Biotechnology and bioengineering.

[16]  G. Whitesides,et al.  Patterning proteins and cells using soft lithography. , 1999, Biomaterials.

[17]  J. Sanes,et al.  Laminins promote postsynaptic maturation by an autocrine mechanism at the neuromuscular junction , 2008, The Journal of cell biology.

[18]  George J Christ,et al.  The influence of electrospun aligned poly(epsilon-caprolactone)/collagen nanofiber meshes on the formation of self-aligned skeletal muscle myotubes. , 2008, Biomaterials.

[19]  Samir Mitragotri,et al.  Role of Particle Size in Phagocytosis of Polymeric Microspheres , 2008, Pharmaceutical Research.

[20]  Barry J. Arnow On Laplace's Extension of the Buffon Needle Problem , 1994 .

[21]  G. Whitesides,et al.  Unconventional Methods for Fabricating and Patterning Nanostructures. , 1999, Chemical reviews.

[22]  Shuichi Takayama,et al.  The effect of continuous wavy micropatterns on silicone substrates on the alignment of skeletal muscle myoblasts and myotubes. , 2006, Biomaterials.

[23]  P. Wigmore,et al.  The generation of fiber diversity during myogenesis. , 1998, The International journal of developmental biology.

[24]  D. Yaffe,et al.  Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle , 1977, Nature.

[25]  William P King,et al.  Myoblast alignment and differentiation on cell culture substrates with microscale topography and model chemistries. , 2007, Biomaterials.

[26]  P. Clark,et al.  Alignment of myoblasts on ultrafine gratings inhibits fusion in vitro. , 2002, The international journal of biochemistry & cell biology.

[27]  N. Gadegaard,et al.  The Effects of Collagen Type I Topography on Myoblasts In Vitro , 2004, Connective tissue research.

[28]  Terrance T. Kummer,et al.  Assembly of the postsynaptic membrane at the neuromuscular junction: paradigm lost , 2006, Current Opinion in Neurobiology.

[29]  G Cossu,et al.  Skeletal myogenesis on highly orientated microfibrous polyesterurethane scaffolds. , 2008, Journal of biomedical materials research. Part A.

[30]  Samir Mitragotri,et al.  Role of target geometry in phagocytosis. , 2006, Proceedings of the National Academy of Sciences of the United States of America.