Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts, USA.
Biophys J. 2009 Nov 18;97(10):2771-9. doi: 10.1016/j.bpj.2009.08.038.
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.
通过软光刻技术制造的微图案聚二甲基硅氧烷(PDMS)基底导致培养中的成肌细胞大规模定向排列,从而控制它们形成的肌管的方向。在许多化学性质相同的表面上,融合发生在排列成正方形或六边形晶格的不同结构中,但只有一部分图案化表面产生了对齐的肌管。值得注意的是,在一些基底上,大量的肌管以可重复的锐角取向于图案化特征的晶格。一个简单的几何模型可以根据最大化成肌细胞与图案化形貌表面之间的接触面积来预测角度和取向程度。微图案化基底还提供了短期线索,影响了更高阶的功能,如粘着斑的定位和突触后乙酰胆碱受体的积累。我们的结果代表了我们认为是一种新的肌肉骨骼组织工程方法,我们的模型揭示了体内肌管定向的机制。