Department of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts.
J Biomed Mater Res B Appl Biomater. 2020 Jul;108(5):2308-2319. doi: 10.1002/jbm.b.34566. Epub 2020 Jan 22.
To regenerate functional muscle tissue, engineered scaffolds should impart topographical features to induce myoblast alignment by a phenomenon known as contact guidance. Myoblast alignment is an essential step towards myotube formation, which is guided in vivo by extracellular matrix structure and micron-scale grooves between adjacent muscle fibers. Fibrin microthread scaffolds mimic the morphological architecture of native muscle tissue and have demonstrated promise as an implantable scaffold for treating skeletal muscle injuries. While these scaffolds promote modest myoblast alignment, it is not sufficient to generate highly functional muscle tissue. The goal of this study is to develop and characterize a new method of etching the surface of fibrin microthreads to incorporate aligned, sub-micron grooves that promote myoblast alignment. To generate these topographic features, we placed fibrin microthreads into 2-(N-morpholino)ethane-sulfonic acid (MES) acidic buffer and evaluated the effect of buffer pH on the generation of these features. Surface characterization with atomic force microscopy and scanning electron microscopy indicated the generation of aligned, sub-micron sized grooves on microthreads in MES buffer with pH 5.0. Microthreads etched with surface features had tensile mechanical properties comparable to controls, indicating that the surface treatment does not inhibit scaffold bulk properties. Our data demonstrate that etching threads in MES buffer with pH 5.0 enhanced alignment and filamentous actin stress fiber organization of myoblasts on the surface of scaffolds. The ability to tune topographic features on the surfaces of scaffolds independent of mechanical properties provides a valuable tool for designing microthread-based scaffolds to enhance regeneration of functional muscle tissue.
为了再生功能性肌肉组织,工程支架应赋予拓扑特征,通过一种称为接触引导的现象来诱导成肌细胞排列。成肌细胞排列是肌管形成的关键步骤,肌管在体内受到细胞外基质结构和相邻肌肉纤维之间的微米级凹槽的引导。纤维蛋白微丝支架模拟天然肌肉组织的形态结构,已被证明是一种有前途的可植入支架,可用于治疗骨骼肌损伤。虽然这些支架促进了适度的成肌细胞排列,但不足以产生高度功能性的肌肉组织。本研究的目的是开发和表征一种新的纤维蛋白微丝表面蚀刻方法,以纳入排列整齐的亚微米级凹槽,促进成肌细胞排列。为了产生这些形貌特征,我们将纤维蛋白微丝放入 2-(N-吗啉)乙磺酸(MES)酸性缓冲液中,并评估缓冲液 pH 值对这些特征产生的影响。原子力显微镜和扫描电子显微镜的表面特性表明,在 pH 值为 5.0 的 MES 缓冲液中,微丝上会产生排列整齐的亚微米大小的凹槽。用表面特征蚀刻的微丝具有与对照相当的拉伸力学性能,表明表面处理不会抑制支架的整体性质。我们的数据表明,用 pH 值为 5.0 的 MES 缓冲液蚀刻微丝可增强成肌细胞在支架表面的排列和丝状肌动蛋白应力纤维组织。能够独立于机械性能在支架表面上调整形貌特征为设计基于微丝的支架以增强功能性肌肉组织再生提供了有价值的工具。