WPI-Advanced Institute for Materials Research, Tohoku University, Sendai, Japan.
California NanoSystems Institute (CNSI), and Center for Minimally Invasive Therapeutics (C-MIT), Department of Bioengineering and Department of Radiology, University of California, Los Angeles, California.
J Tissue Eng Regen Med. 2018 Nov;12(11):2151-2163. doi: 10.1002/term.2738. Epub 2018 Sep 30.
Bioengineered functional muscle tissues are beneficial for regenerative medicine due to their treatment potential for various debilitating disorders, including myopathy and traumatic injuries. However, the contractile properties of engineered muscle constructs are lacking compared with their native counterparts. Here, we used microfluidic spinning to fabricate photocrosslinkable gelatin methacryloyl (GelMA) hydrogel fibres with well-defined surface morphologies for engineering muscle tissues. We examined whether the combination of topographical cues from surface micropatterning and biochemical stimulation with recombinant agrin can improve the generation of bioengineered muscle tissue. Topographical cues on micropatterned fibres promoted alignment of C2C12 myoblasts and augmented myotube formation during differentiation, as assessed by increased myotube length, aspect ratio, and the elevated mRNA expression of myogenic genes. Moreover, agrin treatment significantly increased acetylcholine receptor expression/clustering and myotube formation and upregulated dystrophin expression in differentiated C2C12 myotubes. Interestingly, the combination of topographical cues with agrin treatment further enhanced myotube maturation and functionality as shown by improved contractility under electrical stimulation. Thus, combining topographical cues and agrin treatment improved functions of engineered muscle tissue, which has potential in biorobotics, drug screening, tissue engineering, and regenerative medicine.
生物工程功能性肌肉组织因其在各种衰弱性疾病(包括肌病和创伤性损伤)中的治疗潜力,而有益于再生医学。然而,与天然肌肉组织相比,工程化肌肉构建物的收缩性能较差。在这里,我们使用微流控纺丝技术制造了具有明确定义的表面形态的光交联明胶甲基丙烯酰(GelMA)水凝胶纤维,用于工程化肌肉组织。我们研究了表面微图案化的形貌线索与重组聚集蛋白的生化刺激相结合是否可以改善生物工程肌肉组织的生成。微图案化纤维上的形貌线索促进了 C2C12 成肌细胞的对齐,并在分化过程中增加了肌管的形成,这可以通过增加肌管的长度、长宽比以及肌生成基因的 mRNA 表达来评估。此外,聚集蛋白处理显著增加了乙酰胆碱受体的表达/聚集和肌管的形成,并上调了分化的 C2C12 肌管中的肌营养不良蛋白的表达。有趣的是,形貌线索与聚集蛋白处理的结合进一步增强了肌管的成熟和功能,表现为在电刺激下改善了收缩性。因此,结合形貌线索和聚集蛋白处理可以改善工程化肌肉组织的功能,这在生物机器人、药物筛选、组织工程和再生医学方面具有潜力。