平行定向诱导多能干细胞衍生神经元对排列肌纤维片组织收缩的控制。

Tissue Engineering Part A Pub Date : 2022-08-01 Epub Date: 2022-03-30 DOI:10.1089/ten.TEA.2021.0202
Hironobu Takahashi, Fumiko Oikawa, Naoya Takeda, Tatsuya Shimizu
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引用次数: 4

摘要

由不同类型细胞组成的工程复杂组织的制备和应用是组织工程下一阶段的重要里程碑。人体各组织成分的精细组织结构及其生理联系,使人体的一切功能得以实现。在这项研究中,基于细胞片的工程使我们能够利用来自人类诱导的多能干细胞的运动神经元来制造复杂的肌纤维片组织。与之前对其他群体的研究相比,我们利用条纹图案的热反应培养皿从人类成肌细胞中产生了具有仿生排列结构的肌纤维薄片,这使得通过简单地降低培养温度就可以操纵薄片组织。将肌纤维薄片转移到一种凝胶上,这种凝胶可以促进人体肌纤维的功能成熟,从而产生可收缩的人体肌肉组织。只要将运动神经元植入到薄片组织中,所有的神经元都与排列的肌纤维物理接触,并自主地与肌纤维方向平行伸长。此外,通过在肌纤维片上共培养,神经突外生物扩大。神经元的存在增强了肌纤维乙酰胆碱受体(achr)的聚集,通常在神经肌肉连接处(NMJs)发现。因此,肌纤维片的收缩行为是由神经元信号转导通过NMJs调节的。当谷氨酸刺激运动神经元时,肌肉收缩被诱导,并被作为AChR拮抗抑制剂的d-管curarine有效阻断。纤维蛋白基凝胶作为组织成熟的培养环境和通畅收缩的有利底物是有用的。我们的神经元-肌肉薄片组织将通过简单地扩大微图案基底和三维操作来扩展;制造厚组织和束状结构组织将可能仅仅通过多层或卷起薄片。简化控制自取向的神经突延伸将有利于制造这样一个大而复杂的组织。因此,我们在这项研究中建立的方法将有助于未来运动器械再生医学的应用。基于细胞片工程技术,从人体细胞中制备了包含骨骼肌纤维和诱导多能干细胞衍生的运动神经元的复杂组织。微图案热反应培养皿和基于纤维蛋白的凝胶底物能够产生排列一致且功能成熟的肌纤维片组织。运动神经元仅通过在排列好的肌纤维薄片组织上播种即可实现自主定向。肌肉收缩的诱导和抑制受神经元信号转导的有效控制。考虑到神经元-肌肉薄片组织的潜在可扩展性和可操作性,我们的方法将有助于未来运动器械再生医学的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contraction Control of Aligned Myofiber Sheet Tissue by Parallel Oriented Induced Pluripotent Stem Cell-Derived Neurons.

Fabrication and application of engineered complex tissues composed of different types of cells is a crucial milestone in the next phase of tissue engineering. The delicate organization structure of each tissue component and its physiological connections enable all the functions in the human body. In this study, cell sheet-based engineering allowed us to fabricate a complex myofiber sheet tissue using motor neurons derived from human-induced pluripotent stem cells. In contrast with previous studies of other groups, a myofiber sheet with a biomimetic aligned structure was produced from human myoblasts using a striped-patterned thermoresponsive dish, which enabled manipulation of the sheet tissue by simply lowering the culture temperature. The myofiber sheet was transferred onto a gel that promotes functional maturation of human myofibers, resulting in production of contractile human muscle tissue. Just by seeding motor neurons onto the sheet tissue, all the neurons physically contacted to the aligned myofibers, and autonomously elongated in parallel to the myofiber orientation. In addition, the neurite outgrowth was enlarged by coculturing on the myofiber sheet. The presence of the neurons enhanced clustering of myofiber acetylcholine receptors (AChRs), typically found at the neuromuscular junctions (NMJs). Consequently, contraction behaviors of the myofiber sheet were regulated by neuronal signal transduction through NMJs. Muscle contraction was induced when the motor neurons were stimulated by glutamic acid, and effectively blocked by administration of d-tubocurarine as an antagonistic inhibitor for the AChR. The fibrin-based gel was useful as a culture environment for tissue maturation and as a favorable substrate for unobstructed contractions. Our neuron-muscle sheet tissue will be scalable by simply enlarging the micropatterned substrate and manipulable three dimensionally; fabrication of a thick tissue and a bundle-like structured tissue will be possible just by layering multiple sheets or rolling up the sheet. Simplified control over self-orientation of neurite elongation will be advantageous for fabrication of such a large and complex tissue. Therefore, our methodology, established in this study, will be instrumental in future applications of regenerative medicine for locomotion apparatus. Impact Statement A complex tissue containing skeletal myofibers and induced pluripotent stem cell-derived motor neurons was fabricated from human cells based on the cell sheet engineering technology. A micropatterned thermoresponsive culture dish and a fibrin-based gel substrate enabled production of aligned, and functionally matured myofiber sheet tissue. The motor neurons were autonomously oriented simply by seeding on the aligned myofiber sheet tissue. Induction and inhibition of the muscle contraction were effectively controlled by neuronal signal transduction. Considering the potential scalability and manipulability of the neuron-muscle sheet tissue, our methodology will contribute to future applications of regenerative medicine for locomotion apparatus.

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Tissue Engineering Part A
Tissue Engineering Part A CELL & TISSUE ENGINEERING-BIOTECHNOLOGY & APPLIED MICROBIOLOGY
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