Melt Electrowriting Allows Tailored Microstructural and Mechanical Design of Scaffolds to Advance Functional Human Myocardial Tissue Formation

材料科学 组织工程 肌节 诱导多能干细胞 脚手架 超细纤维 生物医学工程 心肌细胞 纤维 肌动蛋白 纳米技术 胚胎干细胞 生物物理学 复合材料 细胞 细胞生物学 细胞骨架 化学 生物 生物化学 基因 医学
作者
Miguel Castilho,Alain van Mil,Malachy Maher,Corina H.G. Metz,Gernot Hochleitner,Jürgen Gröll,Pieter A. Doevendans,Keita Ito,Joost P. G. Sluijter,Jos Malda
出处
期刊:Advanced Functional Materials [Wiley]
卷期号:28 (40) 被引量:208
标识
DOI:10.1002/adfm.201803151
摘要

Abstract Engineering native‐like myocardial muscle, recapitulating its fibrillar organization and mechanical behavior is still a challenge. This study reports the rational design and fabrication of ultrastretchable microfiber scaffolds with controlled hexagonal microstructures via melt electrowriting (MEW). The resulting structures exhibit large biaxial deformations, up to 40% strain, and an unprecedented compliance, delivering up to 40 times more elastic energy than rudimentary MEW fiber scaffolds. Importantly, when human induced pluripotent stem cell‐derived cardiomyocytes (iPSC‐CM) are encapsulated in a collagen‐based hydrogel and seeded on these microstructured and mechanically tailored fiber scaffolds, they show an increase in beating rate (1.5‐fold), enhanced cell alignment, sarcomere content and organization as well as an increase in cardiac maturation‐related marker expression (Cx43 1.8‐fold, cardiac Actin 1.5‐fold, SERCA2a 2.5‐fold, KCNJ2 1.5‐fold, and PPARGC1a 3.6‐fold), indicative of enhanced iPSC‐CM maturation, as compared to rudimentary fiber scaffolds. By combining these novel fiber scaffolds with clinically relevant human iPSC‐CMs, a heart patch that allows further maturation of contractile myocytes for cardiac tissue engineering is generated. Moreover, the designed scaffold allows successful shape recovery after epicardial delivery on a beating porcine heart, without negative effects on the engineered construct and iPSC‐CM viability.
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