诱导多能干细胞
组织工程
细胞外基质
药物发现
计算机科学
计算生物学
可扩展性
人的心脏
神经科学
细胞生物学
生物医学工程
纳米技术
胚胎干细胞
生物
生物信息学
医学
材料科学
心脏病学
数据库
基因
生物化学
作者
Sang-Kyun Cho,Chelsea Lee,Mark A. Skylar‐Scott,Sarah C. Heilshorn,Joseph C. Wu
标识
DOI:10.1016/j.yjmcc.2021.04.006
摘要
Induced pluripotent stem cells (iPSCs) have emerged as a key component of cardiac tissue engineering, enabling studies of cardiovascular disease mechanisms, drug responses, and developmental processes in human 3D tissue models assembled from isogenic cells. Since the very first engineered heart tissues were introduced more than two decades ago, a wide array of iPSC-derived cardiac spheroids, organoids, and heart-on-a-chip models have been developed incorporating the latest available technologies and materials. In this review, we will first outline the fundamental biological building blocks required to form a functional unit of cardiac muscle, including iPSC-derived cells differentiated by soluble factors (e.g., small molecules), extracellular matrix scaffolds, and exogenous biophysical maturation cues. We will then summarize the different fabrication approaches and strategies employed to reconstruct the heart in vitro at varying scales and geometries. Finally, we will discuss how these platforms, with continued improvements in scalability and tissue maturity, can contribute to both basic cardiovascular research and clinical applications in the future.
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