Development and application of 3D cardiac tissues derived from human pluripotent stem cells

IF 2.2 4区 医学 Q2 PHARMACOLOGY & PHARMACY Drug Metabolism and Pharmacokinetics Pub Date : 2025-02-01 DOI:10.1016/j.dmpk.2024.101049
Masatoshi Ohno , Hidenori Tani , Shugo Tohyama
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Abstract

Recently human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) have become an attractive platform to evaluate drug responses for cardiotoxicity testing and disease modeling. Moreover, three-dimensional (3D) cardiac models, such as engineered heart tissues (EHTs) developed by bioengineering approaches, and cardiac spheroids (CSs) formed by spherical aggregation of hPSC-CMs, have been established as useful tools for drug discovery and transplantation. These 3D models overcome many of the shortcomings of conventional 2D hPSC-CMs, such as immaturity of the cells. Cardiac organoids (COs), like other organs, have also been studied to reproduce structures that resemble a heart in vivo more closely and optimize various culture conditions. Heart-on-a-chip (HoC) developed by a microfluidic chip-based technology that enables real-time monitoring of contraction and electrical activity, provides multifaceted information that is essential for capturing natural tissue development in vivo. Recently, 3D experimental systems have been developed to study organ interactions in vitro. This review aims to discuss the developments and advancements of hPSC-CMs and 3D cardiac tissues.
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人类多能干细胞衍生的三维心脏组织的开发与应用。
最近,人类多能干细胞来源的心肌细胞(hPSC-CMs)已成为评估药物反应的一个有吸引力的平台,用于心脏毒性测试和疾病建模。此外,三维(3D)心脏模型,如通过生物工程方法开发的工程化心脏组织(EHTs),以及由hPSC-CMs的球形聚集形成的心脏球体(CSs),已被建立为药物发现和移植的有用工具。这些3D模型克服了传统2D hPSC-CMs的许多缺点,例如细胞不成熟。与其他器官一样,心脏类器官(COs)也被研究在体内更接近地复制类似心脏的结构,并优化各种培养条件。芯片上的心脏(HoC)由一种基于微流控芯片的技术开发,能够实时监测收缩和电活动,为捕获体内自然组织发育提供必要的多方面信息。最近,三维实验系统已经发展到体外研究器官相互作用。本文就hPSC-CMs和三维心脏组织的研究进展进行综述。
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来源期刊
CiteScore
4.80
自引率
9.50%
发文量
50
审稿时长
69 days
期刊介绍: DMPK publishes original and innovative scientific papers that address topics broadly related to xenobiotics. The term xenobiotic includes medicinal as well as environmental and agricultural chemicals and macromolecules. The journal is organized into sections as follows: - Drug metabolism / Biotransformation - Pharmacokinetics and pharmacodynamics - Toxicokinetics and toxicodynamics - Drug-drug interaction / Drug-food interaction - Mechanism of drug absorption and disposition (including transporter) - Drug delivery system - Clinical pharmacy and pharmacology - Analytical method - Factors affecting drug metabolism and transport - Expression of genes for drug-metabolizing enzymes and transporters - Pharmacogenetics and pharmacogenomics - Pharmacoepidemiology.
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