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用于遗传性和后天性心脏病体外建模的生物工程方法。

Bioengineering Approaches to In Vitro Modeling of Genetic and Acquired Cardiac Diseases.

作者信息

Jin Linqi, Hwang Boeun, Rezapourdamanab Sarah, Sridhar Vani, Nandwani Roshni, Amoli Mehdi Salar, Serpooshan Vahid

机构信息

Department of Biomedical Engineering, Emory University School of Medicine and Georgia Institute of Technology, Atlanta, GA, 30322, USA.

Department of Biology, Emory University, Atlanta, GA, 30322, USA.

出版信息

Curr Cardiol Rep. 2025 Mar 20;27(1):72. doi: 10.1007/s11886-025-02218-7.

Abstract

PURPOSE OF REVIEW

This review aims to explore recent advancements in bioengineering approaches used in developing and testing in vitro cardiac disease models. It seeks to find out how these tools can address the limitations of traditional in vitro models and be applied to improve our understanding of cardiac disease mechanisms, facilitate preclinical drug screening, and equip the development of personalized therapeutics.

RECENT FINDINGS

Human induced pluripotent stem cells have enabled the generation of diverse cardiac cell types and patient-specific models. Techniques like 3D tissue engineering, heart-on-a-chip platforms, biomechanical conditioning, and CRISPR-based gene editing have enabled faithful recreation of complex cardiac microenvironments and disease conditions. These models have advanced the study of both genetic and acquired cardiac disorders. Bioengineered in vitro models are transforming the basic science and clinical research in cardiovascular disease by improving the biomimicry and complexity of tissue analogues, increasing throughput and reproducibility of screening platforms, as well as offering patient and disease specificity. Despite challenges in scalability and functional maturity, integrating multiple bioengineering techniques with advanced analytical tools in in vitro modeling platforms holds promise for future precision and personalized medicine and therapeutic innovations.

摘要

综述目的

本综述旨在探讨用于开发和测试体外心脏病模型的生物工程方法的最新进展。旨在了解这些工具如何克服传统体外模型的局限性,并应用于增进我们对心脏病机制的理解、促进临床前药物筛选以及推动个性化治疗的发展。

最新发现

人类诱导多能干细胞已能够生成多种心脏细胞类型和患者特异性模型。三维组织工程、芯片上心脏平台、生物力学调节以及基于CRISPR的基因编辑等技术,已能够逼真地重现复杂的心脏微环境和疾病状况。这些模型推动了对遗传性和后天性心脏病的研究。生物工程体外模型正在通过提高组织类似物的仿生学和复杂性、增加筛选平台的通量和可重复性以及提供患者和疾病特异性,来改变心血管疾病的基础科学和临床研究。尽管在可扩展性和功能成熟度方面存在挑战,但在体外建模平台中将多种生物工程技术与先进分析工具相结合,有望实现未来的精准和个性化医学以及治疗创新。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20c/11926001/cc8d11029784/11886_2025_2218_Fig1_HTML.jpg

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