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用于模拟心脏发育和药物筛选的工程平台。

Engineered platforms for mimicking cardiac development and drug screening.

作者信息

Stiefbold Madison, Zhang Haokang, Wan Leo Q

机构信息

Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Biotech 2147, 110 8t Street, Troy, NY, 12180, USA.

Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, NY, 12180, USA.

出版信息

Cell Mol Life Sci. 2024 Apr 25;81(1):197. doi: 10.1007/s00018-024-05231-1.

Abstract

Congenital heart defects are associated with significant health challenges, demanding a deep understanding of the underlying biological mechanisms and, thus, better devices or platforms that can recapitulate human cardiac development. The discovery of human pluripotent stem cells has substantially reduced the dependence on animal models. Recent advances in stem cell biology, genetic editing, omics, microfluidics, and sensor technologies have further enabled remarkable progress in the development of in vitro platforms with increased fidelity and efficiency. In this review, we provide an overview of advancements in in vitro cardiac development platforms, with a particular focus on technological innovation. We categorize these platforms into four areas: two-dimensional solid substrate cultures, engineered substrate architectures that enhance cellular functions, cardiac organoids, and embryos/explants-on-chip models. We conclude by addressing current limitations and presenting future perspectives.

摘要

先天性心脏缺陷与重大的健康挑战相关,这需要深入了解其潜在的生物学机制,进而需要更好的能够模拟人类心脏发育的装置或平台。人类多能干细胞的发现大幅减少了对动物模型的依赖。干细胞生物学、基因编辑、组学、微流体和传感器技术的最新进展进一步推动了体外平台的发展,使其具有更高的保真度和效率。在本综述中,我们概述了体外心脏发育平台的进展,特别关注技术创新。我们将这些平台分为四个领域:二维固体基质培养、增强细胞功能的工程化基质结构、心脏类器官以及芯片上的胚胎/外植体模型。我们通过讨论当前的局限性并展望未来前景来结束本文。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f2f/11073210/55b1b22be27f/18_2024_5231_Fig1_HTML.jpg

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