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用于研究心肌缺血再灌注损伤的多细胞3D模型。

Multicellular 3D models to study myocardial ischemia-reperfusion injury.

作者信息

Peletier Merel, Zhang Xiaohan, Klein Scarlett, Kroon Jeffrey

机构信息

Department of Experimental Vascular Medicine, Amsterdam Cardiovascular Sciences, Amsterdam UMC Location University of Amsterdam, Amsterdam, Netherlands.

Amsterdam Cardiovascular Sciences, Atherosclerosis and Ischemic Syndromes, Amsterdam, Netherlands.

出版信息

Front Cell Dev Biol. 2024 Nov 15;12:1494911. doi: 10.3389/fcell.2024.1494911. eCollection 2024.

Abstract

Coronary heart disease is a major global health threat, with acute myocardial ischemia-reperfusion injury (IRI) being a major contributor to myocardial damage following an ischemic event. IRI occurs when blood flow to ischemic tissues is restored and exacerbates the cellular damage caused by ischemia/hypoxia. Although animal studies investigating IRI have provided valuable insights, their translation into clinical outcomes has been limited, and translation into medical practice remains cumbersome. Recent advancements in engineered three-dimensional human models could offer a promising avenue to bridge the "therapeutic valley of death" from bench to bedside, enhancing the understanding of IRI pathology. This review summarizes the current state-of-the-art cardiovascular 3D models, including spheroids, organoids, engineered cardiac microtissues, and organ-on-a-chip systems. We provide an overview of their advantages and limitations in the context of IRI, with a particular emphasis on the crucial roles of cell-cell communication and the multi-omics approaches to enhance our understanding of the pathophysiological processes involved in IRI and its treatment. Finally, we discuss currently available multicellular human 3D models of IRI.

摘要

冠心病是全球主要的健康威胁,急性心肌缺血再灌注损伤(IRI)是缺血事件后心肌损伤的主要原因。当缺血组织的血流恢复时,就会发生IRI,这会加剧缺血/缺氧所造成的细胞损伤。尽管对IRI进行研究的动物实验提供了有价值的见解,但将这些见解转化为临床结果仍然有限,而且转化为医学实践也很麻烦。工程化三维人体模型的最新进展可能为弥合从实验台到病床的“治疗死亡谷”提供一条有前景的途径,增进对IRI病理的理解。本综述总结了当前最先进的心血管三维模型,包括球体、类器官、工程化心脏微组织和芯片器官系统。我们概述了它们在IRI背景下的优点和局限性,特别强调细胞间通讯的关键作用以及多组学方法,以增进我们对IRI及其治疗所涉及的病理生理过程的理解。最后,我们讨论了目前可用的IRI多细胞人体三维模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57a2/11606089/150c49e28aa0/fcell-12-1494911-g001.jpg

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