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利用桥粒蛋白 2 突变肌原纤维构建致心律失常性心肌病的工程心脏切片模型。

Engineered Heart Slice Model of Arrhythmogenic Cardiomyopathy Using Plakophilin-2 Mutant Myocytes.

机构信息

Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland.

出版信息

Tissue Eng Part A. 2019 May;25(9-10):725-735. doi: 10.1089/ten.TEA.2018.0272. Epub 2019 Feb 15.

Abstract

Genetic heart diseases such as arrhythmogenic cardiomyopathy (AC), a common genetic cause of sudden cardiac death, can be modeled using patient-specific induced pluripotent stem cell-derived cardiac myocytes (CMs). However, it is important to culture these cells in a multicellular syncytium with exposure to surrounding matrix cues to create more accurate and robust models of the disease due to the importance of cell-cell and cell-matrix interactions. The engineered heart slice, constructed by seeding CMs on intact decellularized matrix slices, allows molecular and functional studies on an aligned multilayered syncytium of CMs. This study reveals the potential for an improved disease-in-a-dish model of AC.

摘要

遗传性心脏病,如心律失常性心肌病(AC),是一种常见的导致心源性猝死的遗传病因,可以通过使用患者特异性诱导多能干细胞衍生的心肌细胞(CM)来建模。然而,由于细胞-细胞和细胞-基质相互作用的重要性,将这些细胞培养在具有周围基质线索的多核合胞体中对于创建更准确和强大的疾病模型非常重要。工程心脏切片通过将 CM 接种在完整的去细胞化基质切片上构建,允许对 CM 的对齐多层合胞体进行分子和功能研究。这项研究揭示了改善 AC 疾病在体外模型的潜力。

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