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Tissue-engineered 3-dimensional (3D) microenvironment enhances the direct reprogramming of fibroblasts into cardiomyocytes by microRNAs

机译:组织工程3维(3D)微环境可增强通过microRNA将成纤维细胞直接重编程为心肌细胞

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摘要

We have recently shown that a combination of microRNAs, miR combo, can directly reprogram cardiac fibroblasts into functional cardiomyocytes in vitro and in vivo. Reprogramming of cardiac fibroblasts by miR combo in vivo is associated with improved cardiac function following myocardial infarction. However, the efficiency of direct reprogramming in vitro is relatively modest and new strategies beyond the traditional two-dimensional (2D) culture should be identified to improve reprogramming process. Here, we report that a tissue-engineered three-dimensional (3D) hydrogel environment enhanced miR combo reprogramming of neonatal cardiac and tail-tip fibroblasts. This was associated with significantly increased MMPs expression in 3D vs. 2D cultured cells, while pharmacological inhibition of MMPs blocked the effect of the 3D culture on enhanced miR combo mediated reprogramming. We conclude that 3D tissue-engineered environment can enhance the direct reprogramming of fibroblasts to cardiomyocytes via a MMP-dependent mechanism.
机译:我们最近显示,miR组合的microRNA组合可以在体外和体内将心脏成纤维细胞直接重编程为功能性心肌细胞。体内miR组合对心脏成纤维细胞进行重编程与心肌梗死后心脏功能的改善有关。但是,在体外直接重编程的效率相对较低,应该确定超越传统二维(2D)文化的新策略来改善重编程过程。在这里,我们报告组织工程三维(3D)水凝胶环境增强了新生儿心脏和尾尖成纤维细胞的miR组合重编程。这与3D和2D培养细胞中MMPs表达的显着增加有关,而MMPs的药理学抑制作用阻止了3D培养物对增强的miR组合介导的重编程的影响。我们得出的结论是3D组织工程化的环境可以通过MMP依赖性机制增强成纤维细胞向心肌细胞的直接重编程。

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