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利用蛋白质转导短暂激活重编程转录因子有助于将人成纤维细胞转化为类心肌细胞。

Transient Activation of Reprogramming Transcription Factors Using Protein Transduction Facilitates Conversion of Human Fibroblasts Toward Cardiomyocyte-Like Cells.

作者信息

Ghazizadeh Zaniar, Rassouli Hassan, Fonoudi Hananeh, Alikhani Mehdi, Talkhabi Mahmood, Darbandi-Azar Amir, Chen Shuibing, Baharvand Hossein, Aghdami Nasser, Salekdeh Ghasem Hosseini

机构信息

Department of Stem Cells and Developmental Biology at Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.

School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Mol Biotechnol. 2017 Jun;59(6):207-220. doi: 10.1007/s12033-017-0007-x.

Abstract

Derivation of cardiomyocytes directly from patients' own fibroblasts could offer a new therapeutic approach for those with ischemic heart disease. An essential step toward clinical application is to establish safe conversion of human fibroblasts into a cardiac fate. Here we aimed to efficiently and safely generate cardiomyocytes from human fibroblasts by direct delivery of reprogramming recombinant cell permeant form of reprogramming proteins followed by cardio-inductive signals. Human fetal and adult fibroblasts were transiently exposed to transactivator of transcription-fused recombinant OCT4, SOX2, KLF4 and c-MYC for 2 weeks and then were directly differentiated toward protein-induced cardiomyocyte-like cells (p-iCLCs) in a cardiac fate niche, carried out by treatment with a set of cardiogenic small molecules (sequential treatment of Chir, and IWP-2, SB431542 and purmorphamine). The cells showed cardiac phenotype over a period of 3 weeks without first undergoing reprogramming into or through a pluripotent intermediate, shown by lack of expression of key pluripotency markers. p-iCLCs exhibited cardiac features at both the gene and protein levels. Our study provides an alternative method for the generation of p-iCLCs which shortcut reprogramming toward allogeneic cardiomyocytes in a safe and efficient manner and could facilitate generation of genetic material-free cardiomyocytes.

摘要

直接从患者自身的成纤维细胞中获得心肌细胞,可能为患有缺血性心脏病的患者提供一种新的治疗方法。临床应用的一个关键步骤是建立将人类成纤维细胞安全转化为心脏细胞命运的方法。在这里,我们旨在通过直接递送重编程蛋白的重组细胞穿透形式,随后给予心脏诱导信号,从人类成纤维细胞中高效、安全地生成心肌细胞。人类胎儿和成体成纤维细胞短暂暴露于与转录激活因子融合的重组OCT4、SOX2、KLF4和c-MYC中2周,然后在心脏细胞命运微环境中直接分化为蛋白诱导的心肌样细胞(p-iCLCs),这是通过用一组心脏发生小分子(依次使用Chir、IWP-2、SB431542和嘌呤胺处理)来实现的。这些细胞在3周内表现出心脏表型,而无需首先重编程为多能中间状态或通过多能中间状态,这通过关键多能性标记物的缺乏表达得以证明。p-iCLCs在基因和蛋白质水平上均表现出心脏特征。我们的研究提供了一种生成p-iCLCs的替代方法,该方法以安全、高效的方式绕过重编程生成同种异体心肌细胞,并可能促进无遗传物质心肌细胞的生成。

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