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利用微小RNA将心脏成纤维细胞直接重编程为心肌细胞。

Direct reprogramming of cardiac fibroblasts to cardiomyocytes using microRNAs.

作者信息

Jayawardena Tilanthi, Mirotsou Maria, Dzau Victor J

机构信息

Division of Cardiology, Department of Medicine, Mandel Center for Hypertension and Atherosclerosis Research, and the Cardiovascular Research Center, Duke University Medical Center, DUMC Box 3701, Durham, NC, 27710, USA.

出版信息

Methods Mol Biol. 2014;1150:263-72. doi: 10.1007/978-1-4939-0512-6_18.

Abstract

The therapeutic administration of microRNAs represents an innovative reprogramming strategy with which to advance cardiac regeneration and personalized medicine. Recently, a distinct set of microRNAs was found capable of converting murine fibroblasts to cardiomyocyte-like cells in vitro. Further treatment with JAK inhibitor I significantly enhanced the efficiency of the microRNA-mediated reprogramming (Jayawardena et al., Circ Res 110(11):1465-1473, 2012). This novel technique serves as an initial tool for switching the cell fate of cardiac fibroblasts toward the cardiomyocyte lineage using microRNAs. As the budding field of reprogramming biology develops, we hope that a thorough examination of the chemical, physical, and temporal parameters determining reprogramming efficiency and maturation will enable a better understanding of the mechanisms governing cardiac cell fate and provide new approaches for drug discovery and therapy for cardiovascular diseases.

摘要

微小RNA的治疗性给药代表了一种创新的重编程策略,可用于推动心脏再生和个性化医疗。最近,发现了一组独特的微小RNA能够在体外将小鼠成纤维细胞转化为心肌样细胞。用JAK抑制剂I进一步处理可显著提高微小RNA介导的重编程效率(Jayawardena等人,《循环研究》110(11):1465 - 1473,2012年)。这项新技术作为一种初始工具,可利用微小RNA将心脏成纤维细胞的细胞命运转向心肌细胞谱系。随着重编程生物学这一新兴领域的发展,我们希望对决定重编程效率和成熟度的化学、物理和时间参数进行全面研究,能够更好地理解控制心脏细胞命运的机制,并为心血管疾病的药物发现和治疗提供新方法。

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