Cardiac Inducing RNAs (CIRs) from Human Fetal Heart Promote the Differentiation of Non-Muscle Cells to Form into Cardiomyocytes in vitro

L. Lemanski
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Abstract

We have discovered a cardiac-inducing RNA (CIR) in the axolotl, Ambystoma mexicanum , (a salamander) and two cardiac inducing RNAs (CIR-6 and CIR-30) in human heart that have the ability to induce the differentiation of non-muscle cells, including induced pluripotent stem cells from human skin, mouse embryonic stem cells, and mouse fibroblasts into cardiomyocytes in vitro . Although the primary sequences of salamander and human RNAs are not homologous, their secondary structures are very similar and we believe account for their shared unique abilities to promote differentiation of non-muscle cells into definitive cardiomyocytes. We are beginning to explore the potential for repair/regeneration of cardiac muscle in vivo using mouse and rat models with induced acute myocardial infarctions (AMI) to determine if pluripotent stem cells or fibroblasts transfected with the human CIRs or CIRs alone injected into the damaged areas of the hearts can affect repair of the damaged cardiac muscle tissue and return the infarcted hearts and the AMI animal models to pre-heart-attack function again. If cardiac cells damaged in heart attacks can be replaced with living, functioning cardiomyocytes, patients with heart disease would be able to have normal heart function restored and could return to normal pre-heart-attack activity levels. Understanding how CIR transforms non-muscle cells into vigorously contracting, functional cardiac muscle and effectively replacing damaged heart cells with newly-formed cardiac muscle tissue would represent a major breakthrough in modern biology and medicine with the potential to have a significant impact on the survival rate and quality of life of millions of individuals worldwide who suffer heart attacks each year.
心脏诱导rna (CIRs)在体外促进非肌肉细胞向心肌细胞的分化
我们在蝾螈,Ambystoma mexicanum(一种蝾螈)和人类心脏中发现了一种心脏诱导RNA (CIR)和两种心脏诱导RNA (CIR-6和CIR-30),它们具有诱导非肌肉细胞分化的能力,包括来自人类皮肤的诱导多能干细胞、小鼠胚胎干细胞和小鼠成纤维细胞在体外分化为心肌细胞。虽然蝾螈和人类rna的一级序列不同源,但它们的二级结构非常相似,我们相信这是它们共同的独特能力,可以促进非肌肉细胞分化为最终的心肌细胞。我们正开始探索体内心肌修复/再生的潜力,使用小鼠和大鼠模型诱导急性心肌梗死(AMI),以确定多能干细胞或成纤维细胞转染人CIRs或单独注射到心脏受损区域,是否可以影响受损心肌组织的修复,并使梗死心脏和AMI动物模型再次恢复到心脏病发作前的功能。如果在心脏病发作中受损的心脏细胞可以被活的、功能正常的心肌细胞所取代,心脏病患者将能够恢复正常的心脏功能,并恢复到心脏病发作前的正常活动水平。了解CIR如何将非肌肉细胞转化为有力收缩的功能性心肌,并有效地将受损的心脏细胞替换为新形成的心肌组织,将是现代生物学和医学的重大突破,有可能对全球每年数百万心脏病患者的存活率和生活质量产生重大影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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