利用人源性心脏诱导RNA (CIR)诱导小鼠胚胎成纤维细胞向心肌细胞分化

L. Lemanski, A. Kochegarov, K. Kaveh, Michael Neal, A. Arms, Yelica L Rodriguez, Lan Hong, M. J. Equbal, Pipasha Biswas, Priya Biswas, M. Gonzalez, Jewel Ross-Ferguson, Justin Rusk, Lani Lyman- Henley, Tearah McRae-Kee, Curtis Ivory, Zhengshan Zhao
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引用次数: 1

摘要

本研究探索了我们在人类心脏中发现的一种RNA,该RNA在体外诱导小鼠胚胎干细胞和人诱导多能干细胞分化为心肌细胞。我们将这种RNA命名为心脏诱导RNA或CIR,我们现在发现CIR也能诱导小鼠胚胎成纤维细胞(MEF)在体外形成心肌细胞。在这些研究中,使用脂质体将人源性CIR转染到MEF中。转染了cirr的小鼠成纤维细胞呈现梭形细胞,这是培养心肌细胞的特征,并表达心肌特异性肌钙蛋白-t和心肌原肌球蛋白。因此,在体外,cirr诱导的成纤维细胞向心肌细胞的转化似乎没有初始去分化为多能干细胞。相反,在使用脂质体转染系统转染CIR后,在接下来的8天内,培养的成纤维细胞˃80%似乎直接转分化为最终的心肌细胞。在使用非活性RNA或脂质胺的对照组中,只有不到Ë 7%的人表现出心肌细胞特征。因此,CIR的发现可能具有重大的潜力,用于心肌梗死或其他疾病过程后人类受损心肌组织的修复/再生,使受影响的患者能够恢复到心脏病前的活动水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differentiation of Mouse Embryonic Fibroblasts (MEFs) into Cardiomyocytes Using Human-Derived Cardiac Inducing RNA (CIR)
The present study explores an RNA we have discovered in human heart that induces differentiation of mouse embryonic stem cells and human induced pluripotent stem cells into cardiomyocytes in vitro. We have designated this RNA as Cardiac Inducing RNA or CIR. We now find that CIR also induces mouse embryonic fibroblasts (MEF) to form cardiomyocytes in vitro. For these studies, human-derived CIR is transfected into MEF using lipofectamine. The CIR-transfected mouse fibroblasts exhibit spindle-shaped cells, characteristic of myocardial cells in culture and express cardiac-specific troponin-T and cardiac tropomyosin. As such, the CIR-induced conversion of the fibroblasts into cardiomyocytes in vitro appears to take place without initial dedifferentiation into pluripotent stem cells. Instead, after CIR transfection using a lipofectamine transfection system, over the next 8 days there appears to be a direct transdifferentiation of ˃80% of the cultured fibroblasts into definitive cardiomyocytes. Fewer than ˂7% of the untreated controls using non-active RNA or lipofectamine by itself show cardiomyocyte characteristics. Thus, discovery of CIR may hold significant potential for future use in repair/regeneration of damaged myocardial tissue in humans after myocardial infarction or other disease processes such that affected patients may be able to return to pre-heart-disease activity levels.
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