首页> 外文期刊>Stem cells translational medicine. >Bioengineered Myocardium Derived from Induced Pluripotent Stem Cells Improves Cardiac Function and Attenuates Cardiac Remodeling Following Chronic Myocardial Infarction in Rats
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Bioengineered Myocardium Derived from Induced Pluripotent Stem Cells Improves Cardiac Function and Attenuates Cardiac Remodeling Following Chronic Myocardial Infarction in Rats

机译:诱导多能干细胞衍生的生物工程心肌改善大鼠慢性心肌梗死后的心脏功能并减轻其心脏重塑

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Cell-based therapies are promising strategies for myocardial repair following myocardial infarction. Induced pluripotent stem (iPS) cells have the potential to generate many cardiomyocytes, and they hold significant promise for the application of regenerative medicine to heart failure. Here, we developed cardiac tissue sheets, termed bioengineered myocardium (BM), from mouse iPS cells and measured cardiac performance following BM implantation in a rat chronic myocardial infarction model. Immunostaining analyses revealed that the -actinin+ cell population was isolated with more than 99% purity under specific culture conditions. To evaluate the contribution of BM to the improvements in cardiac performance, we induced myocardial infarction in 30 F344/NJcl-rnu/rnu rats by left anterior descending coronary ligation. The rats were randomly divided into two groups, 2 weeks after ligation: a BM implantation group (n = 15) and a sham group (n = 15). Echocardiography and catheter examination showed that the BM implantation significantly improved cardiac function and attenuated cardiac remodeling compared with the sham group. Histological analyses demonstrated that the implanted BM survived at the epicardial implantation site 4 weeks after implantation. The implanted BM survived and attenuated left ventricular remodeling in the rat chronic myocardial infarction model. Thus, BM derived from iPS cells might be a promising new treatment for heart failure.
机译:基于细胞的疗法是心肌梗死后心肌修复的有前途的策略。诱导多能干(iPS)细胞具有产生许多心肌细胞的潜力,它们对于将再生医学应用于心力衰竭具有重要的前景。在这里,我们从小鼠iPS细胞开发了称为生物工程心肌(BM)的心脏组织表,并在大鼠慢性心肌梗死模型中测量了BM植入后的心脏性能。免疫染色分析表明,在特定的培养条件下,分离出的-actinin +细胞群纯度超过99%。为了评估BM对改善心脏功能的贡献,我们通过左前降支结扎术在30只F344 / NJcl-rnu / rnu大鼠中诱发了心肌梗塞。结扎后2周,将大鼠随机分为两组:BM植入组(n = 15)和假手术组(n = 15)。超声心动图和导管检查显示,与假手术组相比,BM植入显着改善了心脏功能,并减弱了心脏重塑。组织学分析表明,植入的BM在植入后4周在心外膜植入部位存活。在大鼠慢性心肌梗死模型中,植入的BM存活并减弱了左心室重塑。因此,源自iPS细胞的BM可能是一种有前途的心力衰竭新疗法。

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