首页> 外文期刊>Journal of the American College of Cardiology >Pre-treatment of mesenchymal stem cells with a combination of growth factors enhances gap junction formation, cytoprotective effect on cardiomyocytes, and therapeutic efficacy for myocardial infarction.
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Pre-treatment of mesenchymal stem cells with a combination of growth factors enhances gap junction formation, cytoprotective effect on cardiomyocytes, and therapeutic efficacy for myocardial infarction.

机译:用生长因子组合预处理间充质干细胞可增强间隙连接的形成,对心肌细胞的细胞保护作用以及对心肌梗塞的治疗功效。

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摘要

OBJECTIVES: The goal of this study was to investigate the effect of pre-treatment of mesenchymal stem cells (MSCs) with growth factors (GFs) on cardiomyogenic differentiation, cytoprotective action on cardiomyocytes (CMCs), and their therapeutic efficacy in myocardial infarction. BACKGROUND: Mechanisms of myocardial repair with MSC transplantation have not been fully elucidated, and therapeutic efficacy needs to be enhanced. METHODS: The MSCs obtained from the bone marrow of Fisher344 rats were treated with fibroblast growth factor-2, insulin-like growth factor-1, and bone morphogenetic protein-2. The expression of cardiac specific markers and the cytoprotective effect of MSCs with its mechanism were evaluated. Efficacy of MSCs transplantation was studied in rat myocardial infarction model. RESULTS: Treatment of MSCs with cocktails of GFs enhanced expression of cardiac transcription factors and survival. Induction of cardiac specific markers by coculture with CMCs and gap junctional communication with CMCs was more active in GF-treated MSCs than untreated MSCs. The GF-treated MSCs reduced apoptosis of neighboring CMCs in a hypoxic condition and enhanced the phosphorylated Akt and phosphorylated c-AMP response element binding protein expression of CMCs, which was markedly reduced by gap junction blockade. In a rat myocardial infarction model, transplantation of GF-treated MSCs resulted in smaller infarct size and better cardiac function than transplantation of untreated MSCs. Additionally, GF treatment enhanced gap junction formation of transplanted MSCs, which did not aggravate arrhythmia. CONCLUSIONS: Pre-treatment of MSCs with GFs enhanced cytoprotective effects on neighboring CMCs through gap junction and improved the therapeutic efficacy of MSC transplantation for myocardial repair. "Priming of MSCs with GFs" before transplantation might improve the therapeutic efficacy of cell therapy.
机译:目的:本研究的目的是研究用生长因子(GFs)预处理间充质干细胞(MSCs)对心肌分化,对心肌细胞(CMCs)的细胞保护作用及其在心肌梗塞中的治疗效果。背景:MSC移植修复心肌的机制尚未完全阐明,需要提高治疗效果。方法:将Fisher344大鼠骨髓中的MSCs分别用成纤维细胞生长因子2,胰岛素样生长因子-1和骨形态发生蛋白2处理。评价了心脏特异性标志物的表达和MSCs的保护作用及其机制。在大鼠心肌梗死模型中研究了MSCs移植的功效。结果:GFs鸡尾酒治疗MSCs增强心脏转录因子的表达和生存。与未处理的MSC相比,在GF处理的MSC中通过与CMC共培养和与CMC的间隙连接通讯诱导心脏特异性标志物更为活跃。在缺氧条件下,经GF处理的MSC减少了邻近CMC的凋亡,并增强了CMC的磷酸化Akt和磷酸化c-AMP反应元件结合蛋白的表达,这被间隙连接阻断显着降低。在大鼠心肌梗死模型中,与未治疗的MSC相比,GF治疗的MSC的移植导致更小的梗塞面积和更好的心脏功能。此外,GF治疗增强了移植的MSC的间隙连接形成,但并未加剧心律不齐。结论GFs预处理MSCs通过间隙连接增强了对邻近CMCs的细胞保护作用,提高了MSCs移植修复心肌的疗效。移植前“用GF灌注MSC”可能会提高细胞治疗的疗效。

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