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Exosomes from adipose-derived mesenchymal stem cells prevent cardiomyocyte apoptosis induced by oxidative stress

机译:脂肪间充质干细胞的外来体可防止氧化应激诱导的心肌细胞凋亡

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Exosomes from bone marrow stem cells or cardiac progenitor cells can reduce apoptosis in myocardial cells after ischemia and reperfusion injury. However, there is little known about the effects of exosomes from adipose-derived stem cells (ADSCs), which are more abundant and have a lower risk of side effects. The aim of this study was to characterize exosomes from ADSCs and evaluate their cardioprotective actions against ischemia reperfusion injury. The exosomes were isolated from ADSCs and analyzed by protein marker expression, transmission electron microscopy, and nanoparticle tracking analysis. The ADSC-exosomes were then used for ex vivo investigation of the cardioprotective effects on cardiomyocytes after exposure to oxidative stress. Exosomes from ADSCs exhibited a diameter of 150?nm and expressed the marker proteins, CD9 and CD29. ADSC-exosomes had no effect on proliferation of untreated cardiomyocytes. In contrast, ADSC-derived exosomes reduced apoptosis in myocardial cells subjected to oxidative stress. This study confirms that exosomes originating from ADSCs can protect cardiomyocytes from oxidative stress.
机译:骨髓干细胞或心脏祖细胞的外来体可以减少缺血和再灌注损伤后心肌细胞的凋亡。但是,关于来自脂肪干细胞(ADSC)的外泌体的作用鲜为人知,这种外泌体更为丰富且具有较低的副作用风险。这项研究的目的是表征ADSC的外泌体并评估其对缺血再灌注损伤的心脏保护作用。从ADSCs中分离出外泌体,并通过蛋白质标志物表达,透射电子显微镜和纳米颗粒跟踪分析进行分析。然后将ADSC-外泌体用于体外研究暴露于氧化应激后对心肌细胞的心脏保护作用。来自ADSC的外泌体显示出直径为150μm,并表达标记蛋白CD9和CD29。 ADSC外泌体对未经处理的心肌细胞的增殖没有影响。相反,ADSC衍生的外来体减少了遭受氧化应激的心肌细胞的凋亡。这项研究证实,源自ADSC的外泌体可以保护心肌细胞免受氧化应激。

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