首页> 美国卫生研究院文献>International Journal of Molecular Sciences >MicroRNA-Mediated Down-Regulation of Apoptosis Signal-Regulating Kinase 1 (ASK1) Attenuates the Apoptosis of Human Mesenchymal Stem Cells (MSCs) Transplanted into Infarcted Heart
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MicroRNA-Mediated Down-Regulation of Apoptosis Signal-Regulating Kinase 1 (ASK1) Attenuates the Apoptosis of Human Mesenchymal Stem Cells (MSCs) Transplanted into Infarcted Heart

机译:MicroRNA介导的凋亡信号调节激酶1(ASK1)的下调减弱了移植到梗塞心脏的人间充质干细胞(MSC)的凋亡。

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摘要

Stem cell therapy using adult stem cells, such as mesenchymal stem cells (MSCs) has produced some promising results in treating the damaged heart. However, the low survival rate of MSCs after transplantation is still one of the crucial factors that limit the therapeutic effect of stem cells. In the damaged heart, oxidative stress due to reactive oxygen species (ROS) production can cause the death of transplanted MSCs. Apoptosis signal-regulating kinase 1 (ASK1) has been implicated in the development of oxidative stress-related pathologic conditions. Thus, we hypothesized that down-regulation of ASK1 in human MSCs (hMSCs) might attenuate the post-transplantation death of MSCs. To test this hypothesis, we screened microRNAs (miRNAs) based on a miRNA-target prediction database and empirical data and investigated the anti-apoptotic effect of selected miRNAs on human adipose-derived stem cells (hASCs) and on rat myocardial infarction (MI) models. Our data indicated that miRNA-301a most significantly suppressed ASK1 expression in hASCs. Apoptosis-related genes were significantly down-regulated in miRNA-301a-enriched hASCs exposed to hypoxic conditions. Taken together, these data show that miRNA-mediated down-regulation of ASK1 protects MSCs during post-transplantation, leading to an increase in the efficacy of MSC-based cell therapy.
机译:使用成体干细胞(例如间充质干细胞(MSCs))进行干细胞治疗已在治疗受损心脏方面产生了一些有希望的结果。然而,MSCs移植后的低存活率仍然是限制干细胞治疗效果的关键因素之一。在受损的心脏中,由于活性氧(ROS)产生而产生的氧化应激会导致移植的MSC死亡。凋亡信号调节激酶1(ASK1)已被证明与氧化应激相关的病理状况的发展。因此,我们假设人类MSC(hMSCs)中ASK1的下调可能会减轻MSCs的移植后死亡。为了验证这一假设,我们基于miRNA靶预测数据库和经验数据筛选了microRNA(miRNA),并研究了选定的miRNA对人脂肪干细胞(hASCs)和大鼠心肌梗死(MI)的抗凋亡作用。楷模。我们的数据表明,miRNA-301a最能抑制hASC中的ASK1表达。在暴露于低氧条件下富含miRNA-301a的hASC中,与凋亡相关的基因显着下调。综上所述,这些数据表明,miRNA介导的ASK1的下调在移植后可保护MSC,从而导致基于MSC的细胞治疗功效提高。

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