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微小RNA介导的凋亡信号调节激酶1(ASK1)下调减轻移植到梗死心脏中的人间充质干细胞(MSC)凋亡。

MicroRNA-Mediated Down-Regulation of Apoptosis Signal-Regulating Kinase 1 (ASK1) Attenuates the Apoptosis of Human Mesenchymal Stem Cells (MSCs) Transplanted into Infarcted Heart.

作者信息

Lee Chang Youn, Shin Sunhye, Lee Jiyun, Seo Hyang-Hee, Lim Kyu Hee, Kim Hyemin, Choi Jung-Won, Kim Sang Woo, Lee Seahyung, Lim Soyeon, Hwang Ki-Chul

机构信息

Department of Integrated Omics for Biomedical Sciences, Yonsei University, 03722 Seoul, Korea.

Brain Korea 21 PLUS Project for Medical Science, Yonsei University, 03722 Seoul, Korea.

出版信息

Int J Mol Sci. 2016 Oct 20;17(10):1752. doi: 10.3390/ijms17101752.

Abstract

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.

摘要

使用成体干细胞(如间充质干细胞(MSC))进行干细胞治疗在治疗受损心脏方面已取得了一些有前景的成果。然而,移植后MSC的低存活率仍然是限制干细胞治疗效果的关键因素之一。在受损心脏中,活性氧(ROS)产生导致的氧化应激可引起移植的MSC死亡。凋亡信号调节激酶1(ASK1)与氧化应激相关病理状况的发展有关。因此,我们假设在人MSC(hMSC)中下调ASK1可能会减轻移植后MSC的死亡。为了验证这一假设,我们基于miRNA靶点预测数据库和实验数据筛选了微小RNA(miRNA),并研究了所选miRNA对人脂肪来源干细胞(hASC)和大鼠心肌梗死(MI)模型的抗凋亡作用。我们的数据表明,miRNA-301a在hASC中最显著地抑制ASK1表达。在暴露于缺氧条件的富含miRNA-301a的hASC中,凋亡相关基因显著下调。综上所述,这些数据表明,miRNA介导的ASK1下调在移植后保护MSC,从而提高基于MSC的细胞治疗的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7014/5085777/cdbe7eb6c97e/ijms-17-01752-g001.jpg

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