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首页> 外文期刊>Aging and Disease >Hydrogen Peroxide-Induced Senescence Reduces the Wound Healing-Promoting Effects of Mesenchymal Stem Cell-Derived Exosomes Partially via miR-146a
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Hydrogen Peroxide-Induced Senescence Reduces the Wound Healing-Promoting Effects of Mesenchymal Stem Cell-Derived Exosomes Partially via miR-146a

机译:过氧化氢诱导的衰老降低了通过MIR-146A部分地通过MIR-146a部分地通过MIR-146a降低了间充质干细胞衍生的外泌体的伤口愈合促进作用

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摘要

Mesenchymal stem cells (MSCs) have beneficial effects on wound healing. MSCs function through direct cell-cell communication or indirectly through paracrine secretion of exosomes. Here, we found that MSC-derived exosomes had pro-wound healing effects via promotion of angiogenesis; however, this promoting effect was significantly reduced when senescence was induced in parental MSCs by hydrogen peroxide (H 2 O 2 ). Further experiments showed that decreased miR-146a expression in exosomes derived from senescent MSCs (s-exo) contributed to these findings. In vitro, the pro-angiogenic effect of s-exo on tube formation in human umbilical vein endothelial cells was significantly reduced compared with that of exosomes derived from control MSCs (c-exo). In vivo, higher tube numbers and longer tube lengths were observed in the c-exo group compared with the s-exo group. Using microarray analysis, we found that miR-146a level in s-exo was lower than that in c-exo. Knockdown of miR-146a in c-exo decreased its capacity to promote angiogenesis, and overexpression of miR-146a in s-exo partially rescued its impaired pro-angiogenic capacity, thereby confirming that downregulation of miR-146a contributed to the reduced pro-wound healing capacity of s-exo. Our study is the first to demonstrate that cell senescence induced by H 2 O 2 alters the pro-angiogenic ability of exosomes by modulating the expression of exosomal miRNAs, especially miR-146a, thus providing new insights into the correlation between parental cell state and exosome content and function.copyright: ? 2021 Xu et al.
机译:间充质干细胞(MSCs)对伤口愈合具有有益作用。 MSCS通过直接细胞 - 细胞通信或间接通过外甲烷的分泌物间接函数。在这里,我们发现MSC衍生的外泌体通过促进血管生成具有促伤愈合效应;然而,当通过过氧化氢(H 2 O 2)在亲本MSC中诱导衰老时,这种促进效果显着降低。进一步的实验表明,衍生自衰老MSCs(S-EXO)的外泌体中的miR-146a表达减少有助于这些发现。体外,与来自对照MSCs(C-EXO)的外来体相比,S-EXO对人脐静脉内皮细胞管形成的促血管生成效果显着降低(C-EXO)。与S-EXO组相比,在C-EXO组中观察到较高管数和较长的管长度。使用微阵列分析,我们发现S-EXO中的MIR-146A水平低于C-EXO。 C-EXO中MiR-146a的敲低降低了其促进血管生成的能力,并且S-EXO中miR-146a的过表达部分地拯救了其受损的促血管生成能力,从而证实miR-146a的下调导致减少的培训减少S-EXO的愈合能力。我们的研究是首先证明由H 2 O 2诱导的细胞衰老通过调节外泌体miRNA,尤其是miR-146a的表达而改变外来体的促血管生成能力,从而为亲本细胞状态和外出组之间的相关性提供了新的洞察力内容和函数。柔小妙语:? 2021 Xu等人。

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