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过氧化氢诱导的衰老通过miR-146a部分降低间充质干细胞衍生外泌体促进伤口愈合的作用。

Hydrogen Peroxide-Induced Senescence Reduces the Wound Healing-Promoting Effects of Mesenchymal Stem Cell-Derived Exosomes Partially via miR-146a.

作者信息

Xu Meiqian, Su Xiaodong, Xiao Xian, Yu Hongliang, Li Xiaoxia, Keating Armand, Wang Shihua, Zhao Robert Chunhua

机构信息

1Institute of Basic Medical Sciences Chinese Academy of Medical Sciences,School of Basic Medicine Peking Union Medical College, Center of Excellence in Tissue Engineering Chinese Academy of Medical Sciences, Beijing 100005, China.

2Brain Tumor Research Center, Beijing Neurosurgical Institute, Beijing Tiantan Hospital Affiliated to Capital Medical University, Beijing Laboratory of Biomedical Materials, Beijing 100070, China.

出版信息

Aging Dis. 2021 Feb 1;12(1):102-115. doi: 10.14336/AD.2020.0624. eCollection 2021 Feb.

Abstract

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 (HO). Further experiments showed that decreased miR-146a expression in exosomes derived from senescent MSCs (s-exo) contributed to these findings. , 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). , 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 HO 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.

摘要

间充质干细胞(MSCs)对伤口愈合具有有益作用。MSCs通过直接的细胞间通讯或通过外泌体的旁分泌间接发挥作用。在此,我们发现MSCs来源的外泌体通过促进血管生成具有促进伤口愈合的作用;然而,当用过氧化氢(HO)诱导亲代MSCs衰老时,这种促进作用显著降低。进一步的实验表明,衰老MSCs(s-exo)来源的外泌体中miR-146a表达降低导致了这些结果。与对照MSCs(c-exo)来源的外泌体相比,s-exo对人脐静脉内皮细胞管形成的促血管生成作用显著降低。与s-exo组相比,c-exo组观察到更高的管数量和更长的管长度。通过微阵列分析,我们发现s-exo中的miR-146a水平低于c-exo。敲低c-exo中的miR-146a降低了其促进血管生成的能力,而在s-exo中过表达miR-146a部分挽救了其受损的促血管生成能力,从而证实miR-146a的下调导致了s-exo促伤口愈合能力的降低。我们的研究首次证明,HO诱导的细胞衰老通过调节外泌体miRNA的表达,特别是miR-146a,改变了外泌体的促血管生成能力,从而为亲代细胞状态与外泌体含量和功能之间的相关性提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd15/7801275/1f93ac0bee40/ad-12-1-102-g1.jpg

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