间充质干细胞
微泡
基因敲除
外体
血管生成
癌症研究
伤口愈合
小RNA
体内
PI3K/AKT/mTOR通路
细胞生物学
蛋白激酶B
化学
信号转导
医学
生物
免疫学
细胞凋亡
生物化学
生物技术
基因
作者
Qiqi Zhang,Peng Su,Feng Zhao,Haiyue Ren,Cai He,Wu Quan,Zitong Wang,Jiajie Ma,Xing Huang,Zhe Wang
标识
DOI:10.1021/acsbiomaterials.3c01567
摘要
The use of exosomes to relieve skin injuries has received considerable attention. The PluronicF-127 hydrogel (PF-127 hydrogel) is a novel biomaterial that can be used to carry biomolecules. This study sought to investigate the impact of exosomes originating from human mesenchymal stem cells (MSCs) developed from adipose tissue (hADSC-Exos) combined with a PF-127 hydrogel on tissue repair and explore the underlying mechanism using in vitro and in vivo experiments. miR-148a-3p is the most expressed microRNA (miRNA) in hADSC-Exos. We found that exosomes combined with the PF-127 hydrogel had a better efficacy than exosomes alone; moreover, miR-148a-3p knockdown lowered its efficacy. In vitro, we observed a significant increase in the tumor-like ability of HUVECs after exosome treatment, which was attenuated after miR-148a-3p knockdown. Furthermore, the effects of miR-148a-3p on hADSC-Exos were achieved through the prevention of PTEN and the triggering of phosphatidylinositol 3-kinase (PI3K)/Akt signaling. In conclusion, our results demonstrated that hADSC-Exos can promote angiogenesis and skin wound healing by delivering miR-148a-3p and have a better effect when combined with the PF-127 hydrogel, which may be an alternative strategy to promote wound healing.
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