哈卡特
伤口愈合
间充质干细胞
细胞周期蛋白依赖激酶6
小RNA
细胞生物学
细胞生长
人体皮肤
脂肪组织
细胞凋亡
皮肤修复
微泡
外体
癌症研究
免疫学
化学
医学
生物
体外
细胞周期
生物化学
细胞周期蛋白依赖激酶
基因
遗传学
作者
Xin Liao,Fei Yan,Sean Hu,Jian Mu,Siqiaozhi Li,Yijie He,Manshu Tang,Junhui Chen,Lian Yu,Jia Sun
出处
期刊:Biomaterials advances
日期:2022-05-01
卷期号:136: 212781-212781
被引量:3
标识
DOI:10.1016/j.bioadv.2022.212781
摘要
Application of adipose-derived mesenchymal stromal cells (AMSCs)-derived extracellular vesicles (EVs) in skin wound healing has been documented. In this study, we investigated the therapeutic potential of AMSCs-derived EVs in skin wound healing through delivery of microRNA-10b (miR-10b). HaCaT cells were treated with H2O2 to establish the skin wound cell models. Next, the binding affinity between miR-194, PEA15, and CDK6 was identified. Additionally, EVs were isolated from the culture medium of AMSC sheets, followed by incubation with H2O2-treated HaCaT cells to detect cell proliferation, migration, and apoptosis using gain- or loss-of-function experiments. Lastly, the mice skin wound models were also established to assess skin wound healing ability. miR-10b was down-regulated in the skin trauma models and enriched in the EVs of AMSC sheets. Moreover, miR-10b derived from EVs targeted PEA15 to promote CDK6 expression, thereby stimulating the proliferation and migration of H2O2-damaged HaCaT cells but inhibiting apoptosis. In vivo experiments further ascertained the therapeutic functionality of AMSC sheets-derived EVs-miR-10b. In summary, AMSC sheets-derived EVs carrying miR-10b promoted CDK6 expression to intensify skin wound healing by regulating PEA15.
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