微泡
干细胞
血管生成
外体
伤口愈合
Wnt信号通路
间充质干细胞
医学
脂肪组织
癌症研究
干细胞疗法
细胞疗法
小RNA
化学
细胞生物学
药理学
免疫学
病理
信号转导
生物
内科学
基因
生物化学
作者
Qijun Lv,Junfeng Deng,You Chen,Yizhen Wang,Бо Лю,Jie Liu
标识
DOI:10.1021/acs.molpharmaceut.0c00177
摘要
Diabetic wounds are a worldwide health problem causing extremely heavy public health burden and require effective treatment. Optimal strategies for treating nonhealing diabetic wounds include stem-cell-based therapy and delivery of novel drug substances, such as functional microRNAs (miRNAs); however, miRNA easily degrades in the wound microenvironment. Herein, we developed a human adipose stem-cell-derived exosome (hASC-exos)-based miRNA delivery strategy to enhance its therapeutic efficacy. The miR-21-5p mimics, as novel therapeutic candidates for diabetic wounds, were loaded into hASC-exos by electroporation, taking advantage of natural availability and biocompatibility of exosomes as extracellular miRNA transporting particles. The engineered exosomes (E-exos) exhibited excellent effects on promoting proliferation and migration of keratinocytes via Wnt/β-catenin signaling in vitro and accelerating diabetic wound healing by increasing re-epithelialization, collagen remodeling, angiogenesis, and vessel maturation in vivo. Results from this study would set the fundamentals of applying hASC-exos to deliver future drug substances and to develop cell-free therapy for wound-healing treatments.
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