Department of General Surgery, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510120, China.
School of Biomedical Engineering, Sun Yat-sen University, Guangzhou, Guangdong 510006, China.
Mol Pharm. 2020 May 4;17(5):1723-1733. doi: 10.1021/acs.molpharmaceut.0c00177. Epub 2020 Apr 13.
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.
糖尿病伤口是一个全球性的健康问题,给公共卫生带来了极其沉重的负担,需要有效的治疗。治疗非愈合性糖尿病伤口的最佳策略包括基于干细胞的治疗和新型药物物质的递送,如功能性 microRNAs(miRNAs);然而,miRNA 在伤口微环境中容易降解。在此,我们开发了一种基于人脂肪干细胞衍生的外泌体(hASC-exos)的 miRNA 递送策略,以增强其治疗效果。miR-21-5p 模拟物作为糖尿病伤口的新型治疗候选物,通过电穿孔被加载到 hASC-exos 中,利用外泌体作为细胞外 miRNA 转运颗粒的天然可用性和生物相容性。工程化的外泌体(E-exos)在体外通过 Wnt/β-catenin 信号通路显著促进角质形成细胞的增殖和迁移,并通过增加再上皮化、胶原重塑、血管生成和血管成熟来加速糖尿病伤口愈合。本研究的结果将为应用 hASC-exos 递送未来药物物质和开发无细胞治疗伤口愈合奠定基础。