| Literature DB >> 32233440 |
Qijun Lv1, Junfeng Deng1, You Chen2, Yizhen Wang1, Bo Liu1, Jie Liu2.
Abstract
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.Entities:
Keywords: adipose stem cells; diabetic wound healing; engineered exosomes; miR-21; re-epithelialization
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Year: 2020 PMID: 32233440 DOI: 10.1021/acs.molpharmaceut.0c00177
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939