Exosome-like vesicles encapsulated with specific microRNAs accelerate burn wound healing and ameliorate scarring

J Nanobiotechnology. 2025 Apr 2;23(1):264. doi: 10.1186/s12951-025-03337-7.

Abstract

Burn injuries are prevalent, yet effective treatments remain elusive. Exosomes derived from mesenchymal stem cells (MSC-Ex) possess remarkable pro-regenerative properties for wound healing. Despite their potential, the challenge of mass production limits their clinical application. To address this, preparing exosome-like vesicles has become an international trend. In this study, 28 key microRNAs (miRNAs) with significant pro-proliferation, anti-inflammation, and anti-fibrosis functions were screened from MSC-Ex. These miRNAs were encapsulated into liposomes and then hybridized with extracellular vesicles derived from watermelon to create synthetic exosome-like vesicles. The fabricated vesicles exhibited similar particle size and zeta potential to MSC-Ex, demonstrating high serum stability and effectively resisting the degradation of miRNA by RNase. They were efficiently internalized by cells and enabled a high rate of lysosomal escape for miRNAs post cellular uptake, thereby effectively exerting their pro-proliferative, anti-inflammatory, and anti-fibrotic functions. Further experiments demonstrated that these vesicles efficiently accelerated burn wound healing and reduced scarring, with effects comparable to those of natural MSC-Ex. Based on these findings, the exosome-like vesicles fabricated in this study present a promising alternative to MSC-Ex in burn wound treatment.

Keywords: Exosome-like vesicles; Exosomes; Mesenchymal stem cells; Scar; Wound; microRNA.

MeSH terms

  • Animals
  • Burns* / pathology
  • Burns* / therapy
  • Cell Proliferation / drug effects
  • Cicatrix*
  • Exosomes* / chemistry
  • Exosomes* / metabolism
  • Humans
  • Liposomes / chemistry
  • Male
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • MicroRNAs* / chemistry
  • MicroRNAs* / metabolism
  • MicroRNAs* / pharmacology
  • Wound Healing* / drug effects

Substances

  • MicroRNAs
  • Liposomes