Aptamer-conjugated gold nanoparticles enable oligonucleotide delivery into muscle stem cells to promote regeneration of dystrophic muscles

Nat Commun. 2025 Jan 10;16(1):577. doi: 10.1038/s41467-024-55223-9.

Abstract

Inefficient targeting of muscle stem cells (MuSCs), also called satellite cells, represents a major bottleneck of current therapeutic strategies for muscular dystrophies, as it precludes the possibility of promoting compensatory regeneration. Here we describe a muscle-targeting delivery platform, based on gold nanoparticles, that enables the release of therapeutic oligonucleotides into MuSCs. We demonstrate that AuNPs conjugation to an aptamer against α7/β1 integrin dimers directs either local or systemic delivery of microRNA-206 to MuSCs, thereby promoting muscle regeneration and improving muscle functionality, in a mouse model of Duchenne Muscular Dystrophy. We show here that this platform is biocompatible, non-toxic, and non-immunogenic, and it can be easily adapted for the release of a wide range of therapeutic oligonucleotides into diseased muscles.

MeSH terms

  • Animals
  • Aptamers, Nucleotide* / administration & dosage
  • Aptamers, Nucleotide* / chemistry
  • Disease Models, Animal
  • Gold* / chemistry
  • Humans
  • Male
  • Metal Nanoparticles* / chemistry
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred mdx
  • MicroRNAs* / administration & dosage
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Muscle, Skeletal* / metabolism
  • Muscular Dystrophy, Duchenne* / metabolism
  • Muscular Dystrophy, Duchenne* / therapy
  • Oligonucleotides / administration & dosage
  • Regeneration*
  • Satellite Cells, Skeletal Muscle / metabolism
  • Stem Cells / cytology
  • Stem Cells / metabolism

Substances

  • Gold
  • Aptamers, Nucleotide
  • MicroRNAs
  • Oligonucleotides