: 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.
Aptamer-conjugated gold nanoparticles enable oligonucleotide delivery into muscle stem cells to promote regeneration of dystrophic muscles / Millozzi, Francesco; Milán-Rois, Paula; Sett, Arghya; Delli Carpini, Giovanni; De Bardi, Marco; Gisbert-Garzarán, Miguel; Sandonà, Martina; Rodríguez-Díaz, Ciro; Martínez-Mingo, Mario; Pardo, Irene; Esposito, Federica; Viscomi, Maria Teresa; Bouche, Marina; Parolini, Ornella; Saccone, Valentina; Toulmé, Jean-Jacques; Somoza, Álvaro; Palacios, Daniela. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - 16:1(2025), pp. 1-19. [10.1038/s41467-024-55223-9]
Aptamer-conjugated gold nanoparticles enable oligonucleotide delivery into muscle stem cells to promote regeneration of dystrophic muscles
Millozzi, Francesco;Bouche, Marina;
2025
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.File | Dimensione | Formato | |
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