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 alpha 7/beta 1 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.
Millozzi, F., Milán-Rois, P., Sett, A., Delli Carpini, G., De Bardi, M., Gisbert-Garzarán, M., Sandona', M., Rodríguez-Díaz, C., Martínez-Mingo, M., Pardo, I., Esposito, F., Viscomi, M. T., Bouché, M., Parolini, O., Saccone, V., Toulmé, J. J., Somoza, Á., Palacios, D., Aptamer-conjugated gold nanoparticles enable oligonucleotide delivery into muscle stem cells to promote regeneration of dystrophic muscles, <<NATURE COMMUNICATIONS>>, 2025; 16 (1): N/A-N/A. [doi:10.1038/s41467-024-55223-9] [https://hdl.handle.net/10807/312042]
Aptamer-conjugated gold nanoparticles enable oligonucleotide delivery into muscle stem cells to promote regeneration of dystrophic muscles
Millozzi, Francesco;Delli Carpini, Giovanni;Sandona', Martina;Viscomi, Maria Teresa;Parolini, Ornella;Saccone, Valentina;
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 alpha 7/beta 1 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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