The recent advances, offered by cell therapy in the regenerative medicine field, offer a revolutionary potential for the development of innovative cures to restore compromised physiological functions or organs. Adult myogenic precursors, such as myoblasts or satellite cells, possess a marked regenerative capacity, but the exploitation of this potential still encounters significant challenges in clinical application, due to low rate of proliferation in vitro, as well as a reduced self-renewal capacity. In this scenario, induced pluripotent stem cells (iPSCs) can offer not only an inexhaustible source of cells for regenerative therapeutic approaches, but also a valuable alternative for in vitro modeling of patient-specific diseases. In this study we established a reliable protocol to induce the myogenic differentiation of iPSCs, generated from pericytes and fibroblasts, exploiting skeletal muscle-derived extracellular vesicles (EVs), in combination with chemically defined factors. This genetic integration-free approach generates functional skeletal myotubes maintaining the engraftment ability in vivo. Our results demonstrate evidence that EVs can act as biological “shuttles” to deliver specific bioactive molecules for a successful transgene-free differentiation offering new opportunities for disease modeling and regenerative approaches.

Baci, D., Chirivì, M., Pace, V., Maiullari, F., Milan, M., Rampin, A., et al. (2020). Extracellular vesicles from skeletal muscle cells efficiently promote myogenesis in induced pluripotent stem cells. CELLS, 9(6) [10.3390/cells9061527].

Extracellular vesicles from skeletal muscle cells efficiently promote myogenesis in induced pluripotent stem cells

Baci, Denisa;Cannata, Stefano;Gargioli, Cesare;
2020-01-01

Abstract

The recent advances, offered by cell therapy in the regenerative medicine field, offer a revolutionary potential for the development of innovative cures to restore compromised physiological functions or organs. Adult myogenic precursors, such as myoblasts or satellite cells, possess a marked regenerative capacity, but the exploitation of this potential still encounters significant challenges in clinical application, due to low rate of proliferation in vitro, as well as a reduced self-renewal capacity. In this scenario, induced pluripotent stem cells (iPSCs) can offer not only an inexhaustible source of cells for regenerative therapeutic approaches, but also a valuable alternative for in vitro modeling of patient-specific diseases. In this study we established a reliable protocol to induce the myogenic differentiation of iPSCs, generated from pericytes and fibroblasts, exploiting skeletal muscle-derived extracellular vesicles (EVs), in combination with chemically defined factors. This genetic integration-free approach generates functional skeletal myotubes maintaining the engraftment ability in vivo. Our results demonstrate evidence that EVs can act as biological “shuttles” to deliver specific bioactive molecules for a successful transgene-free differentiation offering new opportunities for disease modeling and regenerative approaches.
2020
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/05 - ZOOLOGIA
English
Con Impact Factor ISI
iPSC; extracellular vesicles; pericytes; skeletal muscle
Baci, D., Chirivì, M., Pace, V., Maiullari, F., Milan, M., Rampin, A., et al. (2020). Extracellular vesicles from skeletal muscle cells efficiently promote myogenesis in induced pluripotent stem cells. CELLS, 9(6) [10.3390/cells9061527].
Baci, D; Chirivì, M; Pace, V; Maiullari, F; Milan, M; Rampin, A; Somma, P; Presutti, D; Garavelli, S; Bruno, A; Cannata, S; Lanzuolo, C; Gargioli, C; Rizzi, R; Bearzi, C
Articolo su rivista
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/251137
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 15
  • ???jsp.display-item.citation.isi??? 12
social impact