Met Activating Genetically Improved Chimeric Factor 1 (Magic-F1) is a human recombinant protein, derived from dimerization of the receptor-binding domain of hepatocyte growth factor. Previous experiments demonstrate that in transgenic mice, the skeletal muscle specific expression of Magic-F1 can induce a constitutive muscular hypertrophy, improving running performance and accelerating muscle regeneration after injury. In order to evaluate the therapeutic potential of Magic-F1, we tested its effect on multipotent and pluripotent stem cells. In murine mesoangioblasts (adult vessel-associated stem cells), the presence of Magic-F1 did not alter their osteogenic, adipogenic or smooth muscle differentiation ability. However, when analyzing their myogenic potential, mesoangioblasts expressing Magic-F1 differentiated spontaneously into myotubes. Finally, Magic-F1 inducible cassette was inserted into a murine embryonic stem cell line by homologous recombination. When embryonic stem cells were subjected to myogenic differentiation, the presence of Magic-F1 resulted in the upregulation of Pax3 and Pax7 that enhanced the myogenic commitment of transgenic pluripotent stem cells. Taken together our results candidate Magic-F1 as a potent myogenic stimulator, able to enhance muscular differentiation from both adult and pluripotent stem cells.

Myogenic induction of adult and pluripotent stem cells using recombinant proteins / Perini, Ilaria; Elia, Ilaria; Lo Nigro, Antonio; Ronzoni, FLAVIO LORENZO; Berardi, Emanuele; Grosemans, Hanne; Fukada, So Ichiro; Sampaolesi, Maurilio. - In: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. - ISSN 0006-291X. - 464:3(2015), pp. 755-761. [10.1016/j.bbrc.2015.07.022]

Myogenic induction of adult and pluripotent stem cells using recombinant proteins

SAMPAOLESI, MAURILIO
2015

Abstract

Met Activating Genetically Improved Chimeric Factor 1 (Magic-F1) is a human recombinant protein, derived from dimerization of the receptor-binding domain of hepatocyte growth factor. Previous experiments demonstrate that in transgenic mice, the skeletal muscle specific expression of Magic-F1 can induce a constitutive muscular hypertrophy, improving running performance and accelerating muscle regeneration after injury. In order to evaluate the therapeutic potential of Magic-F1, we tested its effect on multipotent and pluripotent stem cells. In murine mesoangioblasts (adult vessel-associated stem cells), the presence of Magic-F1 did not alter their osteogenic, adipogenic or smooth muscle differentiation ability. However, when analyzing their myogenic potential, mesoangioblasts expressing Magic-F1 differentiated spontaneously into myotubes. Finally, Magic-F1 inducible cassette was inserted into a murine embryonic stem cell line by homologous recombination. When embryonic stem cells were subjected to myogenic differentiation, the presence of Magic-F1 resulted in the upregulation of Pax3 and Pax7 that enhanced the myogenic commitment of transgenic pluripotent stem cells. Taken together our results candidate Magic-F1 as a potent myogenic stimulator, able to enhance muscular differentiation from both adult and pluripotent stem cells.
2015
embryonic stem cells; magic-F1; mesoangioblast; myogenic differentiation; recombinant protein; adult stem cells; animals; cell differentiation; cell line; green fluorescent proteins; HEK293 cells; hepatocyte growth factor; humans; mice; transgenic; muscle development; PAX7 transcription factor; paired box transcription factors; pluripotent stem cells; recombinant proteins; up-regulation; biochemistry; biophysics; cell biology; molecular biology; medicine (all)
01 Pubblicazione su rivista::01a Articolo in rivista
Myogenic induction of adult and pluripotent stem cells using recombinant proteins / Perini, Ilaria; Elia, Ilaria; Lo Nigro, Antonio; Ronzoni, FLAVIO LORENZO; Berardi, Emanuele; Grosemans, Hanne; Fukada, So Ichiro; Sampaolesi, Maurilio. - In: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. - ISSN 0006-291X. - 464:3(2015), pp. 755-761. [10.1016/j.bbrc.2015.07.022]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1582069
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