TY - JOUR
T1 - Localization of magic-F1 transgene, involved in muscular hypertrophy, during early myogenesis
AU - Ronzoni, Flavio
AU - Bongio, Matilde
AU - Conte, Silvio
AU - Vercesi, Luigi
AU - Cassano, Marco
AU - Tribioli, Carla
AU - Galli, Daniela
AU - Bellazzi, Riccardo
AU - Magenes, Giovanni
AU - Cusella De Angelis, Maria Gabriella
AU - Sampaolesi, Maurilio
PY - 2011
Y1 - 2011
N2 - We recently showed that Magic-F1 (Met-activating genetically improved chimeric factor 1), a human recombinant protein derived from hepatocyte growth factor/scatter factor (HGF/SF) induces muscle cell hypertrophy but not progenitor cell proliferation, both in vitro and in vivo. Here, we examined the temporal and spatial expression pattern of Magic-F1 in comparison with Pax3 (paired box gene 3) transcription factor during embryogenesis. Ranging from 9.5 to 17.5dpc (days post coitum) mouse embryos were analyzed by in situ hybridization using whole mounts during early stages of development (9.5-10.5-11.5dpc) and cryostat sections for later stages (11.5-13.5-15.5-17. 5dpc). We found that Magic-F1 is expressed in developing organs and tissues of mesenchymal origin, where Pax3 signal appears to be downregulated respect to the wt embryos. These data suggest that Magic-F1 could be responsible of muscular hypertrophy, cooperating with Pax3 signal pathway in skeletal muscle precursor cells.
AB - We recently showed that Magic-F1 (Met-activating genetically improved chimeric factor 1), a human recombinant protein derived from hepatocyte growth factor/scatter factor (HGF/SF) induces muscle cell hypertrophy but not progenitor cell proliferation, both in vitro and in vivo. Here, we examined the temporal and spatial expression pattern of Magic-F1 in comparison with Pax3 (paired box gene 3) transcription factor during embryogenesis. Ranging from 9.5 to 17.5dpc (days post coitum) mouse embryos were analyzed by in situ hybridization using whole mounts during early stages of development (9.5-10.5-11.5dpc) and cryostat sections for later stages (11.5-13.5-15.5-17. 5dpc). We found that Magic-F1 is expressed in developing organs and tissues of mesenchymal origin, where Pax3 signal appears to be downregulated respect to the wt embryos. These data suggest that Magic-F1 could be responsible of muscular hypertrophy, cooperating with Pax3 signal pathway in skeletal muscle precursor cells.
UR - http://www.scopus.com/inward/record.url?scp=84855535726&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84855535726&partnerID=8YFLogxK
U2 - 10.1155/2011/492075
DO - 10.1155/2011/492075
M3 - Article
C2 - 22187527
AN - SCOPUS:84855535726
SN - 1110-7243
VL - 2011
JO - Journal of Biomedicine and Biotechnology
JF - Journal of Biomedicine and Biotechnology
M1 - 492075
ER -