TY - JOUR
T1 - Monitor of the myostatin autocrine action during differentiation of embryonic chicken myoblasts into myotubes
T2 - Effect of IGF-I
AU - Kurokawa, Masatoshi
AU - Sato, Fuminori
AU - Aramaki, Shinya
AU - Soh, Tomoki
AU - Yamauchi, Nobuhiko
AU - Hattori, Masa Aki
N1 - Funding Information:
Acknowledgments This research was supported in part by a Grant-in-Aid for Scientific Research (B) from the Japan Society for the Promotion of Sciences (JSPS; 16380200) (to M.-A. Hattori). F. Sato and S. Aramaki were, respectively, supported by Research Fellowships of the Japan Society for the Promotion of Science for Young Scientists (No. 166796 and No. 09744).
PY - 2009
Y1 - 2009
N2 - Myogenesis is regulated through the proliferation and differentiation of myoblasts expressing myostatin which functions as a negative regulator by generating Smad signals. Here, we monitored the autocrine action of myostatin in quiescent chicken myoblasts transfected with the Smad-mediated promoter reporter vector to evaluate the modulation of several growth factors. During differentiation of myoblasts into myotubes, stretched and spherical types of myoblasts were observed at 12 h after induction, at which the promoter activity began to increase. Maximal promoter activity was observed at approximately 30 h. Multinucleated myotubes were markedly formed at 72 h, but the activity was very low. IGF-I, known as a positive regulator of myogenesis, increased the promoter activity, but the increase was rather small at its high concentration (100 ng/ml). IGF-I significantly increased the level of myostatin transcript in myoblasts and newly formed myotubes at 24 h, but not at 36 h. However, the cell fusion of myoblasts was not accelerated in the presence of IGF-I. Consequently, this study indicates that the autocrine action of myostatin is partially enhanced by IGF-I through increasing its expression.
AB - Myogenesis is regulated through the proliferation and differentiation of myoblasts expressing myostatin which functions as a negative regulator by generating Smad signals. Here, we monitored the autocrine action of myostatin in quiescent chicken myoblasts transfected with the Smad-mediated promoter reporter vector to evaluate the modulation of several growth factors. During differentiation of myoblasts into myotubes, stretched and spherical types of myoblasts were observed at 12 h after induction, at which the promoter activity began to increase. Maximal promoter activity was observed at approximately 30 h. Multinucleated myotubes were markedly formed at 72 h, but the activity was very low. IGF-I, known as a positive regulator of myogenesis, increased the promoter activity, but the increase was rather small at its high concentration (100 ng/ml). IGF-I significantly increased the level of myostatin transcript in myoblasts and newly formed myotubes at 24 h, but not at 36 h. However, the cell fusion of myoblasts was not accelerated in the presence of IGF-I. Consequently, this study indicates that the autocrine action of myostatin is partially enhanced by IGF-I through increasing its expression.
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U2 - 10.1007/s11010-009-0158-6
DO - 10.1007/s11010-009-0158-6
M3 - Article
C2 - 19466527
AN - SCOPUS:74049112966
VL - 331
SP - 193
EP - 199
JO - Enzymologia
JF - Enzymologia
SN - 0300-8177
IS - 1-2
ER -