TY - JOUR
T1 - Low-pH preparation of skeletal muscle satellite cells can be used to study activation in vitro
AU - Tatsumi, Ryuichi
AU - Yamada, Michiko
AU - Katsuki, Yoshitaka
AU - Okamoto, Shinpei
AU - Ishizaki, Junji
AU - Mizunoya, Wataru
AU - Ikeuchi, Yoshihide
AU - Hattori, Akihito
AU - Shimokawa, Hiroaki
AU - Allen, Ronald E.
N1 - Funding Information:
This work was supported in part by research grants from Ito Foundation (R.T.), and by the Arizona Agriculture Experiment Station (R.E.A.) and grants from the USDA National Research Initiative Competitive Grant Program (9504074, R.E.A.) and the Muscular Dystrophy Association (MDA3685, R.E.A.). Authors thank to Dr. N. Hashimoto, National Institute for Longevity Sciences, Japan for technical guidance for PAX7 immunocytochemistry. The mouse monoclonal anti-BrdU antibody developed by S.J. Kaufman and the anti-PAX7 antibody developed by A. Kawakami were obtained from the Developmental Studies Hybridoma Bank developed under the auspices of the NICHD and maintained by The University of Iowa, Department of Biological Sciences, Iowa City, IA 52242.
PY - 2006
Y1 - 2006
N2 - When skeletal muscle is stretched or injured, satellite cells are activated to enter the cell cycle, and this process could be mediated by hepatocyte growth factor (HGF) and nitric oxide (NO) as revealed by primary culture technique. In this system, which was originally developed by Allen et al. [Allen, R. E., Temm-Grove, C. J., Sheehan, S. M., & Rice, G. (1997). Skeletal muscle satellite cell cultures. Methods Cell Biol., 52, 155-176], however, some populations of satellite cells would receive activation signals during the cell isolation procedure; the high baseline level of activation diminishes the magnitude of the observed effect of HGF and NO. In this study, we modified the cell isolation procedure by lowering pH of muscle and isolation media from 7.2 (original) to 6.5. This modification was designed to block the activation signal generation, based on our previous observations that the satellite cell activation in response to mechanical stimulation only occurred between pH 7.1 and 7.5. Satellite cells prepared at low-pH showed a low baseline level of activation in bromodeoxyuridine incorporation and MyoD expression assays on control cultures, and demonstrated a large activation response to mechanical stretch, exogenous HGF and NO donor. Cell yield and myogenic purity were not affected by the modifications. The low-pH procedure could provide an improved satellite cell model for in vitro activation experiments.
AB - When skeletal muscle is stretched or injured, satellite cells are activated to enter the cell cycle, and this process could be mediated by hepatocyte growth factor (HGF) and nitric oxide (NO) as revealed by primary culture technique. In this system, which was originally developed by Allen et al. [Allen, R. E., Temm-Grove, C. J., Sheehan, S. M., & Rice, G. (1997). Skeletal muscle satellite cell cultures. Methods Cell Biol., 52, 155-176], however, some populations of satellite cells would receive activation signals during the cell isolation procedure; the high baseline level of activation diminishes the magnitude of the observed effect of HGF and NO. In this study, we modified the cell isolation procedure by lowering pH of muscle and isolation media from 7.2 (original) to 6.5. This modification was designed to block the activation signal generation, based on our previous observations that the satellite cell activation in response to mechanical stimulation only occurred between pH 7.1 and 7.5. Satellite cells prepared at low-pH showed a low baseline level of activation in bromodeoxyuridine incorporation and MyoD expression assays on control cultures, and demonstrated a large activation response to mechanical stretch, exogenous HGF and NO donor. Cell yield and myogenic purity were not affected by the modifications. The low-pH procedure could provide an improved satellite cell model for in vitro activation experiments.
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U2 - 10.1016/j.biocel.2006.04.003
DO - 10.1016/j.biocel.2006.04.003
M3 - Article
C2 - 16750930
AN - SCOPUS:33745393595
SN - 1357-2725
VL - 38
SP - 1678
EP - 1685
JO - International Journal of Biochemistry and Cell Biology
JF - International Journal of Biochemistry and Cell Biology
IS - 10
ER -