TY - JOUR
T1 - Satellite cell myogenesis is highly stimulated by the kinase inhibitor iso-H7
T2 - Comparison with HA1004 and staurosporine effects
AU - Lagord, Catherine
AU - Carpentier, Gilles
AU - Moraczewski, Jerzy
AU - Pons, Gabriel
AU - Climent, Fernando
AU - Martelly, Isabelle
PY - 1993/3/31
Y1 - 1993/3/31
N2 - Differentiation of rat satellite cells, measured by cell fusion into myotubes and isozymic conversion of creatine kinase and phosphoglycerate mutase, was shown to be highly increased in the presence of 1-(5- isoquinolinylsulfonyl)-3-methylpiperazine (iso-H7). This substance inhibited both protein kinase C (PKC) and cAMP-dependent protein kinase (PKA) activities with similar IC50 between 22 and 34 μM. Iso-H7, as well as the PKA inhibitor HA1004 increased myogenic differentiation without altering the proliferation of satellite cells, whereas the proliferation and the differentiation of these cells were inhibited by the PKC inhibitor staurosporine. Our results suggest a predominant negative control of PKA on satellite cell myogenesis.
AB - Differentiation of rat satellite cells, measured by cell fusion into myotubes and isozymic conversion of creatine kinase and phosphoglycerate mutase, was shown to be highly increased in the presence of 1-(5- isoquinolinylsulfonyl)-3-methylpiperazine (iso-H7). This substance inhibited both protein kinase C (PKC) and cAMP-dependent protein kinase (PKA) activities with similar IC50 between 22 and 34 μM. Iso-H7, as well as the PKA inhibitor HA1004 increased myogenic differentiation without altering the proliferation of satellite cells, whereas the proliferation and the differentiation of these cells were inhibited by the PKC inhibitor staurosporine. Our results suggest a predominant negative control of PKA on satellite cell myogenesis.
UR - http://www.scopus.com/inward/record.url?scp=0027221066&partnerID=8YFLogxK
U2 - 10.1006/bbrc.1993.1306
DO - 10.1006/bbrc.1993.1306
M3 - Article
AN - SCOPUS:0027221066
SN - 0006-291X
VL - 191
SP - 928
EP - 936
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -