Abstract
Dibutyryl cAMP (DBcAMP) inhibited insulin-like growth factor I (IGF-I)-induced DNA synthesis of rat fetal brown adipocyte primary cultures. Its mitogenic inhibitory capacity, measured as [3H]thymidine incorporation into acid-precipitable material, was dose-dependent, being maximal at 0.5 mM. The entry of cells into S + G2/M phases of the cell cycle and the increase in cell number induced by IGF-I were partially inhibited by DBcAMP at 24 h and totally prevented at 48 h. DBcAMP inhibited the mRNA expression of c-myc induced by IGF-I at 2 h. Moreover, DBcAMP inhibited in parallel H-ras mRNA expression, p21 ras, and proliferating cellular nuclear antigen protein content induced by IGF-I at 24 and 48 h of culture, respectively, suggesting the involvement of p21 ras in the progression of fetal brown adipocytes through the S phase of the cell cycle and DNA synthesis.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
1-Methyl-3-isobutylxanthine / pharmacology*
-
Adipocytes / cytology
-
Adipocytes / drug effects*
-
Adipocytes / metabolism
-
Adipose Tissue, Brown / cytology
-
Adipose Tissue, Brown / drug effects*
-
Adipose Tissue, Brown / metabolism
-
Animals
-
Bucladesine / pharmacology*
-
Cell Division / drug effects*
-
Cells, Cultured
-
Culture Media, Serum-Free
-
Cyclic AMP / metabolism*
-
Fetus
-
Gene Expression / drug effects
-
Genes, myc
-
Genes, ras
-
Insulin-Like Growth Factor I / pharmacology*
-
Kinetics
-
Proto-Oncogene Proteins c-myc / biosynthesis
-
Proto-Oncogene Proteins p21(ras) / biosynthesis
-
RNA, Messenger / analysis
-
RNA, Messenger / biosynthesis
-
Rats
-
Rats, Wistar
Substances
-
Culture Media, Serum-Free
-
Proto-Oncogene Proteins c-myc
-
RNA, Messenger
-
Bucladesine
-
Insulin-Like Growth Factor I
-
Cyclic AMP
-
Proto-Oncogene Proteins p21(ras)
-
1-Methyl-3-isobutylxanthine