Journal of Molecular Endocrinology · 1988 · 30 citations · 0 references
MedicineDevelopmental BiologyEndocrinologyGene ExpressionMetabolic RegulationTranscriptional RegulationFetal GrowthMuscle DevelopmentNeonatal GrowthSteroid Hormone SignalingSteroidogenesis RegulationAutocrine Growth SignalingDna In Situ HybridizationEndocrine Determinants Of GrowthFetal Hormonal RegulationHormonal Regulation Of GrowthPostnatal Growth RegulationRna In Situ HybridizationSkeletal Muscle Physiology
Insulin-like growth factor-II (IGF-II) is thought to be a major growth factor during fetal and neonatal development. Levels of IGF-II mRNA fall dramatically in the liver - the major site of endocrine production - between 18 and 20 days post-natally. No information concerning the control of gene expression post-natally has hitherto been available. Using Northern blotting and in-situ hybridization, we show here that cortisone acetate rapidly extinguishes IGF-II mRNA expression in the neonatal rat liver. The effect at putative autocrine/paracrine locations such as skeletal muscle and choroid plexus is much less marked or absent. The repression by cortisone acetate is discussed in the light of the available IGF-II gene sequence.