Growth hormone (GH)-stimulated insulin-like growth factor I gene expression is mediated by a tyrosine phosphorylation pathway depending on C-terminal region of human GH receptor in human GH receptor-expressing Ba/F3 cells

Endocrinology. 2004 Jan;145(1):214-20. doi: 10.1210/en.2003-0811. Epub 2003 Oct 9.

Abstract

The signaling pathway of GH-stimulated IGF-I gene expression is still unclear, although it has been reported that the Janus kinase (JAK)-signal transducers and activators of transcription (STAT)5b pathway plays an important role in liver IGF-I expression. In this study, the GH-dependent IGF-I gene expression and its intracellular signaling mechanism have been examined in mouse pro-B, Ba/F3 cells stably expressing human GH receptor (Ba/F3-hGHR). The IGF-I gene expression was stimulated by human GH (0.01-10 nm) in a dose-dependent fashion in Ba/F3-hGHR cells. The specific inhibitors for JAK2 remarkably suppressed the GH-induced IGF-I gene expression, but MAPK or phosphatidylinositol 3 kinase-specific inhibitors failed to block the GH stimulation of the IGF-I gene expression. However, genistein, a nonspecific tyrosine kinase inhibitor that does not inhibit JAK2 and STAT5 phosphorylation, significantly suppressed the GH-induced IGF-I gene expression. Additionally, a Ba/F3-hGHR mutant that contained the truncated C-terminal hGHR up to D351 showed no IGF-I gene expression in response to human GH. The D351 form normally has the GH-induced JAK/STAT5 tyrosine phosphorylation. These results suggest that the JAK-STAT5 pathway and the novel tyrosine phosphorylation pathway, dependent on signaling from the C-terminal region of hGHR, might be involved in the GH-stimulated IGF-I gene expression in Ba/F3 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Cycloheximide / pharmacology
  • DNA-Binding Proteins / metabolism
  • Gene Expression / drug effects
  • Growth Hormone / pharmacology*
  • Humans
  • Insulin-Like Growth Factor I / genetics*
  • Janus Kinase 2
  • Mice
  • Milk Proteins*
  • Mitogen-Activated Protein Kinases / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphorylation / drug effects
  • Protein Structure, Tertiary
  • Protein Synthesis Inhibitors / pharmacology
  • Protein-Tyrosine Kinases / metabolism
  • Proto-Oncogene Proteins*
  • RNA, Messenger / analysis
  • Receptors, Somatotropin / chemistry
  • Receptors, Somatotropin / genetics*
  • Receptors, Somatotropin / metabolism*
  • STAT5 Transcription Factor
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Trans-Activators / metabolism
  • Tyrosine / metabolism

Substances

  • DNA-Binding Proteins
  • Milk Proteins
  • Protein Synthesis Inhibitors
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Receptors, Somatotropin
  • STAT5 Transcription Factor
  • Trans-Activators
  • Tyrosine
  • Insulin-Like Growth Factor I
  • Growth Hormone
  • Cycloheximide
  • Phosphatidylinositol 3-Kinases
  • Protein-Tyrosine Kinases
  • JAK2 protein, human
  • Jak2 protein, mouse
  • Janus Kinase 2
  • Mitogen-Activated Protein Kinases