HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

STAT3 sensitizes insulin signaling by negatively regulating glycogen synthase kinase-3 beta.

AbstractOBJECTIVE:
Glucose homeostasis is achieved by triggering regulation of glycogen synthesis genes in response to insulin when mammals feed, but the underlying molecular mechanism remains largely unknown. The aim of our study was to examine the role of the signal transducers and activators of transcription 3 (STAT3) in insulin signaling.
RESEARCH DESIGN AND METHODS:
We generated a strain of mice carrying a targeted disruption of Stat3 gene in the liver (L-Stat3(-/-) mice). Hepatocytes of the L-Stat3(-/-) mice were isolated to establish cell lines for mechanistic studies. Nuclear translocation and DNA-protein interaction of STAT3 was analyzed with immunofluorescent and chromatin immunoprecipitation methods, respectively. Levels of glucose, insulin, leptin, and glucagon were profiled, and putative downstream molecules of STAT3 were examined in the presence of various stimuli in L-Stat3(-/-) and control mice.
RESULTS:
STAT3 was found to sensitize the insulin signaling through suppression of GSK-3beta, a negative regulator of insulin signaling pathway. During feeding, both mRNA and protein levels of GSK-3beta decreased in Stat3(f/+) mice, which reflected the need of hepatocytes for insulin to induce glycogen synthesis. In contrast, the L-Stat3(-/-) mice lost this control and showed a monophasic increase in the GSK-3beta level in response to insulin. Administration of GSK-3beta inhibitors lithium chloride and L803-mts restored glucose homeostasis and rescued the glucose intolerance and impaired insulin response in L-Stat3(-/-) mice.
CONCLUSIONS:
These data indicate that STAT3 sensitizes insulin signaling by negatively regulating GSK-3beta. Inactivation of STAT3 in the liver contributes significantly to the pathogenesis of insulin resistance.
AuthorsAkira Moh, Wenjun Zhang, Sidney Yu, Jun Wang, Xuming Xu, Jiliang Li, Xin-Yuan Fu
JournalDiabetes (Diabetes) Vol. 57 Issue 5 Pg. 1227-35 (May 2008) ISSN: 1939-327X [Electronic] United States
PMID18268048 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Chromatin
  • Insulin
  • Prealbumin
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Glycogen Synthase Kinase 3 beta
  • Gsk3b protein, mouse
  • Glycogen Synthase Kinase 3
Topics
  • Animals
  • Cell Culture Techniques
  • Chromatin (genetics, physiology)
  • Gene Expression Regulation, Enzymologic
  • Genotype
  • Glycogen Synthase Kinase 3 (genetics)
  • Glycogen Synthase Kinase 3 beta
  • Hepatocytes (cytology, drug effects, physiology)
  • Insulin (pharmacology, physiology)
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Prealbumin (genetics)
  • STAT3 Transcription Factor (deficiency, genetics, physiology)
  • Signal Transduction (genetics, physiology)
  • Transfection

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: