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PMID: 8960823 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Comparison of the effects of insulin, PDGF, interleukin-6, and interferon-gamma on glucose transport in 3T3-L1 cells: lack of cross-talk between tyrosine kinase receptors and JAK/STAT pathways.

Diabetologia ·Vol. 39 ·No. 12 ·1996-12-00 ·Pages 1432-9

Huppertz C, Schwartz C, Becker W, Horn F, Heinrich PC, Joost HG

Abstract

The effects of insulin, insulin-like growth factor (IGF)-I, platelet-derived growth factor (PDGF), interleukin (IL)-6 and interferon-gamma on 2-deoxyglucose uptake and insulin receptor substrate (IRS)-1 phosphorylation were compared in 3T3-L1 cells at confluence and after differentiation to the adipocyte-like phenotype. Insulin and IGF-I produced the expected stimulation of glucose transport and tyrosine phosphorylation of IRS-1 in both confluent and differentiated cells. In contrast, IL-6 and interferon-gamma failed to stimulate glucose transport or IRS-1 phosphorylation, although a marked stimulation of the JAK/STAT pathways as shown by acute-phase response factor (APRF)/Stat3 or Stat1 activation was observed in fibroblasts (IL-6, interferon-gamma) and adipocytes (IL-6). PDGF-AA and PDGF-BB stimulated glucose transport in confluent, undifferentiated cells to the same extent as insulin (approximately six-fold stimulation), but produced only a small portion of the effect of insulin in differentiated cells. Similarly, mRNA levels and autophosphorylation of PDGF receptors were much lower in differentiated cells than in confluent fibroblasts. In contrast to insulin and IGF-I, PDGF failed to stimulate tyrosine phosphorylation of IRS-1. All effects of insulin, IGF-I, and PDGF on glucose transport were inhibited by Wortmannin; the half-maximally inhibiting concentration (IC50) of Wortmannin was increased by insulin. These data demonstrate distinct signalling potentials of the investigated receptors, and indicate that the IL-6 and interferon-gamma controlled JAK/STAT pathways lack the potential to stimulate glucose transport. IRS-1 does not appear to be involved in the PDGF receptor-mediated effects, whereas activation of phosphatidylinositol (PI) 3-kinase is a crucial event in all pathways leading to stimulation of glucose transport.

MeSH Terms
3T3 Cells Animals Biological Transport/drug effects Cytokines/pharmacology DNA-Binding Proteins/drug effects,metabolism Deoxyglucose/metabolism Dose-Response Relationship, Drug Gene Expression/genetics Hypoglycemic Agents/pharmacology Insulin/pharmacology Insulin Receptor Substrate Proteins Insulin-Like Growth Factor I/pharmacology Interferon-gamma/pharmacology Interleukin-6/pharmacology Mice Nuclear Proteins/drug effects,metabolism Phosphoproteins/drug effects,metabolism Phosphorylation/drug effects Platelet-Derived Growth Factor/pharmacology Protein-Tyrosine Kinases/metabolism RNA/analysis,genetics Receptors, Platelet-Derived Growth Factor/genetics Recombinant Proteins/pharmacology STAT1 Transcription Factor STAT3 Transcription Factor Signal Transduction/drug effects,physiology Trans-Activators/drug effects,metabolism
Chemicals
Cytokines DNA-Binding Proteins Hypoglycemic Agents Insulin Insulin Receptor Substrate Proteins Interleukin-6 Irs1 protein, mouse Nuclear Proteins Phosphoproteins Platelet-Derived Growth Factor Recombinant Proteins STAT1 Transcription Factor STAT3 Transcription Factor Stat1 protein, mouse Stat3 protein, mouse Trans-Activators RNA Insulin-Like Growth Factor I Interferon-gamma Deoxyglucose Protein-Tyrosine Kinases Receptors, Platelet-Derived Growth Factor
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Huppertz C
Institut für Pharmakologie und Toxikologie, RWTH Aachen, Germany.
Schwartz C
Becker W
Horn F
Heinrich P C
Joost H G
Article Info
Journal
Diabetologia
Abbr.
Diabetologia
ISSN
0012-186X
Published
1996-12-00
Pages
1432-9
Language
English
Region
Germany
NLM ID
0006777
Subset
IM
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