Three mitogen-activated protein kinases inhibit insulin signaling by different mechanisms in 3T3-L1 adipocytes

Mol Endocrinol. 2003 Mar;17(3):487-97. doi: 10.1210/me.2002-0131. Epub 2002 Dec 5.

Abstract

TNFalpha, which activates three different MAPKs [ERK, p38, and jun amino terminal kinase (JNK)], also induces insulin resistance. To better understand the respective roles of these three MAPK pathways in insulin signaling and their contribution to insulin resistance, constitutively active MAPK/ERK kinase (MEK)1, MAPK kinase (MKK6), and MKK7 mutants were overexpressed in 3T3-L1 adipocytes using an adenovirus-mediated transfection procedure. The MEK1 mutant, which activates ERK, markedly down-regulated expression of the insulin receptor (IR) and its major substrates, IRS-1 and IRS-2, mRNA and protein, and in turn reduced tyrosine phosphorylation of IR as well as IRS-1 and IRS-2 and their associated phosphatidyl inositol 3-kinase (PI3K) activity. The MKK6 mutant, which activates p38, moderately inhibited IRS-1 and IRS-2 expressions and IRS-1-associated PI3K activity without exerting a significant effect on the IR. Finally, the MKK7 mutant, which activates JNK, reduced tyrosine phosphorylation of IRS-1 and IRS-2 and IRS-associated PI3K activity without affecting expression of the IR, IRS-1, or IRS-2. In the context of our earlier report showing down-regulation of glucose transporter 4 by MEK1-ERK and MKK6/3-p38, the present findings suggest that chronic activation of ERK, p38, or JNK can induce insulin resistance by affecting glucose transporter expression and insulin signaling, though via distinctly different mechanisms. The contribution of ERK is, however, the strongest.

MeSH terms

  • 3T3 Cells
  • Adipocytes / enzymology*
  • Animals
  • Blotting, Western
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Gene Expression Regulation, Enzymologic / physiology
  • Glucose / metabolism
  • Insulin / physiology*
  • Insulin Receptor Substrate Proteins
  • Insulin Resistance / physiology
  • Intracellular Signaling Peptides and Proteins
  • MAP Kinase Kinase 1
  • MAP Kinase Kinase 6
  • MAP Kinase Kinase 7
  • Mice
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Mitogen-Activated Protein Kinases / metabolism*
  • Mutagenesis, Site-Directed
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoinositide-3 Kinase Inhibitors
  • Phosphoproteins / antagonists & inhibitors
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Precipitin Tests
  • Protein Serine-Threonine Kinases / metabolism
  • Signal Transduction / physiology
  • Transduction, Genetic
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Insulin
  • Insulin Receptor Substrate Proteins
  • Intracellular Signaling Peptides and Proteins
  • Irs1 protein, mouse
  • Irs2 protein, mouse
  • Phosphoinositide-3 Kinase Inhibitors
  • Phosphoproteins
  • Tumor Necrosis Factor-alpha
  • Protein Serine-Threonine Kinases
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 1
  • MAP Kinase Kinase 6
  • MAP Kinase Kinase 7
  • Map2k1 protein, mouse
  • Map2k6 protein, mouse
  • Map2k7 protein, mouse
  • Mitogen-Activated Protein Kinase Kinases
  • Glucose