An essential role of the JIP1 scaffold protein for JNK activation in adipose tissue

Genes Dev. 2004 Aug 15;18(16):1976-80. doi: 10.1101/gad.1216504.

Abstract

The c-Jun NH2-terminal kinase (JNK) is activated during obesity. One consequence of obesity is that JNK phosphorylates the adapter protein insulin receptor substrate 1 (IRS-1) on Ser 307 and inhibits signaling by the insulin receptor. JNK can therefore cause peripheral insulin resistance during obesity and may contribute to the development of type 2 diabetes. Here we report that the JNK-interacting protein 1 (JIP1) scaffold protein, which binds components of the JNK signaling module, is essential for JNK activation in the adipose tissue of obese mice. These data identify JIP1 as a novel molecular target for therapeutic intervention in the development of obesity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Adipose Tissue / enzymology*
  • Animals
  • Diet
  • Enzyme Activation
  • Insulin Resistance
  • JNK Mitogen-Activated Protein Kinases*
  • MAP Kinase Kinase 4
  • Mice
  • Mice, Inbred C57BL
  • Mitogen-Activated Protein Kinase Kinases / metabolism*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*

Substances

  • Adaptor Proteins, Signal Transducing
  • Mapk8ip protein, mouse
  • Nuclear Proteins
  • Trans-Activators
  • JNK Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 4
  • Mitogen-Activated Protein Kinase Kinases