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
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adaptor Proteins, Signal Transducing*
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Adipose Tissue / enzymology*
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Animals
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Diet
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Enzyme Activation
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Insulin Resistance
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JNK Mitogen-Activated Protein Kinases*
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MAP Kinase Kinase 4
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Mice
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Mice, Inbred C57BL
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Mitogen-Activated Protein Kinase Kinases / metabolism*
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Nuclear Proteins / genetics
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Nuclear Proteins / metabolism*
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Trans-Activators / genetics
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Trans-Activators / metabolism*
Substances
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Adaptor Proteins, Signal Transducing
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Mapk8ip protein, mouse
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Nuclear Proteins
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Trans-Activators
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JNK Mitogen-Activated Protein Kinases
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MAP Kinase Kinase 4
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Mitogen-Activated Protein Kinase Kinases