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FEBS Lett ; 500(3): 119-24, 2001 Jul 06.
Article in English | MEDLINE | ID: mdl-11445068

ABSTRACT

Insulin and leptin have overlapping effects in the control of energy homeostasis, but the molecular basis of this synergism is unknown. Insulin signals through a receptor tyrosine kinase that phosphorylates and activates the docking proteins IRSs (insulin receptor substrates), whereas the leptin receptor and its associated protein tyrosine kinase JAK2 (Janus kinase 2) mediate phosphorylation and activation of the transcription factor STAT3 (signal transducer and activator of transcription). Here, we present evidence for the integration of leptin and insulin signals in the hypothalamus. Insulin induced JAK2 tyrosine phosphorylation, leptin receptor phosphorylation which, in the presence of leptin, augmented the interaction between STAT3 and this receptor. Insulin also increased the leptin-induced phosphorylation of STAT3 and its activation. These results indicate that insulin modulates the leptin signal transduction pathway, and may provide a molecular basis for the coordinated effects of insulin and leptin in feeding behavior and weight control.


Subject(s)
DNA-Binding Proteins/metabolism , Hypothalamus/drug effects , Hypothalamus/metabolism , Insulin/administration & dosage , Leptin/administration & dosage , Proto-Oncogene Proteins , Receptors, Cell Surface , Trans-Activators/metabolism , Animals , Blotting, Western , Carrier Proteins/metabolism , Injections, Intraventricular , Janus Kinase 2 , Male , Models, Biological , Phosphorylation/drug effects , Protein-Tyrosine Kinases/metabolism , Rats , Rats, Wistar , Receptor, Insulin/metabolism , Receptors, Leptin , STAT3 Transcription Factor , Signal Transduction/drug effects
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