Activation of SOCS-3 by Resistin
Activation of SOCS-3 by Resistin
Resistin is an adipocyte hormone that modulates glucose homeostasis. Here we show that in 3T3-L1 adipocytes, resistin attenuates multiple effects of insulin, including insulin receptor (IR) phosphorylation, IR substrate 1 (IRS-1) phosphorylation, phosphatidylinositol-3-kinase (PI3K) activation, phosphatidylinositol triphosphate production, and activation of protein kinase B/Akt. Remarkably, resistin treatment markedly induces the gene expression of suppressor of cytokine signaling 3 (SOCS-3), a known inhibitor of insulin signaling. The 50% effective dose for resistin induction of SOCS-3 is approximately 20 ng/ml, close to levels of resistin in serum. Association of SOCS-3 protein with the IR is also increased by resistin. Inhibition of SOCS function prevented resistin from antagonizing insulin action in adipocytes. SOCS-3 induction is the first cellular effect of resistin that is independent of insulin and is a likely mediator of resistin's inhibitory effect on insulin signaling in adipocytes.
- University of Pennsylvania United States
- Howard Hughes Medical Institute United States
- Pfizer (United States) United States
Cell Differentiation, Protein Serine-Threonine Kinases, Phosphoproteins, Receptor, Insulin, Enzyme Activation, Repressor Proteins, Mice, Phosphatidylinositol 3-Kinases, 3T3-L1 Cells, Proto-Oncogene Proteins, Hormones, Ectopic, Adipocytes, Insulin Receptor Substrate Proteins, Animals, Insulin, Resistin, Insulin Resistance, Phosphorylation, Proto-Oncogene Proteins c-akt, Cells, Cultured
Cell Differentiation, Protein Serine-Threonine Kinases, Phosphoproteins, Receptor, Insulin, Enzyme Activation, Repressor Proteins, Mice, Phosphatidylinositol 3-Kinases, 3T3-L1 Cells, Proto-Oncogene Proteins, Hormones, Ectopic, Adipocytes, Insulin Receptor Substrate Proteins, Animals, Insulin, Resistin, Insulin Resistance, Phosphorylation, Proto-Oncogene Proteins c-akt, Cells, Cultured
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