4.5 Article

Activation of SOCS-3 by resistin

Journal

MOLECULAR AND CELLULAR BIOLOGY
Volume 25, Issue 4, Pages 1569-1575

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.25.4.1569-1575.2005

Keywords

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Funding

  1. NIDDK NIH HHS [P30 DK019525, P01 DK049210, R01 DK56886, R01 DK056886, P01 DK49210, DK19525, DK K01 DK59896, R01 DK49780, R01 DK049780] Funding Source: Medline

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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 similar to20 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.

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