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IRS1-independent defects define major nodes of insulin resistance
Authors:Hoehn Kyle L  Hohnen-Behrens Cordula  Cederberg Anna  Wu Lindsay E  Turner Nigel  Yuasa Tomoyuki  Ebina Yousuke  James David E
Affiliation:

1Diabetes and Obesity Program, Garvan Institute of Medical Research, Darlinghurst, NSW 2010, Australia

2Division of Molecular Genetics, Institute for Enzyme Research, University of Tokushima, 2-24 Shinkura-cho, Tokushima 770-8501, Japan

Abstract:Insulin resistance is a common disorder caused by a wide variety of physiological insults, some of which include poor diet, inflammation, anti-inflammatory steroids, hyperinsulinemia, and dyslipidemia. The common link between these diverse insults and insulin resistance is widely considered to involve impaired insulin signaling, particularly at the level of the insulin receptor substrate (IRS). To test this model, we utilized a heterologous system involving the platelet-derived growth factor (PDGF) pathway that recapitulates many aspects of insulin action independently of IRS. We comprehensively analyzed six models of insulin resistance in three experimental systems and consistently observed defects in both insulin and PDGF action despite a range of insult-specific defects within the IRS-Akt nexus. These findings indicate that while insulin resistance is associated with multiple deficiencies, the most deleterious defects and the origin of insulin resistance occur independently of IRS.
Keywords:HUMDISEASE   SIGNALING
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