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2007 Fiscal Year Final Research Report Summary

Regulation of energy metabolism by the insulin receptor substrate Dok-1

Research Project

Project/Area Number 18590989
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Metabolomics
Research InstitutionKobe University

Principal Investigator

NOGUCHI Tetsuya  Kobe University, Graduate School of Medicine, Assistant Professor (10372640)

Project Period (FY) 2006 – 2007
KeywordsInsulin receptor substrate / adipocyte / obesity
Research Abstract

Insulin receptor substrate (IRS)-1 and IRS-2 have dominant roles in the action of insulin, but other substrates of the insulin receptor kinase, such as Gab1, c-Cb1, SH2-B and APS, are also of physiological relevance. Although the protein downstream of tyrosine kinases-1 (Dok1) is known to function as a multisite adapter molecule in insulin signaling, its role in energy homeostasis has remained unclear. Here we show that Dok1 regulates adiposity. Expression of Dok1 in white adipose tissue was markedly increased in mice fed a high-fat diet, whereas adipocytes lacking this adapter were smaller and showed a reduced hypertrophic response to this dietary manipulation. Dok1-deficient mice were leaner and showed improved glucose tolerance and insulin sensitivity compared with wild-type mice. Embryonic fibroblasts from Dok1-deficient mice were impaired in adipogenic differentiation, and this defect was accompanied by an increased activity of the protein kinase ERK and a consequent increase in the phosphorylation of peroxisome proliferator-activated receptor (PPAR) -gamma on Ser 112. Mutation of this negative regulatory site for the transactivation activity of PPAR-gamma blocked development of the lean phenotype caused by Dok1 ablation. These results indicate that Dok1 promotes adipocyte hypertrophy by counteracting the inhibitory effect of ERK on PPAR-gamma and may thus confer predisposition to diet-induced obesity.

  • Research Products

    (4 results)

All 2008 2007

All Journal Article (2 results) (of which Peer Reviewed: 1 results) Presentation (2 results)

  • [Journal Article] Dok-1 mediates high-fat diet-induced adipocyte hypertrophy and obesity through modulation of PPAR-γ phosphorylation2008

    • Author(s)
      Hosooka T., et. al.
    • Journal Title

      Nature Medicine 14

      Pages: 188-193

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
  • [Journal Article] Dok-1 mediates high-fat diet-induced adipocyte hypertrophy and obesity through modulation of PPAR-γ phosphorylation2008

    • Author(s)
      Hosooka, T., Noguchi, T., Kotani, K., Nakamura, T., Sakaue, H., Inoue, H., Ogawa, W., Tobimatsu, K., Takazawa, K., Sakai, M., Matsuki, Y., Hiramatsu, R., Yasuda, T., Lazar, MA., Yamanashi, Y., Kasuga, M
    • Journal Title

      Nature Medicine Vol. 14

      Pages: 188-193

    • Description
      「研究成果報告書概要(欧文)」より
  • [Presentation] Dok-1はPPARγの活性調節を介して肥満およびインスリン抵抗性の発症に関与する2007

    • Author(s)
      細岡哲也, 他9名
    • Organizer
      第50回日本糖尿病学会年次学術集会
    • Place of Presentation
      仙台
    • Year and Date
      2007-05-25
    • Description
      「研究成果報告書概要(和文)」より
  • [Presentation] Dok-1 mediates high-fat diet-induced obesity and Insulin resistance through modulation of PPAR-γ phosphorylation2007

    • Author(s)
      Hosooka, T., et. al.
    • Organizer
      50th Annual Meeting of the Japan Diabetes Society
    • Place of Presentation
      Sendai, Japan
    • Year and Date
      2007-05-25
    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2010-02-04  

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