Wnt10b Inhibits Obesity in ob/ob and Agouti Mice

  1. Wendy S. Wright1,
  2. Kenneth A. Longo1,
  3. Vernon W. Dolinsky1,
  4. Isabelle Gerin1,
  5. Sona Kang1,
  6. Christina N. Bennett1,
  7. Shian-Huey Chiang1,
  8. Tyler C. Prestwich1,
  9. Catherine Gress2,
  10. Charles F. Burant13,
  11. Vedrana S. Susulic2 and
  12. Ormond A. MacDougald13
  1. 1Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan
  2. 2Centocor, Horsham, Pennsylvania
  3. 3Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan
  1. Address correspondence and reprint requests to Ormond A. MacDougald, Department of Molecular and Integrative Physiology, 7620 Medical Science II, 1301 E. Catherine Dr., Ann Arbor, MI 48109-0622. E-mail: macdouga{at}umich.edu

Abstract

The Wnt family of secreted signaling molecules has profound effects on diverse developmental processes, including the fate of mesenchymal progenitors. While activation of Wnt signaling blocks adipogenesis, inhibition of endogenous Wnt/β-catenin signaling by Wnt10b promotes spontaneous preadipocyte differentiation. Transgenic mice with expression of Wnt10b from the FABP4 promoter (FABP4-Wnt10b) have less adipose tissue when maintained on a normal chow diet and are resistant to diet-induced obesity. Here we demonstrate that FABP4-Wnt10b mice largely avert weight gain and metabolic abnormalities associated with genetic obesity. FABP4-Wnt10b mice do not gain significant body weight on the ob/ob background, and at 8 weeks of age, they have an ∼70% reduction in visceral and subcutaneous adipose tissues compared with ob/ob mice. Similarly, on the lethal yellow agouti (Ay) background, FABP4-Wnt10b mice have 50–70% less adipose tissue weight and circulating leptin at 5 months of age. Wnt10b-Ay mice are more glucose tolerant and insulin sensitive than Ay controls, perhaps due to reduced expression and circulation of resistin. Reduced expression of inflammatory cytokines may also contribute to improved glucose homeostasis.

Footnotes

  • W.S.W. and K.A.L. contributed equally to this work.

  • The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    • Accepted November 1, 2006.
    • Received September 25, 2006.
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