Wnt10b inhibits obesity in ob/ob and agouti mice

被引:148
作者
Wright, Wendy S.
Longo, Kenneth A.
Dolinsky, Vernon W.
Gerin, Isabelle
Kang, Sona
Bennett, Christina N.
Chiang, Shian-Huey
Prestwich, Tyler C.
Gress, Catherine
Burant, Charles F.
Susulic, Vedrana S.
MacDougald, Ormond A.
机构
[1] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[2] Centocor Inc, Horsham, PA USA
[3] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
关键词
D O I
10.2337/db06-1339
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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/beta-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 similar to 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.
引用
收藏
页码:295 / 303
页数:9
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