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Wnt10b Inhibits Obesity in ob/ob and Agouti Mice

机译:Wnt10b抑制ob / ob和Agouti小鼠的肥胖

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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 (A~y) 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 A~y controls, perhaps due to reduced expression and circulation of resistin. Reduced expression of inflammatory cytokines may also contribute to improved glucose homeostasis.
机译:Wnt分泌的信号分子家族对多种发育过程(包括间充质祖细胞的命运)具有深远的影响。 Wnt信号的激活会阻止脂肪形成,而Wnt10b对内源性Wnt /β-catenin信号的抑制会促进自发的前脂肪细胞分化。当维持正常饮食饮食时,具有从FABP4启动子表达Wnt10b的转基因小鼠(FABP4-Wnt10b)的脂肪组织较少,并且对饮食诱发的肥胖具有抵抗力。在这里,我们证明FABP4-Wnt10b小鼠很大程度上避免了体重增加和与遗传性肥胖相关的代谢异常。 FABP4-Wnt10b小鼠在ob / ob背景下体重没有显着增加,并且在8周龄时,与ob / ob小鼠相比,它们的内脏和皮下脂肪组织减少了约70%。同样,在致命的黄色刺豚鼠(A〜y)背景下,FABP4-Wnt10b小鼠的脂肪组织重量减少了50-70%,在5个月大时的循环瘦素减少了。 Wnt10b-Ay小鼠比Ayy对照对葡萄糖具有更高的耐受性和胰岛素敏感性,这可能是由于抵抗素的表达和循环减少所致。炎性细胞因子的表达减少也可能有助于改善葡萄糖稳态。

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