Centre for Neuroendocrinology and Brain Health Research Centre, University Otago, Dunedin, New Zealand.
Department of Physiology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
FASEB J. 2022 Mar;36(3):e22207. doi: 10.1096/fj.202101764R.
Leptin is best known for its role in adipostasis, but it also regulates blood glucose levels. The molecular mechanism by which leptin controls glucose homeostasis remains largely unknown. Here, we use a zebrafish model to show that Wnt signaling mediates the glucoregulatory effects of leptin. Under normal feeding conditions, leptin regulates glucose homeostasis but not adipostasis in zebrafish. In times of nutrient excess, however, we found that leptin also regulates body weight and size. Using a Wnt signaling reporter fish, we show that leptin activates the canonical Wnt pathway in vivo. Utilizing two paradigms for hyperglycemia, it is revealed that leptin regulates glucose homeostasis via the Wnt pathway, as pharmacological inhibition of this pathway impairs the glucoregulatory actions of leptin. Our results may shed new light on the evolution of the physiological function of leptin.
瘦素以其在脂肪生成中的作用而闻名,但它也能调节血糖水平。瘦素控制血糖稳态的分子机制在很大程度上尚不清楚。在这里,我们使用斑马鱼模型表明 Wnt 信号介导了瘦素的葡萄糖调节作用。在正常喂养条件下,瘦素调节斑马鱼的血糖稳态,但不调节脂肪生成。然而,在营养过剩时,我们发现瘦素也调节体重和体型。使用 Wnt 信号报告鱼,我们表明瘦素在体内激活经典的 Wnt 途径。利用两种高血糖症范式,揭示了瘦素通过 Wnt 途径调节血糖稳态,因为该途径的药理学抑制会损害瘦素的葡萄糖调节作用。我们的结果可能为瘦素生理功能的进化提供新的线索。