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Wnt/β-连环蛋白信号通路参与了幼体大菱鲆(Scophthalmus maximus L.)肝脏中脂肪生成的调控。

Wnt/β-catenin signaling participates in the regulation of lipogenesis in the liver of juvenile turbot (Scophthalmus maximus L.).

作者信息

Liu Dongwu, Mai Kangsen, Zhang Yanjiao, Xu Wei, Ai Qinghui

机构信息

Key Laboratory of Aquaculture Nutrition and Feed (Ministry of Agriculture), Ocean University of China, Qingdao 266003, PR China; Key Laboratory of Mariculture (Education Ministry of China), Ocean University of China, Qingdao 266003, PR China.

Key Laboratory of Aquaculture Nutrition and Feed (Ministry of Agriculture), Ocean University of China, Qingdao 266003, PR China; Key Laboratory of Mariculture (Education Ministry of China), Ocean University of China, Qingdao 266003, PR China.

出版信息

Comp Biochem Physiol B Biochem Mol Biol. 2016 Jan;191:155-62. doi: 10.1016/j.cbpb.2015.11.002. Epub 2015 Nov 3.

Abstract

In this study, the mechanism that Wnt/β-catenin signaling inhibits lipogenesis was investigated in the liver of juvenile turbot (Scophthalmus maximus L.) by LiCl or XAV939 treatment. Wnt/β-catenin signaling was activated by LiCl treatment or inhibited by XAV939 treatment through regulating the expression of glycogen synthase kinase-3β (GSK-3β) and Wnt10b. In addition, the expression of lipoprotein lipase (LPL), fatty acid synthetase (FAS), peroxisome proliferator-activated receptor γ (PPARγ), and CCAAT/enhancer binding protein α (C/EBPα) was inhibited by LiCl treatment, but induced by XAV939 treatment. In the plasma of juvenile turbot, the level of nonesterified fatty acid (NEFA), glycerol, triglyceride (TG), total cholesterol (TC), and low density lipoprotein cholesterol (LDL-C) was decreased by LiCl treatment, which was related to the decrease of the activity of LPL and FAS. Thus the inhibitory effect of Wnt/β-catenin signaling on lipogenesis was associated with the expression of key enzymes and transcriptional factors. Wnt/β-catenin signaling may participate in inhibiting lipogenesis by inhibiting the expression of PPARγ and C/EBPα in the liver of juvenile turbot.

摘要

在本研究中,通过氯化锂(LiCl)或XAV939处理,在幼体大菱鲆(Scophthalmus maximus L.)肝脏中研究了Wnt/β-连环蛋白信号通路抑制脂肪生成的机制。通过调节糖原合酶激酶-3β(GSK-3β)和Wnt10b的表达,LiCl处理激活Wnt/β-连环蛋白信号通路,而XAV939处理抑制该信号通路。此外,LiCl处理抑制脂蛋白脂肪酶(LPL)、脂肪酸合成酶(FAS)、过氧化物酶体增殖物激活受体γ(PPARγ)和CCAAT/增强子结合蛋白α(C/EBPα)的表达,但XAV939处理诱导这些蛋白的表达。在幼体大菱鲆血浆中,LiCl处理使非酯化脂肪酸(NEFA)、甘油、甘油三酯(TG)、总胆固醇(TC)和低密度脂蛋白胆固醇(LDL-C)水平降低,这与LPL和FAS活性降低有关。因此,Wnt/β-连环蛋白信号通路对脂肪生成的抑制作用与关键酶和转录因子的表达有关。Wnt/β-连环蛋白信号通路可能通过抑制幼体大菱鲆肝脏中PPARγ和C/EBPα的表达参与抑制脂肪生成。

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