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1,3,5,8-四羟基呫吨酮通过激活3T3-L1脂肪细胞中的刺猬信号通路抑制脂肪生成。

1,3,5,8-Tetrahydroxyxanthone suppressed adipogenesis via activating Hedgehog signaling in 3T3-L1 adipocytes.

作者信息

Zhou Yimeng, Kim Jin Tae, Qiu Shuai, Lee Seung Beom, Park Ho Jin, Soon Moon Jeong, Lee Hong Jin

机构信息

Department of Food Science and Biotechnology, Chung-Ang University, Anseong, 17546 South Korea.

出版信息

Food Sci Biotechnol. 2022 Jul 16;31(11):1473-1480. doi: 10.1007/s10068-022-01130-y. eCollection 2022 Oct.

Abstract

In this study, we investigated the effect of 1,3,5,8-tetrahydroxyxanthone (THX) on the adipogenesis of 3T3-L1 adipocytes. THX, a xanthone isolated from , inhibited lipid accumulation in 3T3-L1 adipocytes and reduced the protein levels of the key adipogenic transcriptional factors, peroxisome proliferator-activated receptor gamma (PPARγ) and CCAAT/enhancer-binding protein α (C/EBPα), in a dose-dependent manner. In addition, THX enhanced the transcriptional activity of Gli1 known as the key indicator of Hedgehog (Hh) signaling activity and increased the expression of Gli1 and its upstream regulator Smo. The Smo activator SAG exerted the similar effect with THX on regulating Gli1, Smo, PPARγ and C/EBPα expression, which led to the suppression of fat formation in 3T3-L1 adipocytes. Furthermore, we found that the inhibitory effect of THX on adipogenesis was derived from regulation of the early stage of adipogenesis. These results suggest that THX suppresses the differentiation of adipocyte through Hh signaling and may be considered as a potent agent for the prevention of obesity.

摘要

在本研究中,我们调查了1,3,5,8-四羟基呫吨酮(THX)对3T3-L1脂肪细胞脂肪生成的影响。THX是一种从[具体来源未给出]分离出的呫吨酮,它以剂量依赖的方式抑制3T3-L1脂肪细胞中的脂质积累,并降低关键脂肪生成转录因子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)的蛋白质水平。此外,THX增强了作为刺猬信号通路(Hh)活性关键指标的Gli1的转录活性,并增加了Gli1及其上游调节因子Smo的表达。Smo激活剂SAG在调节Gli1、Smo、PPARγ和C/EBPα表达方面与THX具有相似的作用,这导致3T3-L1脂肪细胞中脂肪形成受到抑制。此外,我们发现THX对脂肪生成的抑制作用源于对脂肪生成早期阶段的调节。这些结果表明,THX通过Hh信号通路抑制脂肪细胞分化,可能被视为预防肥胖的有效药物。

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The genetics of obesity: from discovery to biology.肥胖的遗传学:从发现到生物学。
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