首页> 外文期刊>Life sciences >WNT/beta-catenin pathway mediates the anti-adipogenic effect of platycodin D, a natural compound found in Platycodon grandiflorum.
【24h】

WNT/beta-catenin pathway mediates the anti-adipogenic effect of platycodin D, a natural compound found in Platycodon grandiflorum.

机译:WNT /β-catenin途径介导桔梗D(一种在桔梗中发现的天然化合物)的抗脂肪形成作用。

获取原文
获取原文并翻译 | 示例
           

摘要

AIMS: This study was conducted to suggest the role of WNT/beta-catenin pathway in the anti-adipogenic effect of platycodin D, a natural compound found in Platycodon grandiflorum. MAIN METHODS: Gene knockdown experiments using small interfering RNA (siRNA) transfection were conducted to elucidate crucial role of beta-catenin in the anti-adipogenic effects of platycodin D. Real-Time PCR and Western blot were used to analyze the expression levels of mRNAs and proteins in the WNT/beta-catenin pathway. KEY FINDINGS: During the adipocyte differentiation of 3 T3-L1 cells, members of the WNT/beta-catenin pathway were normally down-regulated, whereas platycodin D significantly reinstated the WNT/beta-catenin pathway. The mRNA and protein expressions of disheveled (DVL) 2, which stabilize beta-catenin, were increased by platycodin D treatment, but the protein level of AXIN, which induces the degradation of beta-catenin, was decreased in platycodin D-treated cells. The nuclear level of beta-catenin was normally down-regulated during adipogenesis, but platycodin D treatment led to the accumulation of beta-catenin in the nucleus which resulted in the up-regulation of its target genes, cyclin D (CCND) 1 and peroxisome proliferator-activated receptor gamma (PPAR)gamma. The anti-adipogenic effects of platycodin D were significantly attenuated in beta-catenin siRNA-transfected cells compared with those of control siRNA-transfected cells. beta-catenin siRNA transfection significantly recovered the levels of PPARgamma, CCAAT/enhancer binding protein (C/EBP)alpha and fatty acid binding protein (FABP)4 as well as intracellular lipid droplet formation, all of which were reduced by platycodin D treatment. SIGNIFICANCE: WNT/beta-catenin pathway can be used as a therapeutic target of natural compounds for the regulation of adipogenesis.
机译:目的:进行这项研究以表明WNT /β-catenin途径在桔梗D(一种在桔梗中发现的天然化合物)的抗脂肪形成作用中的作用。主要方法:使用小干扰RNA(siRNA)转染进行基因敲低实验,以阐明β-连环蛋白在铂类抗D素的抗脂肪形成作用中的关键作用。采用实时PCR和Western印迹分析mRNA的表达水平和WNT /β-catenin途径中的蛋白质。主要发现:在3个T3-L1细胞的脂肪细胞分化过程中,WNT /β-catenin通路的成员通常被下调,而铂霉素D显着恢复了WNT /β-catenin通路。稳定β-catenin的不整齐(DVL)2的mRNA和蛋白表达通过铂霉素D处理而增加,但是诱导β-catenin降解的AXIN蛋白水平在铂霉素D处理的细胞中降低了。 β-catenin的核水平通常在脂肪形成过程中被下调,但是铂类D处理导致β-catenin在细胞核中积累,从而导致其靶基因cyclin D(CCND)1和过氧化物酶体上调。增殖物激活受体γ(PPAR)γ。与对照siRNA转染的细胞相比,β-cateninsiRNA转染的细胞中platycodin D的抗脂肪形成作用显着减弱。 β-cateninsiRNA转染可显着恢复PPARgamma,CCAAT /增强子结合蛋白(C / EBP)α和脂肪酸结合蛋白(FABP)4的水平,以及细胞内脂质小滴的形成,所有这些都可通过platycodin D处理降低。意义:WNT /β-catenin途径可作为天然化合物的治疗靶标,用于调节脂肪形成。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号