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潜在的miRNA参与白藜芦醇及其代谢产物的抗脂肪生成作用。

Potential miRNA involvement in the anti-adipogenic effect of resveratrol and its metabolites.

作者信息

Eseberri Itziar, Lasa Arrate, Miranda Jonatan, Gracia Ana, Portillo Maria P

机构信息

Nutrition and Obesity group, Department of Nutrition and Food Science, University of Basque Country (UPV/EHU) and Lucio Lascaray Research Center, Vitoria, Spain.

Centro de Investigación Biomédica en Fisiopatología de la Obesidad y Nutrición (CIBERobn), Instituto de Salud Carlos III, Madrid, Spain.

出版信息

PLoS One. 2017 Sep 27;12(9):e0184875. doi: 10.1371/journal.pone.0184875. eCollection 2017.

Abstract

OBJECTIVE

Scientific research is constantly striving to find molecules which are effective against excessive body fat and its associated complications. Taking into account the beneficial effects that resveratrol exerts on other pathologies through miRNA, the aim of the present work was to analyze the possible involvement of miRNAs in the regulation of adipogenic transcription factors peroxisome proliferator-activated receptor γ (pparγ), CCAAT enhancer-binding proteins α and β (cebpβ and cebpα) induced by resveratrol and its metabolites.

METHODS

3T3-L1 maturing pre-adipocytes were treated during differentiation with 25 μM of trans-resveratrol (RSV), trans-resveratrol-3-O-sulfate (3S), trans-resveratrol-3'-O-glucuronide (3G) and trans-resveratrol-4'-O-glucuronide (4G). After computational prediction and bibliographic search of miRNAs targeting pparγ, cebpβ and cebpα, the expression of microRNA-130b-3p (miR-130b-3p), microRNA-155-5p (miR-155-5p), microRNA-27b-3p (miR-27b-3p), microRNA-31-5p (miR-31-5p), microRNA-326-3p (miR-326-3p), microRNA-27a-3p (miR-27a-3p), microRNA-144-3p (miR-144-3p), microRNA-205-5p (miR-205-5p) and microRNA-224-3p (miR-224-3p) was analyzed. Moreover, other adipogenic mediators such as sterol regulatory element binding transcription factor 1 (srebf1), krüppel-like factor 5 (klf5), liver x receptor α (lxrα) and cAMP responding element binding protein 1 (creb1), were measured by Real Time RT-PCR. As a confirmatory assay, cells treated with RSV were transfected with anti-miR-155 in order to measure cebpβ gene and protein expressions.

RESULTS

Of the miRNAs analyzed only miR-155 was modified after resveratrol and glucuronide metabolite treatment. In transfected cells with anti-miR-155, RSV did not reduce cebpβ gene and protein expression. 3S decreased gene expression of creb1, klf5, srebf1 and lxrα.

CONCLUSIONS

While RSV and glucuronide metabolites exert their inhibitory effect on adipogenesis through miR-155 up-regulation, the anti-adipogenic effect of 3S is not mediated via miRNAs.

摘要

目的

科学研究一直在努力寻找对过多体脂及其相关并发症有效的分子。考虑到白藜芦醇通过微小RNA(miRNA)对其他病理状况产生的有益作用,本研究的目的是分析miRNA在白藜芦醇及其代谢产物诱导的脂肪生成转录因子过氧化物酶体增殖物激活受体γ(pparγ)、CCAAT增强子结合蛋白α和β(cebpβ和cebpα)调控中的可能作用。

方法

在3T3-L1成熟前脂肪细胞分化过程中,用25μM反式白藜芦醇(RSV)、反式白藜芦醇-3-O-硫酸盐(3S)、反式白藜芦醇-3'-O-葡萄糖醛酸苷(3G)和反式白藜芦醇-4'-O-葡萄糖醛酸苷(4G)进行处理。在对靶向pparγ、cebpβ和cebpα的miRNA进行计算预测和文献检索后,分析微小RNA-130b-3p(miR-130b-3p)、微小RNA-155-5p(miR-155-5p)、微小RNA-27b-3p(miR-27b-3p)、微小RNA-31-5p(miR-31-5p)、微小RNA-326-3p(miR-326-3p)、微小RNA-27a-3p(miR-27a-3p)、微小RNA-144-3p(miR-144-3p)、微小RNA-205-5p(miR-205-5p)和微小RNA-224-3p(miR-224-3p)的表达。此外,通过实时逆转录聚合酶链反应(Real Time RT-PCR)检测其他脂肪生成介质,如固醇调节元件结合转录因子1(srebf1)、克鲁ppel样因子5(klf5)、肝脏X受体α(lxrα)和cAMP反应元件结合蛋白1(creb1)。作为验证试验,用抗miR-155转染经RSV处理的细胞,以检测cebpβ基因和蛋白表达。

结果

在所分析的miRNA中,只有miR-155在白藜芦醇和葡萄糖醛酸苷代谢产物处理后发生了改变。在转染了抗miR-155的细胞中,RSV并未降低cebpβ基因和蛋白表达。3S降低了creb1、klf5、srebf1和lxrα的基因表达。

结论

虽然RSV和葡萄糖醛酸苷代谢产物通过上调miR-155对脂肪生成发挥抑制作用,但3S的抗脂肪生成作用不是通过miRNA介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b700/5617156/9b54488e7c42/pone.0184875.g001.jpg

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