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过氧化物酶体增殖物激活受体α(PPARα)在人肝脏中受 miR-21 和 miR-27b 的调控。

PPARα is regulated by miR-21 and miR-27b in human liver.

机构信息

Drug Metabolism and Toxicology, Faculty of Pharmaceutical Sciences, Kanazawa University, Kakuma-machi, Kanazawa, 920-1192, Japan.

出版信息

Pharm Res. 2011 Oct;28(10):2467-76. doi: 10.1007/s11095-011-0473-y. Epub 2011 May 12.

Abstract

PURPOSE

Peroxisome proliferator-activated receptor α (PPARα) is an important transcriptional factor that regulates genes encoding endo/xenobiotic enzymes and lipid metabolizing enzymes. In this study, we investigated whether microRNAs (miRNAs) are involved in the regulation of PPARα in human liver.

METHODS

Precursor or antisense oligonucleotide for miR-21 or miR-27b was transfected into HuH7 cells; expression of PPARα and acyl-CoA synthetase M2B was determined by Western blot and real-time RT-PCR. Luciferase assay was performed to identify the functional miRNA recognition element (MRE). Expression levels of PPARα, miR-21, and miR-27b in a panel of 24 human livers were determined.

RESULTS

The overexpression and inhibition of miR-21 or miR-27b in HuH7 cells significantly decreased and increased the PPARα protein level, respectively, but not PPARα mRNA level. The miRNA-dependent regulation of PPARα affected the expression of its downstream gene. Luciferase assay identified a functional MRE for miR-21 in the 3'-untranslated region of PPARα. In human livers, the PPARα protein levels were not correlated with PPARα mRNA, but inversely correlated with the miR-21 levels, suggesting a substantial impact of miR-21, although the contribution of miR-27b could not be ruled out.

CONCLUSIONS

We found that PPARα in human liver is regulated by miRNAs.

摘要

目的

过氧化物酶体增殖物激活受体α(PPARα)是一种重要的转录因子,可调节编码内源性/外源性酶和脂质代谢酶的基因。本研究旨在探讨微小 RNA(miRNA)是否参与人类肝脏中 PPARα的调控。

方法

将 miR-21 或 miR-27b 的前体或反义寡核苷酸转染入 HuH7 细胞;通过 Western blot 和实时 RT-PCR 测定 PPARα 和酰基辅酶 A 合成酶 M2B 的表达。通过荧光素酶测定鉴定功能性 miRNA 识别元件(MRE)。测定 24 个人肝组织样本中 PPARα、miR-21 和 miR-27b 的表达水平。

结果

HuH7 细胞中 miR-21 或 miR-27b 的过表达和抑制分别显著降低和增加了 PPARα 蛋白水平,但不影响 PPARα mRNA 水平。miRNA 对 PPARα 的调控影响了其下游基因的表达。荧光素酶测定鉴定出 PPARα 3'非翻译区中 miR-21 的功能性 MRE。在人肝组织中,PPARα 蛋白水平与 PPARα mRNA 无相关性,而与 miR-21 水平呈负相关,提示 miR-21 具有显著影响,尽管不能排除 miR-27b 的作用。

结论

我们发现人类肝脏中的 PPARα 受 miRNA 调控。

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