Drug Metabolism and Toxicology, Faculty of Pharmaceutical Sciences, Kanazawa University, Kakuma-machi, Kanazawa, 920-1192, Japan.
Pharm Res. 2011 Oct;28(10):2467-76. doi: 10.1007/s11095-011-0473-y. Epub 2011 May 12.
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.
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.
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.
We found that PPARα in human liver is regulated by miRNAs.
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。
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。
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。
我们发现人类肝脏中的 PPARα 受 miRNA 调控。