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微小RNA对皮质类固醇生成基因的调控

Regulation of Corticosteroidogenic Genes by MicroRNAs.

作者信息

Robertson Stacy, Diver Louise A, Alvarez-Madrazo Samantha, Livie Craig, Ejaz Ayesha, Fraser Robert, Connell John M, MacKenzie Scott M, Davies Eleanor

机构信息

Institute of Cardiovascular and Medical Science, University of Glasgow, Glasgow, UK.

Ninewells Hospital and Medical School, University of Dundee, Dundee, UK.

出版信息

Int J Endocrinol. 2017;2017:2021903. doi: 10.1155/2017/2021903. Epub 2017 Aug 9.

Abstract

The loss of normal regulation of corticosteroid secretion is important in the development of cardiovascular disease. We previously showed that microRNAs regulate the terminal stages of corticosteroid biosynthesis. Here, we assess microRNA regulation across the whole corticosteroid pathway. Knockdown of microRNA using siRNA in H295R adrenocortical cells increased levels of , , and mRNA and the secretion of cortisol, corticosterone, 11-deoxycorticosterone, 18-hydroxycorticosterone, and aldosterone. Bioinformatic analysis of genes involved in corticosteroid biosynthesis or metabolism identified many putative microRNA-binding sites, and some were selected for further study. Manipulation of individual microRNA levels demonstrated a direct effect of miR-125a-5p and miR-125b-5p on and of miR-320a-3p levels on and mRNA. Finally, comparison of microRNA expression profiles from human aldosterone-producing adenoma and normal adrenal tissue showed levels of various microRNAs, including miR-125a-5p to be significantly different. This study demonstrates that corticosteroidogenesis is regulated at multiple points by several microRNAs and that certain of these microRNAs are differentially expressed in tumorous adrenal tissue, which may contribute to dysregulation of corticosteroid secretion. These findings provide new insights into the regulation of corticosteroid production and have implications for understanding the pathology of disease states where abnormal hormone secretion is a feature.

摘要

皮质类固醇分泌正常调节的丧失在心血管疾病的发展中具有重要意义。我们之前表明,微小RNA调节皮质类固醇生物合成的终末阶段。在此,我们评估整个皮质类固醇途径中的微小RNA调节。在H295R肾上腺皮质细胞中使用小干扰RNA敲低微小RNA可增加 、 和 信使核糖核酸水平以及皮质醇、皮质酮、11-脱氧皮质酮、18-羟皮质酮和醛固酮的分泌。对参与皮质类固醇生物合成或代谢的基因进行生物信息学分析鉴定出许多假定的微小RNA结合位点,并选择了一些进行进一步研究。对单个微小RNA水平的操作证明了miR-125a-5p和miR-125b-5p对 的直接作用以及miR-320a-3p水平对 和 信使核糖核酸的直接作用。最后,对来自人醛固酮分泌性腺瘤和正常肾上腺组织的微小RNA表达谱进行比较显示,包括miR-125a-5p在内的多种微小RNA水平存在显著差异。本研究表明,皮质类固醇生成在多个点受到几种微小RNA的调节,并且其中某些微小RNA在肿瘤性肾上腺组织中差异表达,这可能导致皮质类固醇分泌失调。这些发现为皮质类固醇产生的调节提供了新的见解,并对理解以异常激素分泌为特征的疾病状态的病理学具有启示意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7497/5568613/3b8b388f6fd1/IJE2017-2021903.001.jpg

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