Differentially expressed microRNAs in the corpus cavernosum from a murine model with type 2 diabetes mellitus-associated erectile dysfunction

被引:0
作者
Feng Pan
Jinwei You
Yuan Liu
Xuefeng Qiu
Wen Yu
Jiehua Ma
Lianjun Pan
Aixia Zhang
Qipeng Zhang
机构
[1] Maternity Hospital Affiliated to Nanjing Medical University,State Key Laboratory of Reproductive Medicine, Department of Andrology
[2] Nanjing University,Department of Comparative Medicine, Jinling Hospital, School of Clinical Medicine
[3] Nanjing University,State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Jiangsu Engineering Research Center for microRNA Biology and Biotechnology
[4] Nanjing University,Department of Andrology, Affiliated Drum Tower Hospital, School of Medicine
来源
Molecular Genetics and Genomics | 2016年 / 291卷
关键词
MicroRNA; Erectile dysfunction; Diabetes mellitus; Array analysis; Endothelium; Smooth muscle;
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学科分类号
摘要
To better understand the molecular aetiology of type 2 diabetes mellitus-associated erectile dysfunction (T2DMED) and to provide candidates for further study of its diagnosis and treatment, this study was designed to investigate differentially expressed microRNAs (miRNAs) in the corpus cavernosum (CC) of mice with T2DMED using GeneChip array techniques (Affymetrix miRNA 4.0 Array) and to predict target genes and signalling pathways regulated by these miRNAs based on bioinformatic analysis using TargetScan, the DAIAN web platform and DAVID. In the initial screening, 21 miRNAs appeared distinctly expressed in the T2DMED group (fold change ≥3, p ≤ 0.01). Among them, the differential expression of miR-18a, miR-206, miR-122, and miR-133 were confirmed by qRT-PCR (p < 0.05 and FDR <5 %). According to bioinformatic analysis, the four miRNAs were speculated to play potential roles in the mechanisms of T2DMED via regulating 28 different genes and several pathways, including apoptosis, fibrosis, eNOS/cGMP/PKG, and vascular smooth muscle contraction processes, which mainly focused on influencing the functions of the endothelium and smooth muscle in the CC. IGF-1, as one of the target genes, was verified to decrease in the CCs of T2DMED animals via ELISA and was confirmed as the target of miR-18a or miR-206 via luciferase assay. Finally, these four miRNAs deserve further confirmation as biomarkers of T2DMED in larger studies. Additionally, miR-18a and/or miR-206 may provide new preventive/therapeutic targets for ED management by targeting IGF-1.
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页码:2215 / 2224
页数:9
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