Integrated miRNA and mRNA expression profiling in inflamed colon of patients with ulcerative colitis

• Published in: PloS one 2014-12, Vol.9 (12), p.e116117-e116117
• Main Authors: Van der Goten, Jan, Vanhove, Wiebe, Lemaire, Katleen, Van Lommel, Leentje, Machiels, Kathleen, Wollants, Willem-Jan, De Preter, Vicky, De Hertogh, Gert, Ferrante, Marc, Van Assche, Gert, Rutgeerts, Paul, Schuit, Frans, Vermeire, Séverine, Arijs, Ingrid
• Format: Article
• Language: English
• Subjects: Active control; Analysis; Base Sequence; Binding sites; Biology and life sciences; Biopsy; Breast cancer; Cadherins - genetics; Cadherins - metabolism; Case-Control Studies; Cell adhesion & migration; Chromosome 3; Colitis, Ulcerative - complications; Colitis, Ulcerative - genetics; Colitis, Ulcerative - pathology; Colon; Colon - metabolism; Colon - pathology; Correlation; Correlation analysis; Crohn's disease; Crohns disease; DNA microarrays; Endoscopy; Epithelial Cells - metabolism; Female; Gene expression; Gene Expression Profiling; Gene Expression Regulation; Genes; Genes, Reporter; Genomes; HT29 Cells; Humans; Immune response; Immune system; Inflammation; Inflammation - complications; Inflammation - genetics; Inflammation - pathology; Inflammatory bowel disease; Inflammatory bowel diseases; Interleukin 8; Interleukin-8 - genetics; Interleukin-8 - metabolism; Intestinal Mucosa - metabolism; Intestinal Mucosa - pathology; Intestine; Luciferases - metabolism; Male; Medicine; Medicine and Health Sciences; Messenger RNA; MicroRNA; MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; Middle Aged; miRNA; Molecular Sequence Data; Mucosa; Oligonucleotide Array Sequence Analysis; Pathogenesis; Patients; Profiling; Real-Time Polymerase Chain Reaction; Regulators; Reproducibility of Results; Research and Analysis Methods; Ribonucleic acid; RNA; RNA, Messenger - genetics; RNA, Messenger - metabolism; Target recognition; Ulcerative colitis
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0116117

Ulcerative colitis (UC) is associated with differential colonic expression of genes involved in immune response (e.g. IL8) and barrier integrity (e.g. cadherins). MicroRNAs (miRNAs) are regulators of gene expression and are involved in various immune-related diseases. In this study, we investigated (1) if miRNA expression in UC mucosa is altered and (2) if any of these changes correlate with mucosal mRNA expression. Integration of mRNA and miRNA expression profiling may allow the identification of functional links between dysregulated miRNAs and their target mRNA. Colonic mucosal biopsies were obtained from 17 UC (10 active and 7 inactive) patients and 10 normal controls. Total RNA was used to analyze miRNA and mRNA expression via Affymetrix miRNA 2.0 and Affymetrix Human Gene 1.0ST arrays, respectively. Both miRNA and gene expression profiles were integrated by correlation analysis to identify dysregulated miRNAs with their corresponding predicted target mRNA. Microarray data were validated with qRT-PCR. Regulation of IL8 and CDH11 expression by hsa-miR-200c-3p was determined by luciferase reporter assays. When comparing active UC patients vs. controls, 51 miRNAs and 1543 gene probe sets gave significantly different signals. In contrast, in inactive UC vs. controls, no significant miRNA expression differences were found while 155 gene probe sets had significantly different signals. We then identified potential target genes of the significantly dysregulated miRNAs and genes in active UC vs. controls and found a highly significant inverse correlation between hsa-miR-200c-3p and IL8, an inflammatory marker, and between hsa-miR-200c-3p and CDH11, a gene related to intestinal epithelial barrier function. We could demonstrate that hsa-miR-200c-3p directly regulates IL8 and CDH11 expression. Differential expression of immune- and barrier-related genes in inflamed UC mucosa may be influenced by altered expression of miRNAs. Integrated analysis of miRNA and mRNA expression profiles revealed hsa-miR-200c-3p for use of miRNA mimics as therapeutics.