MicroRNA-326 acts as a molecular switch in the regulation of midbrain urocortin 1 expression

• Published in: Journal of psychiatry & neuroscience 2016-09, Vol.41 (5), p.342-353
• Main Authors: Aschrafi, Armaz, PhD, Verheijen, Jan M., MSc, Gordebeke, Peter M., MSc, Menting, Kelly, MSc, Geenen, Bram, MSc, Kozicz, Tamas, MD, PhD, Olde Loohuis, Nikkie F., MSc, Jager, Amanda, MSc, Kos, Aron, MSc, Glennon, Jeffrey C., PhD, Palkovits, Miklos, MD, PhD, DSc, Martens, Gerard J.M., PhD, Kaplan, Barry B., PhD, Gaszner, Balázs, MD, PhD
• Format: Article
• Language: English
• Subjects: Adult; Anatomy & physiology; Animals; Binding Sites; Brain research; Cells, Cultured; Chronic Disease; Computer Simulation; Depressive Disorder - metabolism; Disease Models, Animal; Down-Regulation; Experiments; Gene expression; Genetic aspects; Health aspects; Humans; Male; Medical Education; Mesencephalon - metabolism; MicroRNA; MicroRNAs; MicroRNAs - metabolism; Middle Aged; Neurons - metabolism; Neuropeptides; Neurosciences; Psychiatry; Rats, Wistar; Research Paper; RNA, Messenger - metabolism; Stress response; Stress, Psychological; Suicidal behavior; Suicide; Suicides & suicide attempts; Urocortins - metabolism
• ISSN: 1180-4882; 1488-2434
• DOI: 10.1503/jpn.150154

Background Altered levels of urocortin 1 (Ucn1) in the centrally projecting Edinger–Westphal nucleus (EWcp) of depressed suicide attempters or completers mediate the brain’s response to stress, while the mechanism regulating Ucn1 expression is unknown. We tested the hypothesis that microRNAs (miRNAs), which are vital fine-tuners of gene expression during the brain’s response to stress, have the capacity to modulate Ucn1 expression. Methods Computational analysis revealed that the Ucn1 3′ untranslated region contained a conserved binding site for miR-326. We examined miR-326 and Ucn1 levels in the EWcp of depressed suicide completers. In addition, we evaluated miR-326 and Ucn1 levels in the serum and the EWcp of a chronic variable mild stress (CVMS) rat model of behavioural despair and after recovery from CVMS, respectively. Gain and loss of miR-326 function experiments examined the regulation of Ucn1 by this miRNA in cultured midbrain neurons. Results We found reduced miR-326 levels concomitant with elevated Ucn1 levels in the EWcp of depressed suicide completers as well as in the EWcp of CVMS rats. In CVMS rats fully recovered from stress, both serum and EWcp miR-326 levels rebounded to nonstressed levels. While downregulation of miR-326 levels in primary midbrain neurons enhanced Ucn1 expression levels, miR-326 overexpression selectively reduced the levels of this neuropeptide. Limitations This study lacked experiments showing that in vivo alteration of miR-326 levels alleviate depression-like behaviours. We show only correlative data for miR-325 and cocaine- and amphetamine-regulated transcript levels in the EWcp. Conclusion We identified miR-326 dysregulation in depressed suicide completers and characterized this miRNA as an upstream regulator of the Ucn1 neuropeptide expression in midbrain neurons.