Chronic academic stress increases a group of microRNAs in peripheral blood

PLoS One. 2013 Oct 9;8(10):e75960. doi: 10.1371/journal.pone.0075960. eCollection 2013.

Abstract

MicroRNAs (miRNAs) play key roles in regulation of cellular processes in response to changes in environment. In this study, we examined alterations in miRNA profiles in peripheral blood from 25 male medical students two months and two days before the National Examination for Medical Practitioners. Blood obtained one month after the examination were used as baseline controls. Levels of seven miRNAs (miR-16, -20b, -26b, -29a, -126, -144 and -144*) were significantly elevated during the pre-examination period in association with significant down-regulation of their target mRNAs (WNT4, CCM2, MAK, and FGFR1 mRNAs) two days before the examination. State anxiety assessed two months before the examination was positively and negatively correlated with miR-16 and its target WNT4 mRNA levels, respectively. Fold changes in miR-16 levels from two days before to one month after the examination were inversely correlated with those in WNT4 mRNA levels over the same time points. We also confirmed the interaction between miR-16 and WNT4 3'UTR in HEK293T cells overexpressing FLAG-tagged WNT4 3'UTR and miR-16. Thus, a distinct group of miRNAs in periheral blood may participate in the integrated response to chronic academic stress in healthy young men.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Carrier Proteins / genetics
  • Humans
  • Male
  • MicroRNAs / genetics*
  • Protein-Serine-Threonine Kinases / genetics
  • Receptor, Fibroblast Growth Factor, Type 1 / genetics
  • Stress, Psychological / genetics*
  • Teaching*
  • Wnt4 Protein / genetics

Substances

  • CCM2 protein, human
  • Carrier Proteins
  • MIRN126 microRNA, human
  • MIRN144 microRNA, human
  • MIRN16 microRNA, human
  • MIRN20a microRNA, human
  • MIRN26A microRNA, human
  • MIRN29 microRNA, human
  • MicroRNAs
  • WNT4 protein, human
  • Wnt4 Protein
  • FGFR1 protein, human
  • Receptor, Fibroblast Growth Factor, Type 1
  • Protein-Serine-Threonine Kinases
  • MAK protein, human

Grant support

This study was supported in part by grants from from Grants-in-Aid for Scientific Research B (22390146) and Grant-in-Aid for Challenging Exploratory Research (22659142) from the Japan Society for the Promotion of Science (to KR). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.