miR-218 in Adolescence Predicts and Mediates Vulnerability to Stress

被引:28
|
作者
Torres-Berrio, Angelica [1 ,4 ,5 ]
Morgunova, Alice [1 ,3 ]
Giroux, Michel [3 ]
Cuesta, Santiago [3 ]
Nestler, Eric J. [4 ,5 ]
Flores, Cecilia [2 ,3 ]
机构
[1] McGill Univ, Integrated Program Neurosci, Montreal, PQ, Canada
[2] McGill Univ, Dept Psychiat, Montreal, PQ, Canada
[3] McGill Univ, Douglas Mental Hlth Univ Inst, Montreal, PQ, Canada
[4] Icahn Sch Med Mt Sinai, Nash Family Dept Neurosci, New York, NY 10029 USA
[5] Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA
关键词
MAJOR DEPRESSIVE DISORDER; GENOME-WIDE ASSOCIATION; PREFRONTAL CORTEX; ENVIRONMENT INTERACTION; INTRANASAL DELIVERY; DIURNAL CORTISOL; UK BIOBANK; MICRORNA; ONSET; DCC;
D O I
10.1016/j.biopsych.2020.10.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
BACKGROUND: Adolescence is a period of increased vulnerability to psychiatric disorders, including depression. Discovering novel biomarkers to identify individuals who are at high risk is very much needed. Our previous work shows that the microRNA miR-218 mediates susceptibility to stress and depression in adulthood by targeting the netrin-1 guidance cue receptor gene Dcc in the medial prefrontal cortex (mPFC). METHODS: Here, we investigated whether miR-218 regulates Dcc expression in adolescence and could serve as an early predictor of lifetime stress vulnerability in male mice. RESULTS: miR-218 expression in the mPFC increases from early adolescence to adulthood and correlates negatively with Dcc levels. In blood, postnatal miR-218 expression parallels changes occurring in the mPFC. Notably, circulating miR-218 levels in adolescence associate with vulnerability to social defeat stress in adulthood, with high levels associated with social avoidance severity. Indeed, downregulation of miR-218 in the mPFC in adolescence promotes resilience to stress in adulthood. CONCLUSIONS: miR-218 expression in adolescence may serve both as a marker of risk and as a target for early interventions.
引用
收藏
页码:911 / 919
页数:9
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