Early life stress confers lifelong stress susceptibility in mice via ventral tegmental area OTX2

Science. 2017 Jun 16;356(6343):1185-1188. doi: 10.1126/science.aan4491.

Abstract

Early life stress increases risk for depression. Here we establish a "two-hit" stress model in mice wherein stress at a specific postnatal period increases susceptibility to adult social defeat stress and causes long-lasting transcriptional alterations that prime the ventral tegmental area (VTA)-a brain reward region-to be in a depression-like state. We identify a role for the developmental transcription factor orthodenticle homeobox 2 (Otx2) as an upstream mediator of these enduring effects. Transient juvenile-but not adult-knockdown of Otx2 in VTA mimics early life stress by increasing stress susceptibility, whereas its overexpression reverses the effects of early life stress. This work establishes a mechanism by which early life stress encodes lifelong susceptibility to stress via long-lasting transcriptional programming in VTA mediated by Otx2.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Age Factors
  • Animals
  • Depression / genetics*
  • Depression / physiopathology
  • Female
  • Gene Expression Regulation*
  • Gene Knockdown Techniques
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Otx Transcription Factors / genetics*
  • Protein Binding
  • Stress, Physiological / genetics*
  • Ventral Tegmental Area / physiopathology*

Substances

  • Otx Transcription Factors
  • Otx2 protein, mouse