Early life stress alters transcriptomic patterning across reward circuitry in male and female mice

Nat Commun. 2019 Nov 8;10(1):5098. doi: 10.1038/s41467-019-13085-6.

Abstract

Abuse, neglect, and other forms of early life stress (ELS) significantly increase risk for psychiatric disorders including depression. In this study, we show that ELS in a postnatal sensitive period increases sensitivity to adult stress in female mice, consistent with our earlier findings in male mice. We used RNA-sequencing in the ventral tegmental area, nucleus accumbens, and prefrontal cortex of male and female mice to show that adult stress is distinctly represented in the brain's transcriptome depending on ELS history. We identify: 1) biological pathways disrupted after ELS and associated with increased behavioral stress sensitivity, 2) putative transcriptional regulators of the effect of ELS on adult stress response, and 3) subsets of primed genes specifically associated with latent behavioral changes. We also provide transcriptomic evidence that ELS increases sensitivity to future stress through enhancement of known programs of cortical plasticity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Depression / genetics
  • Female
  • Gene Expression Profiling
  • Housing, Animal
  • Male
  • Maternal Deprivation*
  • Mice
  • Nucleus Accumbens / metabolism*
  • Prefrontal Cortex / metabolism*
  • Reward*
  • Sequence Analysis, RNA
  • Stress, Psychological / genetics*
  • Transcriptome*
  • Ventral Tegmental Area / metabolism*