Early life stress alters transcriptomic patterning across reward circuitry in male and female mice
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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.
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Early life stress may not cause immediate behavioral abnormalities but instead causes long-lasting transcriptional alterations that prime critical brain regions to be hyper-responsive to later stress and prone to develop a depression-like state.
“ELS may not cause immediate behavioral abnormalities but instead causes long-lasting transcriptional alterations that prime critical brain regions to be hyper-responsive to later stress and prone to develop a depression-like state.209,210”
From Epigenetic regulation in major depression and other stress-related disorders: molecular mechanisms, clinical relevance and therapeutic potential (2023) · cites this paper as [210]
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References 92 · Cited by 219
Research works printed but not linked: 1
- [85]Smyth, G. K. In Bioinformatics and Computational Biology Solutions Using R and Bioconductor 397–420 (Springer-Verlag, 2005).
- Authors
- Peña, C. J., Smith, M., Ramakrishnan, A., Cates, H. M., Bagot, R. C., Kronman, H. G., Patel, B., Chang, A. B., Purushothaman, I., Dudley, J., Morishita, H., Shen, L., & Nestler, E. J.
- Affiliations
- Princeton University (US)
- Icahn School of Medicine at Mount Sinai (US)
- McGill University (CA)
- Corresponding author
- Peña, Catherine Jensen
- Nestler, Eric J.
- ORCID
- Venue
- Nature Communications
- Published
- 2019-11-08
- Volume
- 10
- Issue
- 1
- Pages
- 5098-5098
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC6841985
- OpenAlex
- W2986023816
- Cited by
- 219
- References
- 92
- Citations by year
- 2026: 26 · 2025: 40 · 2024: 26 · 2023: 45 · 2022: 33 · 2021: 35 · 2020: 14
- FWCI
- 13.40
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (5K99MH115096, P50MH096890, R01MH51399)
- Hope for Depression Research Foundation
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Social Sciences › Psychology › Clinical Psychology › Child Abuse and Trauma
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- early life stress, reward systems, ventral tegmental area, nucleus accumbens, prefrontal cortex, sex differences, transcriptome, depression risk, cortical plasticity, transcription factors, gene expression
- MeSH terms
- Animals, Depression, Female, Housing, Animal, Male, Maternal Deprivation, Nucleus Accumbens, Reward, Stress, Psychological, Prefrontal Cortex, Sequence Analysis, RNA, Ventral Tegmental Area, Gene Expression Profiling, Mice, Transcriptome
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