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Early life stress alters transcriptomic patterning across reward circuitry in male and female mice
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 mi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6841985/ https://www.ncbi.nlm.nih.gov/pubmed/31704941 http://dx.doi.org/10.1038/s41467-019-13085-6 |
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author | Peña, Catherine Jensen Smith, Milo Ramakrishnan, Aarthi Cates, Hannah M. Bagot, Rosemary C. Kronman, Hope G. Patel, Bhakti Chang, Austin B. Purushothaman, Immanuel Dudley, Joel Morishita, Hirofumi Shen, Li Nestler, Eric J. |
author_facet | Peña, Catherine Jensen Smith, Milo Ramakrishnan, Aarthi Cates, Hannah M. Bagot, Rosemary C. Kronman, Hope G. Patel, Bhakti Chang, Austin B. Purushothaman, Immanuel Dudley, Joel Morishita, Hirofumi Shen, Li Nestler, Eric J. |
author_sort | Peña, Catherine Jensen |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6841985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68419852019-11-13 Early life stress alters transcriptomic patterning across reward circuitry in male and female mice Peña, Catherine Jensen Smith, Milo Ramakrishnan, Aarthi Cates, Hannah M. Bagot, Rosemary C. Kronman, Hope G. Patel, Bhakti Chang, Austin B. Purushothaman, Immanuel Dudley, Joel Morishita, Hirofumi Shen, Li Nestler, Eric J. Nat Commun Article 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. Nature Publishing Group UK 2019-11-08 /pmc/articles/PMC6841985/ /pubmed/31704941 http://dx.doi.org/10.1038/s41467-019-13085-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Peña, Catherine Jensen Smith, Milo Ramakrishnan, Aarthi Cates, Hannah M. Bagot, Rosemary C. Kronman, Hope G. Patel, Bhakti Chang, Austin B. Purushothaman, Immanuel Dudley, Joel Morishita, Hirofumi Shen, Li Nestler, Eric J. Early life stress alters transcriptomic patterning across reward circuitry in male and female mice |
title | Early life stress alters transcriptomic patterning across reward circuitry in male and female mice |
title_full | Early life stress alters transcriptomic patterning across reward circuitry in male and female mice |
title_fullStr | Early life stress alters transcriptomic patterning across reward circuitry in male and female mice |
title_full_unstemmed | Early life stress alters transcriptomic patterning across reward circuitry in male and female mice |
title_short | Early life stress alters transcriptomic patterning across reward circuitry in male and female mice |
title_sort | early life stress alters transcriptomic patterning across reward circuitry in male and female mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6841985/ https://www.ncbi.nlm.nih.gov/pubmed/31704941 http://dx.doi.org/10.1038/s41467-019-13085-6 |
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