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Gadd45b mediates depressive-like role through DNA demethylation

Animal studies using chronic social defeat stress (CSDS) in mice showed that brain-derived neurotrophic factor (BDNF) signaling in the mesolimbic dopamine (DA) circuit is important for the development of social aversion. However, the downstream molecular targets after BDNF release from ventral tegme...

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Autores principales: Labonté, Benoit, Jeong, Yun Ha, Parise, Eric, Issler, Orna, Fatma, Mena, Engmann, Olivia, Cho, Kyung-Ah, Neve, Rachael, Nestler, Eric J., Koo, Ja Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420662/
https://www.ncbi.nlm.nih.gov/pubmed/30874581
http://dx.doi.org/10.1038/s41598-019-40844-8
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author Labonté, Benoit
Jeong, Yun Ha
Parise, Eric
Issler, Orna
Fatma, Mena
Engmann, Olivia
Cho, Kyung-Ah
Neve, Rachael
Nestler, Eric J.
Koo, Ja Wook
author_facet Labonté, Benoit
Jeong, Yun Ha
Parise, Eric
Issler, Orna
Fatma, Mena
Engmann, Olivia
Cho, Kyung-Ah
Neve, Rachael
Nestler, Eric J.
Koo, Ja Wook
author_sort Labonté, Benoit
collection PubMed
description Animal studies using chronic social defeat stress (CSDS) in mice showed that brain-derived neurotrophic factor (BDNF) signaling in the mesolimbic dopamine (DA) circuit is important for the development of social aversion. However, the downstream molecular targets after BDNF release from ventral tegmental area (VTA) DA terminals are unknown. Here, we show that depressive-like behaviors induced by CSDS are mediated in part by Gadd45b downstream of BDNF signaling in the nucleus accumbens (NAc). We show that Gadd45b mRNA levels are increased in susceptible but not resilient mice. Intra-NAc infusion of BDNF or optical stimulation of VTA DA terminals in NAc enhanced Gadd45b expression levels in the NAc. Importantly, Gadd45b downregulation reversed social avoidance in susceptible mice. Together, these data suggest that Gadd45b in NAc contributes to susceptibility to social stress. In addition, we investigated the function of Gadd45b in demethylating CpG islands of representative gene targets, which have been associated with a depressive phenotype in humans and animal models. We found that Gadd45b downregulation changes DNA methylation levels in a phenotype-, gene-, and locus-specific fashion. Together, these results highlight the contribution of Gadd45b and changes in DNA methylation in mediating the effects of social stress in the mesolimbic DA circuit.
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spelling pubmed-64206622019-03-19 Gadd45b mediates depressive-like role through DNA demethylation Labonté, Benoit Jeong, Yun Ha Parise, Eric Issler, Orna Fatma, Mena Engmann, Olivia Cho, Kyung-Ah Neve, Rachael Nestler, Eric J. Koo, Ja Wook Sci Rep Article Animal studies using chronic social defeat stress (CSDS) in mice showed that brain-derived neurotrophic factor (BDNF) signaling in the mesolimbic dopamine (DA) circuit is important for the development of social aversion. However, the downstream molecular targets after BDNF release from ventral tegmental area (VTA) DA terminals are unknown. Here, we show that depressive-like behaviors induced by CSDS are mediated in part by Gadd45b downstream of BDNF signaling in the nucleus accumbens (NAc). We show that Gadd45b mRNA levels are increased in susceptible but not resilient mice. Intra-NAc infusion of BDNF or optical stimulation of VTA DA terminals in NAc enhanced Gadd45b expression levels in the NAc. Importantly, Gadd45b downregulation reversed social avoidance in susceptible mice. Together, these data suggest that Gadd45b in NAc contributes to susceptibility to social stress. In addition, we investigated the function of Gadd45b in demethylating CpG islands of representative gene targets, which have been associated with a depressive phenotype in humans and animal models. We found that Gadd45b downregulation changes DNA methylation levels in a phenotype-, gene-, and locus-specific fashion. Together, these results highlight the contribution of Gadd45b and changes in DNA methylation in mediating the effects of social stress in the mesolimbic DA circuit. Nature Publishing Group UK 2019-03-15 /pmc/articles/PMC6420662/ /pubmed/30874581 http://dx.doi.org/10.1038/s41598-019-40844-8 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
Labonté, Benoit
Jeong, Yun Ha
Parise, Eric
Issler, Orna
Fatma, Mena
Engmann, Olivia
Cho, Kyung-Ah
Neve, Rachael
Nestler, Eric J.
Koo, Ja Wook
Gadd45b mediates depressive-like role through DNA demethylation
title Gadd45b mediates depressive-like role through DNA demethylation
title_full Gadd45b mediates depressive-like role through DNA demethylation
title_fullStr Gadd45b mediates depressive-like role through DNA demethylation
title_full_unstemmed Gadd45b mediates depressive-like role through DNA demethylation
title_short Gadd45b mediates depressive-like role through DNA demethylation
title_sort gadd45b mediates depressive-like role through dna demethylation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420662/
https://www.ncbi.nlm.nih.gov/pubmed/30874581
http://dx.doi.org/10.1038/s41598-019-40844-8
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