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Effects of Early Life Stress on Epigenetic Changes of the Glucocorticoid Receptor 1(7) Promoter during Adulthood

Growing evidence suggests that early life stress (ELS) has long-lasting effects on glucocorticoid receptor (GR) expression and behavior via epigenetic changes of the GR exon 1(7) promoter. However, it remains unclear whether ELS regulates histone modifications of the GR exon 1(7) promoter across the...

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Detalles Bibliográficos
Autores principales: Seo, Mi Kyoung, Kim, Seon-gu, Seog, Dae-Hyun, Bahk, Won-Myong, Kim, Seong-Ho, Park, Sung Woo, Lee, Jung Goo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503815/
https://www.ncbi.nlm.nih.gov/pubmed/32878311
http://dx.doi.org/10.3390/ijms21176331
Descripción
Sumario:Growing evidence suggests that early life stress (ELS) has long-lasting effects on glucocorticoid receptor (GR) expression and behavior via epigenetic changes of the GR exon 1(7) promoter. However, it remains unclear whether ELS regulates histone modifications of the GR exon 1(7) promoter across the life span. We investigated the effects of maternal separation (MS) on histone acetylation and methylation of GR exon 1(7) promoter in the hippocampus, according to the age of adults. Depression-like behavior and epigenetic regulation of GR expression were examined at young and middle adulthood in mice subjected to MS from postnatal day 1 to 21. In the forced swimming test, young adult MS mice showed no effect on immobility time, but middle-aged MS mice significantly increased immobility time. Young adult and middle-aged MS mice showed decreased GR expression. Their two ages showed decreased histone acetylation with increased histone deacetylases (HDAC5) levels, decreased permissive methylation, and increased repressive methylation at the GR exon 1(7) promoter. The extent of changes in gene expression and histone modification in middle adulthood was greater than in young adulthood. These results indicate that MS in early life causes long-term negative effects on behavior via histone modification of the GR gene across the life span.