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HDAC1 links early life stress to schizophrenia-like phenotypes
Schizophrenia is a devastating disease that arises on the background of genetic predisposition and environmental risk factors, such as early life stress (ELS). In this study, we show that ELS-induced schizophrenia-like phenotypes in mice correlate with a widespread increase of histone-deacetylase 1...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2017-06, Vol.114 (23), p.E4686-E4694 |
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container_title | Proceedings of the National Academy of Sciences - PNAS |
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creator | Bahari-Javan, Sanaz Varbanov, Hristo Halder, Rashi Benito, Eva Kaurani, Lalit Burkhardt, Susanne Anderson-Schmidt, Heike Anghelescu, Ion Budde, Monika Stilling, Roman M. Costa, Joan Medina, Juan Dietrich, Detlef E. Figge, Christian Folkerts, Here Gade, Katrin Heilbronner, Urs Koller, Manfred Konrad, Carsten Nussbeck, Sara Y. Scherk, Harald Spitzer, Carsten Stierl, Sebastian Stöckel, Judith Thiel, Andreas von Hagen, Martin Zimmermann, Jörg Zitzelsberger, Antje Schulz, Sybille Schmitt, Andrea Delalle, Ivana Falkai, Peter Schulze, Thomas G. Dityatev, Alexander Sananbenesi, Farahnaz Fischer, André |
description | Schizophrenia is a devastating disease that arises on the background of genetic predisposition and environmental risk factors, such as early life stress (ELS). In this study, we show that ELS-induced schizophrenia-like phenotypes in mice correlate with a widespread increase of histone-deacetylase 1 (Hdac1) expression that is linked to altered DNA methylation. Hdac1 overexpression in neurons of the medial prefrontal cortex, but not in the dorsal or ventral hippocampus, mimics schizophrenia-like phenotypes induced by ELS. Systemic administration of an HDAC inhibitor rescues the detrimental effects of ELS when applied after the manifestation of disease phenotypes. In addition to the hippocampus and prefrontal cortex, mice subjected to ELS exhibit increased Hdac1 expression in blood. Moreover, Hdac1 levels are increased in blood samples from patients with schizophrenia who had encountered ELS, compared with patients without ELS experience. Our data suggest that HDAC1 inhibition should be considered as a therapeutic approach to treat schizophrenia. |
doi_str_mv | 10.1073/pnas.1613842114 |
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In this study, we show that ELS-induced schizophrenia-like phenotypes in mice correlate with a widespread increase of histone-deacetylase 1 (Hdac1) expression that is linked to altered DNA methylation. Hdac1 overexpression in neurons of the medial prefrontal cortex, but not in the dorsal or ventral hippocampus, mimics schizophrenia-like phenotypes induced by ELS. Systemic administration of an HDAC inhibitor rescues the detrimental effects of ELS when applied after the manifestation of disease phenotypes. In addition to the hippocampus and prefrontal cortex, mice subjected to ELS exhibit increased Hdac1 expression in blood. Moreover, Hdac1 levels are increased in blood samples from patients with schizophrenia who had encountered ELS, compared with patients without ELS experience. Our data suggest that HDAC1 inhibition should be considered as a therapeutic approach to treat schizophrenia.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1613842114</identifier><identifier>PMID: 28533418</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Biological Sciences ; Blood ; Deoxyribonucleic acid ; DNA ; DNA methylation ; Environmental risk ; Gene expression ; Hippocampus ; Histone deacetylase ; Mental disorders ; Mice ; Neuropsychology ; Patients ; PNAS Plus ; Prefrontal cortex ; Risk analysis ; Risk factors ; Rodents ; Schizophrenia ; Stress</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2017-06, Vol.114 (23), p.E4686-E4694</ispartof><rights>Volumes 1–89 and 106–114, copyright as a collective work only; author(s) retains copyright to individual articles</rights><rights>Copyright National Academy of Sciences Jun 6, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-8eb1c6af57b1dc696315eda240e6f9e6fa89ea75a9f1e5679979d39c36dcc3f23</citedby><cites>FETCH-LOGICAL-c439t-8eb1c6af57b1dc696315eda240e6f9e6fa89ea75a9f1e5679979d39c36dcc3f23</cites><orcidid>0000-0002-1159-6538</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/26484175$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/26484175$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28533418$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bahari-Javan, Sanaz</creatorcontrib><creatorcontrib>Varbanov, Hristo</creatorcontrib><creatorcontrib>Halder, Rashi</creatorcontrib><creatorcontrib>Benito, Eva</creatorcontrib><creatorcontrib>Kaurani, Lalit</creatorcontrib><creatorcontrib>Burkhardt, Susanne</creatorcontrib><creatorcontrib>Anderson-Schmidt, Heike</creatorcontrib><creatorcontrib>Anghelescu, Ion</creatorcontrib><creatorcontrib>Budde, Monika</creatorcontrib><creatorcontrib>Stilling, Roman M.</creatorcontrib><creatorcontrib>Costa, Joan</creatorcontrib><creatorcontrib>Medina, Juan</creatorcontrib><creatorcontrib>Dietrich, Detlef E.</creatorcontrib><creatorcontrib>Figge, Christian</creatorcontrib><creatorcontrib>Folkerts, Here</creatorcontrib><creatorcontrib>Gade, Katrin</creatorcontrib><creatorcontrib>Heilbronner, Urs</creatorcontrib><creatorcontrib>Koller, Manfred</creatorcontrib><creatorcontrib>Konrad, Carsten</creatorcontrib><creatorcontrib>Nussbeck, Sara Y.</creatorcontrib><creatorcontrib>Scherk, Harald</creatorcontrib><creatorcontrib>Spitzer, Carsten</creatorcontrib><creatorcontrib>Stierl, Sebastian</creatorcontrib><creatorcontrib>Stöckel, Judith</creatorcontrib><creatorcontrib>Thiel, Andreas</creatorcontrib><creatorcontrib>von Hagen, Martin</creatorcontrib><creatorcontrib>Zimmermann, Jörg</creatorcontrib><creatorcontrib>Zitzelsberger, Antje</creatorcontrib><creatorcontrib>Schulz, Sybille</creatorcontrib><creatorcontrib>Schmitt, Andrea</creatorcontrib><creatorcontrib>Delalle, Ivana</creatorcontrib><creatorcontrib>Falkai, Peter</creatorcontrib><creatorcontrib>Schulze, Thomas G.</creatorcontrib><creatorcontrib>Dityatev, Alexander</creatorcontrib><creatorcontrib>Sananbenesi, Farahnaz</creatorcontrib><creatorcontrib>Fischer, André</creatorcontrib><title>HDAC1 links early life stress to schizophrenia-like phenotypes</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Schizophrenia is a devastating disease that arises on the background of genetic predisposition and environmental risk factors, such as early life stress (ELS). In this study, we show that ELS-induced schizophrenia-like phenotypes in mice correlate with a widespread increase of histone-deacetylase 1 (Hdac1) expression that is linked to altered DNA methylation. Hdac1 overexpression in neurons of the medial prefrontal cortex, but not in the dorsal or ventral hippocampus, mimics schizophrenia-like phenotypes induced by ELS. Systemic administration of an HDAC inhibitor rescues the detrimental effects of ELS when applied after the manifestation of disease phenotypes. In addition to the hippocampus and prefrontal cortex, mice subjected to ELS exhibit increased Hdac1 expression in blood. Moreover, Hdac1 levels are increased in blood samples from patients with schizophrenia who had encountered ELS, compared with patients without ELS experience. Our data suggest that HDAC1 inhibition should be considered as a therapeutic approach to treat schizophrenia.</description><subject>Biological Sciences</subject><subject>Blood</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA methylation</subject><subject>Environmental risk</subject><subject>Gene expression</subject><subject>Hippocampus</subject><subject>Histone deacetylase</subject><subject>Mental disorders</subject><subject>Mice</subject><subject>Neuropsychology</subject><subject>Patients</subject><subject>PNAS Plus</subject><subject>Prefrontal cortex</subject><subject>Risk analysis</subject><subject>Risk 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subjects | Biological Sciences Blood Deoxyribonucleic acid DNA DNA methylation Environmental risk Gene expression Hippocampus Histone deacetylase Mental disorders Mice Neuropsychology Patients PNAS Plus Prefrontal cortex Risk analysis Risk factors Rodents Schizophrenia Stress |
title | HDAC1 links early life stress to schizophrenia-like phenotypes |
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