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THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorders

There is a strong association between cannabis use and schizophrenia but the underlying cellular links are poorly understood. Neurons derived from human-induced pluripotent stem cells (hiPSCs) offer a platform for investigating both baseline and dynamic changes in human neural cells. Here, we expose...

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Autores principales: Guennewig, Boris, Bitar, Maina, Obiorah, Ifeanyi, Hanks, James, O’Brien, Elizabeth A., Kaczorowski, Dominik C., Hurd, Yasmin L., Roussos, Panos, Brennand, Kristen J., Barry, Guy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915454/
https://www.ncbi.nlm.nih.gov/pubmed/29691375
http://dx.doi.org/10.1038/s41398-018-0137-3
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author Guennewig, Boris
Bitar, Maina
Obiorah, Ifeanyi
Hanks, James
O’Brien, Elizabeth A.
Kaczorowski, Dominik C.
Hurd, Yasmin L.
Roussos, Panos
Brennand, Kristen J.
Barry, Guy
author_facet Guennewig, Boris
Bitar, Maina
Obiorah, Ifeanyi
Hanks, James
O’Brien, Elizabeth A.
Kaczorowski, Dominik C.
Hurd, Yasmin L.
Roussos, Panos
Brennand, Kristen J.
Barry, Guy
author_sort Guennewig, Boris
collection PubMed
description There is a strong association between cannabis use and schizophrenia but the underlying cellular links are poorly understood. Neurons derived from human-induced pluripotent stem cells (hiPSCs) offer a platform for investigating both baseline and dynamic changes in human neural cells. Here, we exposed neurons derived from hiPSCs to Δ(9)-tetrahydrocannabinol (THC), and identified diagnosis-specific differences not detectable in vehicle-controls. RNA transcriptomic analyses revealed that THC administration, either by acute or chronic exposure, dampened the neuronal transcriptional response following potassium chloride (KCl)-induced neuronal depolarization. THC-treated neurons displayed significant synaptic, mitochondrial, and glutamate signaling alterations that may underlie their failure to activate appropriately; this blunted response resembles effects previously observed in schizophrenia hiPSC- derived neurons. Furthermore, we show a significant alteration in THC-related genes associated with autism and intellectual disability, suggesting shared molecular pathways perturbed in neuropsychiatric disorders that are exacerbated by THC.
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spelling pubmed-59154542018-04-25 THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorders Guennewig, Boris Bitar, Maina Obiorah, Ifeanyi Hanks, James O’Brien, Elizabeth A. Kaczorowski, Dominik C. Hurd, Yasmin L. Roussos, Panos Brennand, Kristen J. Barry, Guy Transl Psychiatry Article There is a strong association between cannabis use and schizophrenia but the underlying cellular links are poorly understood. Neurons derived from human-induced pluripotent stem cells (hiPSCs) offer a platform for investigating both baseline and dynamic changes in human neural cells. Here, we exposed neurons derived from hiPSCs to Δ(9)-tetrahydrocannabinol (THC), and identified diagnosis-specific differences not detectable in vehicle-controls. RNA transcriptomic analyses revealed that THC administration, either by acute or chronic exposure, dampened the neuronal transcriptional response following potassium chloride (KCl)-induced neuronal depolarization. THC-treated neurons displayed significant synaptic, mitochondrial, and glutamate signaling alterations that may underlie their failure to activate appropriately; this blunted response resembles effects previously observed in schizophrenia hiPSC- derived neurons. Furthermore, we show a significant alteration in THC-related genes associated with autism and intellectual disability, suggesting shared molecular pathways perturbed in neuropsychiatric disorders that are exacerbated by THC. Nature Publishing Group UK 2018-04-25 /pmc/articles/PMC5915454/ /pubmed/29691375 http://dx.doi.org/10.1038/s41398-018-0137-3 Text en © The Author(s) 2018 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
Guennewig, Boris
Bitar, Maina
Obiorah, Ifeanyi
Hanks, James
O’Brien, Elizabeth A.
Kaczorowski, Dominik C.
Hurd, Yasmin L.
Roussos, Panos
Brennand, Kristen J.
Barry, Guy
THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorders
title THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorders
title_full THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorders
title_fullStr THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorders
title_full_unstemmed THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorders
title_short THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorders
title_sort thc exposure of human ipsc neurons impacts genes associated with neuropsychiatric disorders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915454/
https://www.ncbi.nlm.nih.gov/pubmed/29691375
http://dx.doi.org/10.1038/s41398-018-0137-3
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