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Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence

Since 2006, reprogrammed cells have increasingly been used as a biomedical research technique in addition to neuro‐psychiatric methods. These rapidly evolving techniques allow for the generation of neuronal sub‐populations, and have sparked interest not only in monogenetic neuro‐psychiatric diseases...

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Autores principales: Sauerzopf, Ulrich, Sacco, Roberto, Novarino, Gaia, Niello, Marco, Weidenauer, Ana, Praschak‐Rieder, Nicole, Sitte, Harald, Willeit, Matthäus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811827/
https://www.ncbi.nlm.nih.gov/pubmed/27690184
http://dx.doi.org/10.1111/ejn.13418
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author Sauerzopf, Ulrich
Sacco, Roberto
Novarino, Gaia
Niello, Marco
Weidenauer, Ana
Praschak‐Rieder, Nicole
Sitte, Harald
Willeit, Matthäus
author_facet Sauerzopf, Ulrich
Sacco, Roberto
Novarino, Gaia
Niello, Marco
Weidenauer, Ana
Praschak‐Rieder, Nicole
Sitte, Harald
Willeit, Matthäus
author_sort Sauerzopf, Ulrich
collection PubMed
description Since 2006, reprogrammed cells have increasingly been used as a biomedical research technique in addition to neuro‐psychiatric methods. These rapidly evolving techniques allow for the generation of neuronal sub‐populations, and have sparked interest not only in monogenetic neuro‐psychiatric diseases, but also in poly‐genetic and poly‐aetiological disorders such as schizophrenia (SCZ) and bipolar disorder (BPD). This review provides a summary of 19 publications on reprogrammed adult somatic cells derived from patients with SCZ, and five publications using this technique in patients with BPD. As both disorders are complex and heterogeneous, there is a plurality of hypotheses to be tested in vitro. In SCZ, data on alterations of dopaminergic transmission in vitro are sparse, despite the great explanatory power of the so‐called DA hypothesis of SCZ. Some findings correspond to perturbations of cell energy metabolism, and observations in reprogrammed cells suggest neuro‐developmental alterations. Some studies also report on the efficacy of medicinal compounds to revert alterations observed in cellular models. However, due to the paucity of replication studies, no comprehensive conclusions can be drawn from studies using reprogrammed cells at the present time. In the future, findings from cell culture methods need to be integrated with clinical, epidemiological, pharmacological and imaging data in order to generate a more comprehensive picture of SCZ and BPD.
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spelling pubmed-58118272018-02-16 Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence Sauerzopf, Ulrich Sacco, Roberto Novarino, Gaia Niello, Marco Weidenauer, Ana Praschak‐Rieder, Nicole Sitte, Harald Willeit, Matthäus Eur J Neurosci Reviews Since 2006, reprogrammed cells have increasingly been used as a biomedical research technique in addition to neuro‐psychiatric methods. These rapidly evolving techniques allow for the generation of neuronal sub‐populations, and have sparked interest not only in monogenetic neuro‐psychiatric diseases, but also in poly‐genetic and poly‐aetiological disorders such as schizophrenia (SCZ) and bipolar disorder (BPD). This review provides a summary of 19 publications on reprogrammed adult somatic cells derived from patients with SCZ, and five publications using this technique in patients with BPD. As both disorders are complex and heterogeneous, there is a plurality of hypotheses to be tested in vitro. In SCZ, data on alterations of dopaminergic transmission in vitro are sparse, despite the great explanatory power of the so‐called DA hypothesis of SCZ. Some findings correspond to perturbations of cell energy metabolism, and observations in reprogrammed cells suggest neuro‐developmental alterations. Some studies also report on the efficacy of medicinal compounds to revert alterations observed in cellular models. However, due to the paucity of replication studies, no comprehensive conclusions can be drawn from studies using reprogrammed cells at the present time. In the future, findings from cell culture methods need to be integrated with clinical, epidemiological, pharmacological and imaging data in order to generate a more comprehensive picture of SCZ and BPD. John Wiley and Sons Inc. 2016-10-19 2017-01 /pmc/articles/PMC5811827/ /pubmed/27690184 http://dx.doi.org/10.1111/ejn.13418 Text en © 2016 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Sauerzopf, Ulrich
Sacco, Roberto
Novarino, Gaia
Niello, Marco
Weidenauer, Ana
Praschak‐Rieder, Nicole
Sitte, Harald
Willeit, Matthäus
Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence
title Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence
title_full Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence
title_fullStr Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence
title_full_unstemmed Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence
title_short Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence
title_sort are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? a review of the current evidence
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811827/
https://www.ncbi.nlm.nih.gov/pubmed/27690184
http://dx.doi.org/10.1111/ejn.13418
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