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Human-Induced Pluripotent Stem Cell Technology: Toward the Future of Personalized Psychiatry

The polygenic and multifactorial nature of many psychiatric disorders has hampered implementation of the personalized medicine approach in clinical practice. However, induced pluripotent stem cell (iPSC) technology has emerged as an innovative tool for patient-specific disease modeling to expand the...

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Autores principales: Alciati, Alessandra, Reggiani, Angelo, Caldirola, Daniela, Perna, Giampaolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410334/
https://www.ncbi.nlm.nih.gov/pubmed/36013289
http://dx.doi.org/10.3390/jpm12081340
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author Alciati, Alessandra
Reggiani, Angelo
Caldirola, Daniela
Perna, Giampaolo
author_facet Alciati, Alessandra
Reggiani, Angelo
Caldirola, Daniela
Perna, Giampaolo
author_sort Alciati, Alessandra
collection PubMed
description The polygenic and multifactorial nature of many psychiatric disorders has hampered implementation of the personalized medicine approach in clinical practice. However, induced pluripotent stem cell (iPSC) technology has emerged as an innovative tool for patient-specific disease modeling to expand the pathophysiology knowledge and treatment perspectives in the last decade. Current technologies enable adult human somatic cell reprogramming into iPSCs to generate neural cells and direct neural cell conversion to model organisms that exhibit phenotypes close to human diseases, thereby effectively representing relevant aspects of neuropsychiatric disorders. In this regard, iPSCs reflect patient pathophysiology and pharmacological responsiveness, particularly when cultured under conditions that emulate spatial tissue organization in brain organoids. Recently, the application of iPSCs has been frequently associated with gene editing that targets the disease-causing gene to deepen the illness pathophysiology and to conduct drug screening. Moreover, gene editing has provided a unique opportunity to repair the putative causative genetic lesions in patient-derived cells. Here, we review the use of iPSC technology to model and potentially treat neuropsychiatric disorders by illustrating the key studies on a series of mental disorders, including schizophrenia, major depressive disorder, bipolar disorder, and autism spectrum disorder. Future perspectives will involve the development of organ-on-a-chip platforms that control the microenvironmental conditions so as to reflect individual pathophysiological by adjusting physiochemical parameters according to personal health data. This strategy could open new ways by which to build a disease model that considers individual variability and tailors personalized treatments.
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spelling pubmed-94103342022-08-26 Human-Induced Pluripotent Stem Cell Technology: Toward the Future of Personalized Psychiatry Alciati, Alessandra Reggiani, Angelo Caldirola, Daniela Perna, Giampaolo J Pers Med Review The polygenic and multifactorial nature of many psychiatric disorders has hampered implementation of the personalized medicine approach in clinical practice. However, induced pluripotent stem cell (iPSC) technology has emerged as an innovative tool for patient-specific disease modeling to expand the pathophysiology knowledge and treatment perspectives in the last decade. Current technologies enable adult human somatic cell reprogramming into iPSCs to generate neural cells and direct neural cell conversion to model organisms that exhibit phenotypes close to human diseases, thereby effectively representing relevant aspects of neuropsychiatric disorders. In this regard, iPSCs reflect patient pathophysiology and pharmacological responsiveness, particularly when cultured under conditions that emulate spatial tissue organization in brain organoids. Recently, the application of iPSCs has been frequently associated with gene editing that targets the disease-causing gene to deepen the illness pathophysiology and to conduct drug screening. Moreover, gene editing has provided a unique opportunity to repair the putative causative genetic lesions in patient-derived cells. Here, we review the use of iPSC technology to model and potentially treat neuropsychiatric disorders by illustrating the key studies on a series of mental disorders, including schizophrenia, major depressive disorder, bipolar disorder, and autism spectrum disorder. Future perspectives will involve the development of organ-on-a-chip platforms that control the microenvironmental conditions so as to reflect individual pathophysiological by adjusting physiochemical parameters according to personal health data. This strategy could open new ways by which to build a disease model that considers individual variability and tailors personalized treatments. MDPI 2022-08-20 /pmc/articles/PMC9410334/ /pubmed/36013289 http://dx.doi.org/10.3390/jpm12081340 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Alciati, Alessandra
Reggiani, Angelo
Caldirola, Daniela
Perna, Giampaolo
Human-Induced Pluripotent Stem Cell Technology: Toward the Future of Personalized Psychiatry
title Human-Induced Pluripotent Stem Cell Technology: Toward the Future of Personalized Psychiatry
title_full Human-Induced Pluripotent Stem Cell Technology: Toward the Future of Personalized Psychiatry
title_fullStr Human-Induced Pluripotent Stem Cell Technology: Toward the Future of Personalized Psychiatry
title_full_unstemmed Human-Induced Pluripotent Stem Cell Technology: Toward the Future of Personalized Psychiatry
title_short Human-Induced Pluripotent Stem Cell Technology: Toward the Future of Personalized Psychiatry
title_sort human-induced pluripotent stem cell technology: toward the future of personalized psychiatry
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410334/
https://www.ncbi.nlm.nih.gov/pubmed/36013289
http://dx.doi.org/10.3390/jpm12081340
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