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Direct Neuronal Reprogramming for Disease Modeling Studies Using Patient-Derived Neurons: What Have We Learned?

Direct neuronal reprogramming, by which a neuron is formed via direct conversion from a somatic cell without going through a pluripotent intermediate stage, allows for the possibility of generating patient-derived neurons. A unique feature of these so-called induced neurons (iNs) is the potential to...

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Autores principales: Drouin-Ouellet, Janelle, Pircs, Karolina, Barker, Roger A., Jakobsson, Johan, Parmar, Malin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625013/
https://www.ncbi.nlm.nih.gov/pubmed/29033781
http://dx.doi.org/10.3389/fnins.2017.00530
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author Drouin-Ouellet, Janelle
Pircs, Karolina
Barker, Roger A.
Jakobsson, Johan
Parmar, Malin
author_facet Drouin-Ouellet, Janelle
Pircs, Karolina
Barker, Roger A.
Jakobsson, Johan
Parmar, Malin
author_sort Drouin-Ouellet, Janelle
collection PubMed
description Direct neuronal reprogramming, by which a neuron is formed via direct conversion from a somatic cell without going through a pluripotent intermediate stage, allows for the possibility of generating patient-derived neurons. A unique feature of these so-called induced neurons (iNs) is the potential to maintain aging and epigenetic signatures of the donor, which is critical given that many diseases of the CNS are age related. Here, we review the published literature on the work that has been undertaken using iNs to model human brain disorders. Furthermore, as disease-modeling studies using this direct neuronal reprogramming approach are becoming more widely adopted, it is important to assess the criteria that are used to characterize the iNs, especially in relation to the extent to which they are mature adult neurons. In particular: i) what constitutes an iN cell, ii) which stages of conversion offer the earliest/optimal time to assess features that are specific to neurons and/or a disorder and iii) whether generating subtype-specific iNs is critical to the disease-related features that iNs express. Finally, we discuss the range of potential biomedical applications that can be explored using patient-specific models of neurological disorders with iNs, and the challenges that will need to be overcome in order to realize these applications.
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spelling pubmed-56250132017-10-13 Direct Neuronal Reprogramming for Disease Modeling Studies Using Patient-Derived Neurons: What Have We Learned? Drouin-Ouellet, Janelle Pircs, Karolina Barker, Roger A. Jakobsson, Johan Parmar, Malin Front Neurosci Neuroscience Direct neuronal reprogramming, by which a neuron is formed via direct conversion from a somatic cell without going through a pluripotent intermediate stage, allows for the possibility of generating patient-derived neurons. A unique feature of these so-called induced neurons (iNs) is the potential to maintain aging and epigenetic signatures of the donor, which is critical given that many diseases of the CNS are age related. Here, we review the published literature on the work that has been undertaken using iNs to model human brain disorders. Furthermore, as disease-modeling studies using this direct neuronal reprogramming approach are becoming more widely adopted, it is important to assess the criteria that are used to characterize the iNs, especially in relation to the extent to which they are mature adult neurons. In particular: i) what constitutes an iN cell, ii) which stages of conversion offer the earliest/optimal time to assess features that are specific to neurons and/or a disorder and iii) whether generating subtype-specific iNs is critical to the disease-related features that iNs express. Finally, we discuss the range of potential biomedical applications that can be explored using patient-specific models of neurological disorders with iNs, and the challenges that will need to be overcome in order to realize these applications. Frontiers Media S.A. 2017-09-28 /pmc/articles/PMC5625013/ /pubmed/29033781 http://dx.doi.org/10.3389/fnins.2017.00530 Text en Copyright © 2017 Drouin-Ouellet, Pircs, Barker, Jakobsson and Parmar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Drouin-Ouellet, Janelle
Pircs, Karolina
Barker, Roger A.
Jakobsson, Johan
Parmar, Malin
Direct Neuronal Reprogramming for Disease Modeling Studies Using Patient-Derived Neurons: What Have We Learned?
title Direct Neuronal Reprogramming for Disease Modeling Studies Using Patient-Derived Neurons: What Have We Learned?
title_full Direct Neuronal Reprogramming for Disease Modeling Studies Using Patient-Derived Neurons: What Have We Learned?
title_fullStr Direct Neuronal Reprogramming for Disease Modeling Studies Using Patient-Derived Neurons: What Have We Learned?
title_full_unstemmed Direct Neuronal Reprogramming for Disease Modeling Studies Using Patient-Derived Neurons: What Have We Learned?
title_short Direct Neuronal Reprogramming for Disease Modeling Studies Using Patient-Derived Neurons: What Have We Learned?
title_sort direct neuronal reprogramming for disease modeling studies using patient-derived neurons: what have we learned?
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625013/
https://www.ncbi.nlm.nih.gov/pubmed/29033781
http://dx.doi.org/10.3389/fnins.2017.00530
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