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Prospects of Directly Reprogrammed Adult Human Neurons for Neurodegenerative Disease Modeling and Drug Discovery: iN vs. iPSCs Models

A reliable disease model is critical to the study of specific disease mechanisms as well as for the discovery and development of new drugs. Despite providing crucial insights into the mechanisms of neurodegenerative diseases, translation of this information to develop therapeutics in clinical trials...

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Autores principales: Zhang, Ying, Xie, Xinyang, Hu, Jiangnan, Afreen, Kazi Sabrina, Zhang, Chun-Li, Zhuge, Qichuan, Yang, Jianjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710799/
https://www.ncbi.nlm.nih.gov/pubmed/33328842
http://dx.doi.org/10.3389/fnins.2020.546484
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author Zhang, Ying
Xie, Xinyang
Hu, Jiangnan
Afreen, Kazi Sabrina
Zhang, Chun-Li
Zhuge, Qichuan
Yang, Jianjing
author_facet Zhang, Ying
Xie, Xinyang
Hu, Jiangnan
Afreen, Kazi Sabrina
Zhang, Chun-Li
Zhuge, Qichuan
Yang, Jianjing
author_sort Zhang, Ying
collection PubMed
description A reliable disease model is critical to the study of specific disease mechanisms as well as for the discovery and development of new drugs. Despite providing crucial insights into the mechanisms of neurodegenerative diseases, translation of this information to develop therapeutics in clinical trials have been unsuccessful. Reprogramming technology to convert adult somatic cells to induced Pluripotent Stem Cells (iPSCs) or directly reprogramming adult somatic cells to induced Neurons (iN), has allowed for the creation of better models to understand the molecular mechanisms and design of new drugs. In recent times, iPSC technology has been commonly used for modeling neurodegenerative diseases and drug discovery. However, several technological challenges have limited the application of iN. As evidence suggests, iN for the modeling of neurodegenerative disorders is advantageous compared to those derived from iPSCs. In this review, we will compare iPSCs and iN models for neurodegenerative diseases and their potential applications in the future.
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spelling pubmed-77107992020-12-15 Prospects of Directly Reprogrammed Adult Human Neurons for Neurodegenerative Disease Modeling and Drug Discovery: iN vs. iPSCs Models Zhang, Ying Xie, Xinyang Hu, Jiangnan Afreen, Kazi Sabrina Zhang, Chun-Li Zhuge, Qichuan Yang, Jianjing Front Neurosci Neuroscience A reliable disease model is critical to the study of specific disease mechanisms as well as for the discovery and development of new drugs. Despite providing crucial insights into the mechanisms of neurodegenerative diseases, translation of this information to develop therapeutics in clinical trials have been unsuccessful. Reprogramming technology to convert adult somatic cells to induced Pluripotent Stem Cells (iPSCs) or directly reprogramming adult somatic cells to induced Neurons (iN), has allowed for the creation of better models to understand the molecular mechanisms and design of new drugs. In recent times, iPSC technology has been commonly used for modeling neurodegenerative diseases and drug discovery. However, several technological challenges have limited the application of iN. As evidence suggests, iN for the modeling of neurodegenerative disorders is advantageous compared to those derived from iPSCs. In this review, we will compare iPSCs and iN models for neurodegenerative diseases and their potential applications in the future. Frontiers Media S.A. 2020-11-19 /pmc/articles/PMC7710799/ /pubmed/33328842 http://dx.doi.org/10.3389/fnins.2020.546484 Text en Copyright © 2020 Zhang, Xie, Hu, Afreen, Zhang, Zhuge and Yang. 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) and the copyright owner(s) 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
Zhang, Ying
Xie, Xinyang
Hu, Jiangnan
Afreen, Kazi Sabrina
Zhang, Chun-Li
Zhuge, Qichuan
Yang, Jianjing
Prospects of Directly Reprogrammed Adult Human Neurons for Neurodegenerative Disease Modeling and Drug Discovery: iN vs. iPSCs Models
title Prospects of Directly Reprogrammed Adult Human Neurons for Neurodegenerative Disease Modeling and Drug Discovery: iN vs. iPSCs Models
title_full Prospects of Directly Reprogrammed Adult Human Neurons for Neurodegenerative Disease Modeling and Drug Discovery: iN vs. iPSCs Models
title_fullStr Prospects of Directly Reprogrammed Adult Human Neurons for Neurodegenerative Disease Modeling and Drug Discovery: iN vs. iPSCs Models
title_full_unstemmed Prospects of Directly Reprogrammed Adult Human Neurons for Neurodegenerative Disease Modeling and Drug Discovery: iN vs. iPSCs Models
title_short Prospects of Directly Reprogrammed Adult Human Neurons for Neurodegenerative Disease Modeling and Drug Discovery: iN vs. iPSCs Models
title_sort prospects of directly reprogrammed adult human neurons for neurodegenerative disease modeling and drug discovery: in vs. ipscs models
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710799/
https://www.ncbi.nlm.nih.gov/pubmed/33328842
http://dx.doi.org/10.3389/fnins.2020.546484
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