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Direct Neuronal Reprogramming: Bridging the Gap Between Basic Science and Clinical Application

Direct neuronal reprogramming is an innovative new technology that involves the conversion of somatic cells to induced neurons (iNs) without passing through a pluripotent state. The capacity to make new neurons in the brain, which previously was not achievable, has created great excitement in the fi...

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Autores principales: Vasan, Lakshmy, Park, Eunjee, David, Luke Ajay, Fleming, Taylor, Schuurmans, Carol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287587/
https://www.ncbi.nlm.nih.gov/pubmed/34291049
http://dx.doi.org/10.3389/fcell.2021.681087
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author Vasan, Lakshmy
Park, Eunjee
David, Luke Ajay
Fleming, Taylor
Schuurmans, Carol
author_facet Vasan, Lakshmy
Park, Eunjee
David, Luke Ajay
Fleming, Taylor
Schuurmans, Carol
author_sort Vasan, Lakshmy
collection PubMed
description Direct neuronal reprogramming is an innovative new technology that involves the conversion of somatic cells to induced neurons (iNs) without passing through a pluripotent state. The capacity to make new neurons in the brain, which previously was not achievable, has created great excitement in the field as it has opened the door for the potential treatment of incurable neurodegenerative diseases and brain injuries such as stroke. These neurological disorders are associated with frank neuronal loss, and as new neurons are not made in most of the adult brain, treatment options are limited. Developmental biologists have paved the way for the field of direct neuronal reprogramming by identifying both intrinsic cues, primarily transcription factors (TFs) and miRNAs, and extrinsic cues, including growth factors and other signaling molecules, that induce neurogenesis and specify neuronal subtype identities in the embryonic brain. The striking observation that postmitotic, terminally differentiated somatic cells can be converted to iNs by mis-expression of TFs or miRNAs involved in neural lineage development, and/or by exposure to growth factors or small molecule cocktails that recapitulate the signaling environment of the developing brain, has opened the door to the rapid expansion of new neuronal reprogramming methodologies. Furthermore, the more recent applications of neuronal lineage conversion strategies that target resident glial cells in situ has expanded the clinical potential of direct neuronal reprogramming techniques. Herein, we present an overview of the history, accomplishments, and therapeutic potential of direct neuronal reprogramming as revealed over the last two decades.
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spelling pubmed-82875872021-07-20 Direct Neuronal Reprogramming: Bridging the Gap Between Basic Science and Clinical Application Vasan, Lakshmy Park, Eunjee David, Luke Ajay Fleming, Taylor Schuurmans, Carol Front Cell Dev Biol Cell and Developmental Biology Direct neuronal reprogramming is an innovative new technology that involves the conversion of somatic cells to induced neurons (iNs) without passing through a pluripotent state. The capacity to make new neurons in the brain, which previously was not achievable, has created great excitement in the field as it has opened the door for the potential treatment of incurable neurodegenerative diseases and brain injuries such as stroke. These neurological disorders are associated with frank neuronal loss, and as new neurons are not made in most of the adult brain, treatment options are limited. Developmental biologists have paved the way for the field of direct neuronal reprogramming by identifying both intrinsic cues, primarily transcription factors (TFs) and miRNAs, and extrinsic cues, including growth factors and other signaling molecules, that induce neurogenesis and specify neuronal subtype identities in the embryonic brain. The striking observation that postmitotic, terminally differentiated somatic cells can be converted to iNs by mis-expression of TFs or miRNAs involved in neural lineage development, and/or by exposure to growth factors or small molecule cocktails that recapitulate the signaling environment of the developing brain, has opened the door to the rapid expansion of new neuronal reprogramming methodologies. Furthermore, the more recent applications of neuronal lineage conversion strategies that target resident glial cells in situ has expanded the clinical potential of direct neuronal reprogramming techniques. Herein, we present an overview of the history, accomplishments, and therapeutic potential of direct neuronal reprogramming as revealed over the last two decades. Frontiers Media S.A. 2021-07-05 /pmc/articles/PMC8287587/ /pubmed/34291049 http://dx.doi.org/10.3389/fcell.2021.681087 Text en Copyright © 2021 Vasan, Park, David, Fleming and Schuurmans. https://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 Cell and Developmental Biology
Vasan, Lakshmy
Park, Eunjee
David, Luke Ajay
Fleming, Taylor
Schuurmans, Carol
Direct Neuronal Reprogramming: Bridging the Gap Between Basic Science and Clinical Application
title Direct Neuronal Reprogramming: Bridging the Gap Between Basic Science and Clinical Application
title_full Direct Neuronal Reprogramming: Bridging the Gap Between Basic Science and Clinical Application
title_fullStr Direct Neuronal Reprogramming: Bridging the Gap Between Basic Science and Clinical Application
title_full_unstemmed Direct Neuronal Reprogramming: Bridging the Gap Between Basic Science and Clinical Application
title_short Direct Neuronal Reprogramming: Bridging the Gap Between Basic Science and Clinical Application
title_sort direct neuronal reprogramming: bridging the gap between basic science and clinical application
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287587/
https://www.ncbi.nlm.nih.gov/pubmed/34291049
http://dx.doi.org/10.3389/fcell.2021.681087
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