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Long‐Distance Axonal Growth and Protracted Functional Maturation of Neurons Derived from Human Induced Pluripotent Stem Cells After Intracerebral Transplantation

The capacity for induced pluripotent stem (iPS) cells to be differentiated into a wide range of neural cell types makes them an attractive donor source for autologous neural transplantation therapies aimed at brain repair. Translation to the in vivo setting has been difficult, however, with mixed re...

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Autores principales: Niclis, Jonathan C., Turner, Christopher, Durnall, Jennifer, McDougal, Stuart, Kauhausen, Jessica A., Leaw, Bryan, Dottori, Mirella, Parish, Clare L., Thompson, Lachlan H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689777/
https://www.ncbi.nlm.nih.gov/pubmed/28198124
http://dx.doi.org/10.1002/sctm.16-0198
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author Niclis, Jonathan C.
Turner, Christopher
Durnall, Jennifer
McDougal, Stuart
Kauhausen, Jessica A.
Leaw, Bryan
Dottori, Mirella
Parish, Clare L.
Thompson, Lachlan H.
author_facet Niclis, Jonathan C.
Turner, Christopher
Durnall, Jennifer
McDougal, Stuart
Kauhausen, Jessica A.
Leaw, Bryan
Dottori, Mirella
Parish, Clare L.
Thompson, Lachlan H.
author_sort Niclis, Jonathan C.
collection PubMed
description The capacity for induced pluripotent stem (iPS) cells to be differentiated into a wide range of neural cell types makes them an attractive donor source for autologous neural transplantation therapies aimed at brain repair. Translation to the in vivo setting has been difficult, however, with mixed results in a wide variety of preclinical models of brain injury and limited information on the basic in vivo properties of neural grafts generated from human iPS cells. Here we have generated a human iPS cell line constitutively expressing green fluorescent protein as a basis to identify and characterize grafts resulting from transplantation of neural progenitors into the adult rat brain. The results show that the grafts contain a mix of neural cell types, at various stages of differentiation, including neurons that establish extensive patterns of axonal growth and progressively develop functional properties over the course of 1 year after implantation. These findings form an important basis for the design and interpretation of preclinical studies using human stem cells for functional circuit re‐construction in animal models of brain injury. Stem Cells Translational Medicine 2017;6:1547–1556
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spelling pubmed-56897772017-11-24 Long‐Distance Axonal Growth and Protracted Functional Maturation of Neurons Derived from Human Induced Pluripotent Stem Cells After Intracerebral Transplantation Niclis, Jonathan C. Turner, Christopher Durnall, Jennifer McDougal, Stuart Kauhausen, Jessica A. Leaw, Bryan Dottori, Mirella Parish, Clare L. Thompson, Lachlan H. Stem Cells Transl Med Translational Research Articles and Reviews The capacity for induced pluripotent stem (iPS) cells to be differentiated into a wide range of neural cell types makes them an attractive donor source for autologous neural transplantation therapies aimed at brain repair. Translation to the in vivo setting has been difficult, however, with mixed results in a wide variety of preclinical models of brain injury and limited information on the basic in vivo properties of neural grafts generated from human iPS cells. Here we have generated a human iPS cell line constitutively expressing green fluorescent protein as a basis to identify and characterize grafts resulting from transplantation of neural progenitors into the adult rat brain. The results show that the grafts contain a mix of neural cell types, at various stages of differentiation, including neurons that establish extensive patterns of axonal growth and progressively develop functional properties over the course of 1 year after implantation. These findings form an important basis for the design and interpretation of preclinical studies using human stem cells for functional circuit re‐construction in animal models of brain injury. Stem Cells Translational Medicine 2017;6:1547–1556 John Wiley and Sons Inc. 2017-02-15 /pmc/articles/PMC5689777/ /pubmed/28198124 http://dx.doi.org/10.1002/sctm.16-0198 Text en © 2017 The Authors Stem Cells Translational Medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Translational Research Articles and Reviews
Niclis, Jonathan C.
Turner, Christopher
Durnall, Jennifer
McDougal, Stuart
Kauhausen, Jessica A.
Leaw, Bryan
Dottori, Mirella
Parish, Clare L.
Thompson, Lachlan H.
Long‐Distance Axonal Growth and Protracted Functional Maturation of Neurons Derived from Human Induced Pluripotent Stem Cells After Intracerebral Transplantation
title Long‐Distance Axonal Growth and Protracted Functional Maturation of Neurons Derived from Human Induced Pluripotent Stem Cells After Intracerebral Transplantation
title_full Long‐Distance Axonal Growth and Protracted Functional Maturation of Neurons Derived from Human Induced Pluripotent Stem Cells After Intracerebral Transplantation
title_fullStr Long‐Distance Axonal Growth and Protracted Functional Maturation of Neurons Derived from Human Induced Pluripotent Stem Cells After Intracerebral Transplantation
title_full_unstemmed Long‐Distance Axonal Growth and Protracted Functional Maturation of Neurons Derived from Human Induced Pluripotent Stem Cells After Intracerebral Transplantation
title_short Long‐Distance Axonal Growth and Protracted Functional Maturation of Neurons Derived from Human Induced Pluripotent Stem Cells After Intracerebral Transplantation
title_sort long‐distance axonal growth and protracted functional maturation of neurons derived from human induced pluripotent stem cells after intracerebral transplantation
topic Translational Research Articles and Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689777/
https://www.ncbi.nlm.nih.gov/pubmed/28198124
http://dx.doi.org/10.1002/sctm.16-0198
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