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Induced Pluripotent Stem Cell-Derived Neural Stem Cell Therapy Enhances Recovery in an Ischemic Stroke Pig Model

Induced pluripotent stem cell-derived neural stem cells (iNSCs) have significant potential as an autologous, multifunctional cell therapy for stroke, which is the primary cause of long term disability in the United States and the second leading cause of death worldwide. Here we show that iNSC transp...

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Autores principales: Baker, Emily W., Platt, Simon R., Lau, Vivian W., Grace, Harrison E., Holmes, Shannon P., Wang, Liya, Duberstein, Kylee Jo, Howerth, Elizabeth W., Kinder, Holly A., Stice, Steve L., Hess, David C., Mao, Hui, West, Franklin D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577218/
https://www.ncbi.nlm.nih.gov/pubmed/28855627
http://dx.doi.org/10.1038/s41598-017-10406-x
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author Baker, Emily W.
Platt, Simon R.
Lau, Vivian W.
Grace, Harrison E.
Holmes, Shannon P.
Wang, Liya
Duberstein, Kylee Jo
Howerth, Elizabeth W.
Kinder, Holly A.
Stice, Steve L.
Hess, David C.
Mao, Hui
West, Franklin D.
author_facet Baker, Emily W.
Platt, Simon R.
Lau, Vivian W.
Grace, Harrison E.
Holmes, Shannon P.
Wang, Liya
Duberstein, Kylee Jo
Howerth, Elizabeth W.
Kinder, Holly A.
Stice, Steve L.
Hess, David C.
Mao, Hui
West, Franklin D.
author_sort Baker, Emily W.
collection PubMed
description Induced pluripotent stem cell-derived neural stem cells (iNSCs) have significant potential as an autologous, multifunctional cell therapy for stroke, which is the primary cause of long term disability in the United States and the second leading cause of death worldwide. Here we show that iNSC transplantation improves recovery through neuroprotective, regenerative, and cell replacement mechanisms in a novel ischemic pig stroke model. Longitudinal multiparametric magnetic resonance imaging (MRI) following iNSC therapy demonstrated reduced changes in white matter integrity, cerebral blood perfusion, and brain metabolism in the infarcted tissue. The observed tissue level recovery strongly correlated with decreased immune response, enhanced neuronal protection, and increased neurogenesis. iNSCs differentiated into neurons and oligodendrocytes with indication of long term integration. The robust recovery response to iNSC therapy in a translational pig stroke model with increased predictive potential strongly supports that iNSCs may be the critically needed therapeutic for human stroke patients.
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spelling pubmed-55772182017-09-01 Induced Pluripotent Stem Cell-Derived Neural Stem Cell Therapy Enhances Recovery in an Ischemic Stroke Pig Model Baker, Emily W. Platt, Simon R. Lau, Vivian W. Grace, Harrison E. Holmes, Shannon P. Wang, Liya Duberstein, Kylee Jo Howerth, Elizabeth W. Kinder, Holly A. Stice, Steve L. Hess, David C. Mao, Hui West, Franklin D. Sci Rep Article Induced pluripotent stem cell-derived neural stem cells (iNSCs) have significant potential as an autologous, multifunctional cell therapy for stroke, which is the primary cause of long term disability in the United States and the second leading cause of death worldwide. Here we show that iNSC transplantation improves recovery through neuroprotective, regenerative, and cell replacement mechanisms in a novel ischemic pig stroke model. Longitudinal multiparametric magnetic resonance imaging (MRI) following iNSC therapy demonstrated reduced changes in white matter integrity, cerebral blood perfusion, and brain metabolism in the infarcted tissue. The observed tissue level recovery strongly correlated with decreased immune response, enhanced neuronal protection, and increased neurogenesis. iNSCs differentiated into neurons and oligodendrocytes with indication of long term integration. The robust recovery response to iNSC therapy in a translational pig stroke model with increased predictive potential strongly supports that iNSCs may be the critically needed therapeutic for human stroke patients. Nature Publishing Group UK 2017-08-30 /pmc/articles/PMC5577218/ /pubmed/28855627 http://dx.doi.org/10.1038/s41598-017-10406-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Baker, Emily W.
Platt, Simon R.
Lau, Vivian W.
Grace, Harrison E.
Holmes, Shannon P.
Wang, Liya
Duberstein, Kylee Jo
Howerth, Elizabeth W.
Kinder, Holly A.
Stice, Steve L.
Hess, David C.
Mao, Hui
West, Franklin D.
Induced Pluripotent Stem Cell-Derived Neural Stem Cell Therapy Enhances Recovery in an Ischemic Stroke Pig Model
title Induced Pluripotent Stem Cell-Derived Neural Stem Cell Therapy Enhances Recovery in an Ischemic Stroke Pig Model
title_full Induced Pluripotent Stem Cell-Derived Neural Stem Cell Therapy Enhances Recovery in an Ischemic Stroke Pig Model
title_fullStr Induced Pluripotent Stem Cell-Derived Neural Stem Cell Therapy Enhances Recovery in an Ischemic Stroke Pig Model
title_full_unstemmed Induced Pluripotent Stem Cell-Derived Neural Stem Cell Therapy Enhances Recovery in an Ischemic Stroke Pig Model
title_short Induced Pluripotent Stem Cell-Derived Neural Stem Cell Therapy Enhances Recovery in an Ischemic Stroke Pig Model
title_sort induced pluripotent stem cell-derived neural stem cell therapy enhances recovery in an ischemic stroke pig model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577218/
https://www.ncbi.nlm.nih.gov/pubmed/28855627
http://dx.doi.org/10.1038/s41598-017-10406-x
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