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Transplantation of Induced Pluripotent Stem Cells Improves Functional Recovery in Huntington's Disease Rat Model
The purpose of this study was to determine the functional recovery of the transplanted induced pluripotent stem cells in a rat model of Huntington's disease with use of (18)F-FDG microPET/CT imaging. METHODS: In a quinolinic acid-induced rat model of striatal degeneration, induced pluripotent s...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108311/ https://www.ncbi.nlm.nih.gov/pubmed/25054283 http://dx.doi.org/10.1371/journal.pone.0101185 |
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author | Mu, Shuhua Wang, Jiachuan Zhou, Guangqian Peng, Wenda He, Zhendan Zhao, Zhenfu Mo, CuiPing Qu, Junle Zhang, Jian |
author_facet | Mu, Shuhua Wang, Jiachuan Zhou, Guangqian Peng, Wenda He, Zhendan Zhao, Zhenfu Mo, CuiPing Qu, Junle Zhang, Jian |
author_sort | Mu, Shuhua |
collection | PubMed |
description | The purpose of this study was to determine the functional recovery of the transplanted induced pluripotent stem cells in a rat model of Huntington's disease with use of (18)F-FDG microPET/CT imaging. METHODS: In a quinolinic acid-induced rat model of striatal degeneration, induced pluripotent stem cells were transplanted into the ipsilateral lateral ventricle ten days after the quinolinic acid injection. The response to the treatment was evaluated by serial (18)F-FDG PET/CT scans and Morris water maze test. Histological analyses and Western blotting were performed six weeks after stem cell transplantation. RESULTS: After induced pluripotent stem cells transplantation, higher (18)F-FDG accumulation in the injured striatum was observed during the 4 to 6-weeks period compared with the quinolinic acid-injected group, suggesting the metabolic recovery of injured striatum. The induced pluripotent stem cells transplantation improved learning and memory function (and striatal atrophy) of the rat in six week in the comparison with the quinolinic acid-treated controls. In addition, immunohistochemical analysis demonstrated that transplanted stem cells survived and migrated into the lesioned area in striatum, and most of the stem cells expressed protein markers of neurons and glial cells. CONCLUSION: Our findings show that induced pluripotent stem cells can survive, differentiate to functional neurons and improve partial striatal function and metabolism after implantation in a rat Huntington's disease model. |
format | Online Article Text |
id | pubmed-4108311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41083112014-07-24 Transplantation of Induced Pluripotent Stem Cells Improves Functional Recovery in Huntington's Disease Rat Model Mu, Shuhua Wang, Jiachuan Zhou, Guangqian Peng, Wenda He, Zhendan Zhao, Zhenfu Mo, CuiPing Qu, Junle Zhang, Jian PLoS One Research Article The purpose of this study was to determine the functional recovery of the transplanted induced pluripotent stem cells in a rat model of Huntington's disease with use of (18)F-FDG microPET/CT imaging. METHODS: In a quinolinic acid-induced rat model of striatal degeneration, induced pluripotent stem cells were transplanted into the ipsilateral lateral ventricle ten days after the quinolinic acid injection. The response to the treatment was evaluated by serial (18)F-FDG PET/CT scans and Morris water maze test. Histological analyses and Western blotting were performed six weeks after stem cell transplantation. RESULTS: After induced pluripotent stem cells transplantation, higher (18)F-FDG accumulation in the injured striatum was observed during the 4 to 6-weeks period compared with the quinolinic acid-injected group, suggesting the metabolic recovery of injured striatum. The induced pluripotent stem cells transplantation improved learning and memory function (and striatal atrophy) of the rat in six week in the comparison with the quinolinic acid-treated controls. In addition, immunohistochemical analysis demonstrated that transplanted stem cells survived and migrated into the lesioned area in striatum, and most of the stem cells expressed protein markers of neurons and glial cells. CONCLUSION: Our findings show that induced pluripotent stem cells can survive, differentiate to functional neurons and improve partial striatal function and metabolism after implantation in a rat Huntington's disease model. Public Library of Science 2014-07-23 /pmc/articles/PMC4108311/ /pubmed/25054283 http://dx.doi.org/10.1371/journal.pone.0101185 Text en © 2014 Mu et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Mu, Shuhua Wang, Jiachuan Zhou, Guangqian Peng, Wenda He, Zhendan Zhao, Zhenfu Mo, CuiPing Qu, Junle Zhang, Jian Transplantation of Induced Pluripotent Stem Cells Improves Functional Recovery in Huntington's Disease Rat Model |
title | Transplantation of Induced Pluripotent Stem Cells Improves Functional Recovery in Huntington's Disease Rat Model |
title_full | Transplantation of Induced Pluripotent Stem Cells Improves Functional Recovery in Huntington's Disease Rat Model |
title_fullStr | Transplantation of Induced Pluripotent Stem Cells Improves Functional Recovery in Huntington's Disease Rat Model |
title_full_unstemmed | Transplantation of Induced Pluripotent Stem Cells Improves Functional Recovery in Huntington's Disease Rat Model |
title_short | Transplantation of Induced Pluripotent Stem Cells Improves Functional Recovery in Huntington's Disease Rat Model |
title_sort | transplantation of induced pluripotent stem cells improves functional recovery in huntington's disease rat model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108311/ https://www.ncbi.nlm.nih.gov/pubmed/25054283 http://dx.doi.org/10.1371/journal.pone.0101185 |
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