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Combining Injectable Plasma Scaffold with Mesenchymal Stem/Stromal Cells for Repairing Infarct Cavity after Ischemic Stroke
Stroke survivors are typically left with structural brain damage and associated functional impairment in the chronic phase of injury, for which few therapeutic options exist. We reported previously that transplantation of human embryonic stem cell (hESC)-derived neural stem cells together with Matri...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JKL International LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362179/ https://www.ncbi.nlm.nih.gov/pubmed/28400986 http://dx.doi.org/10.14336/AD.2017.0305 |
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author | Zhang, Hongxia Sun, Fen Wang, Jixian Xie, Luokun Yang, Chenqi Pan, Mengxiong Shao, Bei Yang, Guo-Yuan Yang, Shao-Hua ZhuGe, Qichuan Jin, Kunlin |
author_facet | Zhang, Hongxia Sun, Fen Wang, Jixian Xie, Luokun Yang, Chenqi Pan, Mengxiong Shao, Bei Yang, Guo-Yuan Yang, Shao-Hua ZhuGe, Qichuan Jin, Kunlin |
author_sort | Zhang, Hongxia |
collection | PubMed |
description | Stroke survivors are typically left with structural brain damage and associated functional impairment in the chronic phase of injury, for which few therapeutic options exist. We reported previously that transplantation of human embryonic stem cell (hESC)-derived neural stem cells together with Matrigel scaffolding into the brains of rats after focal ischemia reduced infarct volume and improved neurobehavioral performance. Matrigel is a gelatinous protein mixture extracted from mouse sarcoma cells, thus would not be approved for use as a scaffold clinically. In this study, we generated a gel-like scaffold from plasma that was controlled by changing the concentration of CaCl(2). In vitro study confirmed that 10-20 mM CaCl(2) and 10-40% plasma did not affect the viability and proliferation of human and rat bone marrow mesenchymal stem/stromal cells (BMSCs) and neural stem cells (NSCs). We transplanted plasma scaffold in combination of BMSCs into the cystic cavity after focal cerebral ischemia, and found that the atrophy volume was dramatically reduced and motor function was significantly improved in the group transplanted with scaffold/BMSCs compared with the groups treated with vehicle, scaffold or BMSCs only. Our data suggest that plasma-derived scaffold in combination of BMSCs is feasible for tissue engineering approach for the stroke treatment. |
format | Online Article Text |
id | pubmed-5362179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | JKL International LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53621792017-04-12 Combining Injectable Plasma Scaffold with Mesenchymal Stem/Stromal Cells for Repairing Infarct Cavity after Ischemic Stroke Zhang, Hongxia Sun, Fen Wang, Jixian Xie, Luokun Yang, Chenqi Pan, Mengxiong Shao, Bei Yang, Guo-Yuan Yang, Shao-Hua ZhuGe, Qichuan Jin, Kunlin Aging Dis Original Article Stroke survivors are typically left with structural brain damage and associated functional impairment in the chronic phase of injury, for which few therapeutic options exist. We reported previously that transplantation of human embryonic stem cell (hESC)-derived neural stem cells together with Matrigel scaffolding into the brains of rats after focal ischemia reduced infarct volume and improved neurobehavioral performance. Matrigel is a gelatinous protein mixture extracted from mouse sarcoma cells, thus would not be approved for use as a scaffold clinically. In this study, we generated a gel-like scaffold from plasma that was controlled by changing the concentration of CaCl(2). In vitro study confirmed that 10-20 mM CaCl(2) and 10-40% plasma did not affect the viability and proliferation of human and rat bone marrow mesenchymal stem/stromal cells (BMSCs) and neural stem cells (NSCs). We transplanted plasma scaffold in combination of BMSCs into the cystic cavity after focal cerebral ischemia, and found that the atrophy volume was dramatically reduced and motor function was significantly improved in the group transplanted with scaffold/BMSCs compared with the groups treated with vehicle, scaffold or BMSCs only. Our data suggest that plasma-derived scaffold in combination of BMSCs is feasible for tissue engineering approach for the stroke treatment. JKL International LLC 2017-04-01 /pmc/articles/PMC5362179/ /pubmed/28400986 http://dx.doi.org/10.14336/AD.2017.0305 Text en Copyright: © 2017 Zhang, et al. http://creativecommons.org/licenses/by/2.0/ 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 that the original work is properly attributed. |
spellingShingle | Original Article Zhang, Hongxia Sun, Fen Wang, Jixian Xie, Luokun Yang, Chenqi Pan, Mengxiong Shao, Bei Yang, Guo-Yuan Yang, Shao-Hua ZhuGe, Qichuan Jin, Kunlin Combining Injectable Plasma Scaffold with Mesenchymal Stem/Stromal Cells for Repairing Infarct Cavity after Ischemic Stroke |
title | Combining Injectable Plasma Scaffold with Mesenchymal Stem/Stromal Cells for Repairing Infarct Cavity after Ischemic Stroke |
title_full | Combining Injectable Plasma Scaffold with Mesenchymal Stem/Stromal Cells for Repairing Infarct Cavity after Ischemic Stroke |
title_fullStr | Combining Injectable Plasma Scaffold with Mesenchymal Stem/Stromal Cells for Repairing Infarct Cavity after Ischemic Stroke |
title_full_unstemmed | Combining Injectable Plasma Scaffold with Mesenchymal Stem/Stromal Cells for Repairing Infarct Cavity after Ischemic Stroke |
title_short | Combining Injectable Plasma Scaffold with Mesenchymal Stem/Stromal Cells for Repairing Infarct Cavity after Ischemic Stroke |
title_sort | combining injectable plasma scaffold with mesenchymal stem/stromal cells for repairing infarct cavity after ischemic stroke |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362179/ https://www.ncbi.nlm.nih.gov/pubmed/28400986 http://dx.doi.org/10.14336/AD.2017.0305 |
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