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Effects of primary microglia and astrocytes on neural stem cells in in vitro and in vivo models of ischemic stroke
Transplantation of neural stem cells (NSCs) can protect neurons in animal stroke models; however, their low rates of survival and neuronal differentiation limit their clinical application. Glial niches, an important location of neural stem cells, regulate survival, proliferation and differentiation...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8328755/ https://www.ncbi.nlm.nih.gov/pubmed/33510055 http://dx.doi.org/10.4103/1673-5374.306093 |
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author | Wen, Sheng-Jun Zheng, Xi-Min Liu, Li-Fen Li, Na-Na Mao, Hai-An Huang, Liang Yuan, Qiong-Lan |
author_facet | Wen, Sheng-Jun Zheng, Xi-Min Liu, Li-Fen Li, Na-Na Mao, Hai-An Huang, Liang Yuan, Qiong-Lan |
author_sort | Wen, Sheng-Jun |
collection | PubMed |
description | Transplantation of neural stem cells (NSCs) can protect neurons in animal stroke models; however, their low rates of survival and neuronal differentiation limit their clinical application. Glial niches, an important location of neural stem cells, regulate survival, proliferation and differentiation of neural stem cells. However, the effects of activated glial cells on neural stem cells remain unclear. In the present study, we explored the effects of activated astrocytes and microglia on neural stem cells in vitro stroke models. We also investigated the effects of combined transplantation of neural stem cells and glial cells after stroke in rats. In a Transwell co-culture system, primary cultured astrocytes, microglia or mixed glial cells were exposed to glutamate or H(2)O(2) and then seeded in the upper inserts, while primary neural stem cells were seeded in the lower uncoated wells and cultured for 7 days. Our results showed that microglia were conducive to neurosphere formation and had no effects on apoptosis within neurospheres, while astrocytes and mixed glial cells were conducive to neurosphere differentiation and reduced apoptosis within neurospheres, regardless of their pretreatment. In contrast, microglia and astrocytes induced neuronal differentiation of neural stem cells in differentiation medium, regardless of their pretreatment, with an exception of astrocytes pretreated with H(2)O(2). Rat models of ischemic stroke were established by occlusion of the middle cerebral artery. Three days later, 5 × 10(5) neural stem cells with microglia or astrocytes were injected into the right lateral ventricle. Neural stem cell/astrocyte-treated rats displayed better improvement of neurological deficits than neural stem cell only-treated rats at 4 days after cell transplantation. Moreover, neural stem cell/microglia-, and neural stem cell/astrocyte-treated rats showed a significant decrease in ischemic volume compared with neural stem cell-treated rats. These findings indicate that microglia and astrocytes exert different effects on neural stem cells, and that co-transplantation of neural stem cells and astrocytes is more conducive to the recovery of neurological impairment in rats with ischemic stroke. The study was approved by the Animal Ethics Committee of Tongji University School of Medicine, China (approval No. 2010-TJAA08220401) in 2010. |
format | Online Article Text |
id | pubmed-8328755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-83287552021-08-09 Effects of primary microglia and astrocytes on neural stem cells in in vitro and in vivo models of ischemic stroke Wen, Sheng-Jun Zheng, Xi-Min Liu, Li-Fen Li, Na-Na Mao, Hai-An Huang, Liang Yuan, Qiong-Lan Neural Regen Res Research Article Transplantation of neural stem cells (NSCs) can protect neurons in animal stroke models; however, their low rates of survival and neuronal differentiation limit their clinical application. Glial niches, an important location of neural stem cells, regulate survival, proliferation and differentiation of neural stem cells. However, the effects of activated glial cells on neural stem cells remain unclear. In the present study, we explored the effects of activated astrocytes and microglia on neural stem cells in vitro stroke models. We also investigated the effects of combined transplantation of neural stem cells and glial cells after stroke in rats. In a Transwell co-culture system, primary cultured astrocytes, microglia or mixed glial cells were exposed to glutamate or H(2)O(2) and then seeded in the upper inserts, while primary neural stem cells were seeded in the lower uncoated wells and cultured for 7 days. Our results showed that microglia were conducive to neurosphere formation and had no effects on apoptosis within neurospheres, while astrocytes and mixed glial cells were conducive to neurosphere differentiation and reduced apoptosis within neurospheres, regardless of their pretreatment. In contrast, microglia and astrocytes induced neuronal differentiation of neural stem cells in differentiation medium, regardless of their pretreatment, with an exception of astrocytes pretreated with H(2)O(2). Rat models of ischemic stroke were established by occlusion of the middle cerebral artery. Three days later, 5 × 10(5) neural stem cells with microglia or astrocytes were injected into the right lateral ventricle. Neural stem cell/astrocyte-treated rats displayed better improvement of neurological deficits than neural stem cell only-treated rats at 4 days after cell transplantation. Moreover, neural stem cell/microglia-, and neural stem cell/astrocyte-treated rats showed a significant decrease in ischemic volume compared with neural stem cell-treated rats. These findings indicate that microglia and astrocytes exert different effects on neural stem cells, and that co-transplantation of neural stem cells and astrocytes is more conducive to the recovery of neurological impairment in rats with ischemic stroke. The study was approved by the Animal Ethics Committee of Tongji University School of Medicine, China (approval No. 2010-TJAA08220401) in 2010. Wolters Kluwer - Medknow 2021-01-25 /pmc/articles/PMC8328755/ /pubmed/33510055 http://dx.doi.org/10.4103/1673-5374.306093 Text en Copyright: © 2021 Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Wen, Sheng-Jun Zheng, Xi-Min Liu, Li-Fen Li, Na-Na Mao, Hai-An Huang, Liang Yuan, Qiong-Lan Effects of primary microglia and astrocytes on neural stem cells in in vitro and in vivo models of ischemic stroke |
title | Effects of primary microglia and astrocytes on neural stem cells in in vitro and in vivo models of ischemic stroke |
title_full | Effects of primary microglia and astrocytes on neural stem cells in in vitro and in vivo models of ischemic stroke |
title_fullStr | Effects of primary microglia and astrocytes on neural stem cells in in vitro and in vivo models of ischemic stroke |
title_full_unstemmed | Effects of primary microglia and astrocytes on neural stem cells in in vitro and in vivo models of ischemic stroke |
title_short | Effects of primary microglia and astrocytes on neural stem cells in in vitro and in vivo models of ischemic stroke |
title_sort | effects of primary microglia and astrocytes on neural stem cells in in vitro and in vivo models of ischemic stroke |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8328755/ https://www.ncbi.nlm.nih.gov/pubmed/33510055 http://dx.doi.org/10.4103/1673-5374.306093 |
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