author_facet Qian, Yuan
Chen, Xiao‐Xiang
Wang, Wei
Li, Jun‐Jun
Wang, Xian‐Peng
Tang, Zhi‐Wei
Xu, Jiao‐Tian
Lin, Hai
Yang, Zhi‐Yong
Li, Li‐Yan
Song, Xiao‐Bin
Guo, Jia‐Zhi
Bian, Li‐Gong
Zhou, Lei
Lu, Di
Deng, Xing‐Li
Qian, Yuan
Chen, Xiao‐Xiang
Wang, Wei
Li, Jun‐Jun
Wang, Xian‐Peng
Tang, Zhi‐Wei
Xu, Jiao‐Tian
Lin, Hai
Yang, Zhi‐Yong
Li, Li‐Yan
Song, Xiao‐Bin
Guo, Jia‐Zhi
Bian, Li‐Gong
Zhou, Lei
Lu, Di
Deng, Xing‐Li
author Qian, Yuan
Chen, Xiao‐Xiang
Wang, Wei
Li, Jun‐Jun
Wang, Xian‐Peng
Tang, Zhi‐Wei
Xu, Jiao‐Tian
Lin, Hai
Yang, Zhi‐Yong
Li, Li‐Yan
Song, Xiao‐Bin
Guo, Jia‐Zhi
Bian, Li‐Gong
Zhou, Lei
Lu, Di
Deng, Xing‐Li
spellingShingle Qian, Yuan
Chen, Xiao‐Xiang
Wang, Wei
Li, Jun‐Jun
Wang, Xian‐Peng
Tang, Zhi‐Wei
Xu, Jiao‐Tian
Lin, Hai
Yang, Zhi‐Yong
Li, Li‐Yan
Song, Xiao‐Bin
Guo, Jia‐Zhi
Bian, Li‐Gong
Zhou, Lei
Lu, Di
Deng, Xing‐Li
CNS Neuroscience & Therapeutics
Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
Pharmacology (medical)
Physiology (medical)
Psychiatry and Mental health
Pharmacology
author_sort qian, yuan
spelling Qian, Yuan Chen, Xiao‐Xiang Wang, Wei Li, Jun‐Jun Wang, Xian‐Peng Tang, Zhi‐Wei Xu, Jiao‐Tian Lin, Hai Yang, Zhi‐Yong Li, Li‐Yan Song, Xiao‐Bin Guo, Jia‐Zhi Bian, Li‐Gong Zhou, Lei Lu, Di Deng, Xing‐Li 1755-5930 1755-5949 Wiley Pharmacology (medical) Physiology (medical) Psychiatry and Mental health Pharmacology http://dx.doi.org/10.1111/cns.13149 <jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Neural stem cells (NSCs) transplantation is considered a promising treatment for Parkinson's disease. But most NSCs are differentiated into glial cells rather than neurons, and only a few of them survive after transplantation due to the inflammatory environment.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>In this study, neural stem cells (NSCs) and microglial cells both forced with the <jats:italic>Nurr1</jats:italic> gene were transplanted into the striatum of the rat model of PD. The results were evaluated through reverse transcription polymerase chain reaction (RT‐PCR), Western blot, and immunofluorescence analysis.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The behavioral abnormalities of PD rats were improved by combined transplantation of NSCs and microglia, both forced with <jats:italic>Nurr1</jats:italic>. The number of tyrosine hydroxylase+ cells in the striatum of PD rats increased, and the number of Iba1+ cells decreased compared with the other groups. Moreover, the dopamine neurons differentiated from grafted NSCs could still be detected in the striatum of PD rats after 5 months.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>The results suggested that transplantation of Nurr1‐overexpressing NSCs and microglia could improve the inhospitable host brain environments, which will be a new potential strategy for the cell replacement therapy in PD.</jats:p></jats:sec> Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats CNS Neuroscience & Therapeutics
doi_str_mv 10.1111/cns.13149
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Medizin
Psychologie
Chemie und Pharmazie
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imprint_str_mv Wiley, 2020
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recordtype ai
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series CNS Neuroscience & Therapeutics
source_id 49
title Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_unstemmed Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_full Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_fullStr Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_full_unstemmed Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_short Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_sort transplantation of nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
topic Pharmacology (medical)
Physiology (medical)
Psychiatry and Mental health
Pharmacology
url http://dx.doi.org/10.1111/cns.13149
publishDate 2020
physical 55-65
description <jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Neural stem cells (NSCs) transplantation is considered a promising treatment for Parkinson's disease. But most NSCs are differentiated into glial cells rather than neurons, and only a few of them survive after transplantation due to the inflammatory environment.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>In this study, neural stem cells (NSCs) and microglial cells both forced with the <jats:italic>Nurr1</jats:italic> gene were transplanted into the striatum of the rat model of PD. The results were evaluated through reverse transcription polymerase chain reaction (RT‐PCR), Western blot, and immunofluorescence analysis.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The behavioral abnormalities of PD rats were improved by combined transplantation of NSCs and microglia, both forced with <jats:italic>Nurr1</jats:italic>. The number of tyrosine hydroxylase+ cells in the striatum of PD rats increased, and the number of Iba1+ cells decreased compared with the other groups. Moreover, the dopamine neurons differentiated from grafted NSCs could still be detected in the striatum of PD rats after 5 months.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>The results suggested that transplantation of Nurr1‐overexpressing NSCs and microglia could improve the inhospitable host brain environments, which will be  a new potential strategy for the cell replacement therapy in PD.</jats:p></jats:sec>
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author Qian, Yuan, Chen, Xiao‐Xiang, Wang, Wei, Li, Jun‐Jun, Wang, Xian‐Peng, Tang, Zhi‐Wei, Xu, Jiao‐Tian, Lin, Hai, Yang, Zhi‐Yong, Li, Li‐Yan, Song, Xiao‐Bin, Guo, Jia‐Zhi, Bian, Li‐Gong, Zhou, Lei, Lu, Di, Deng, Xing‐Li
author_facet Qian, Yuan, Chen, Xiao‐Xiang, Wang, Wei, Li, Jun‐Jun, Wang, Xian‐Peng, Tang, Zhi‐Wei, Xu, Jiao‐Tian, Lin, Hai, Yang, Zhi‐Yong, Li, Li‐Yan, Song, Xiao‐Bin, Guo, Jia‐Zhi, Bian, Li‐Gong, Zhou, Lei, Lu, Di, Deng, Xing‐Li, Qian, Yuan, Chen, Xiao‐Xiang, Wang, Wei, Li, Jun‐Jun, Wang, Xian‐Peng, Tang, Zhi‐Wei, Xu, Jiao‐Tian, Lin, Hai, Yang, Zhi‐Yong, Li, Li‐Yan, Song, Xiao‐Bin, Guo, Jia‐Zhi, Bian, Li‐Gong, Zhou, Lei, Lu, Di, Deng, Xing‐Li
author_sort qian, yuan
container_issue 1
container_start_page 55
container_title CNS Neuroscience & Therapeutics
container_volume 26
description <jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Neural stem cells (NSCs) transplantation is considered a promising treatment for Parkinson's disease. But most NSCs are differentiated into glial cells rather than neurons, and only a few of them survive after transplantation due to the inflammatory environment.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>In this study, neural stem cells (NSCs) and microglial cells both forced with the <jats:italic>Nurr1</jats:italic> gene were transplanted into the striatum of the rat model of PD. The results were evaluated through reverse transcription polymerase chain reaction (RT‐PCR), Western blot, and immunofluorescence analysis.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The behavioral abnormalities of PD rats were improved by combined transplantation of NSCs and microglia, both forced with <jats:italic>Nurr1</jats:italic>. The number of tyrosine hydroxylase+ cells in the striatum of PD rats increased, and the number of Iba1+ cells decreased compared with the other groups. Moreover, the dopamine neurons differentiated from grafted NSCs could still be detected in the striatum of PD rats after 5 months.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>The results suggested that transplantation of Nurr1‐overexpressing NSCs and microglia could improve the inhospitable host brain environments, which will be  a new potential strategy for the cell replacement therapy in PD.</jats:p></jats:sec>
doi_str_mv 10.1111/cns.13149
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id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTExMS9jbnMuMTMxNDk
imprint Wiley, 2020
imprint_str_mv Wiley, 2020
institution DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-D161, DE-Zwi2, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14
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spelling Qian, Yuan Chen, Xiao‐Xiang Wang, Wei Li, Jun‐Jun Wang, Xian‐Peng Tang, Zhi‐Wei Xu, Jiao‐Tian Lin, Hai Yang, Zhi‐Yong Li, Li‐Yan Song, Xiao‐Bin Guo, Jia‐Zhi Bian, Li‐Gong Zhou, Lei Lu, Di Deng, Xing‐Li 1755-5930 1755-5949 Wiley Pharmacology (medical) Physiology (medical) Psychiatry and Mental health Pharmacology http://dx.doi.org/10.1111/cns.13149 <jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Neural stem cells (NSCs) transplantation is considered a promising treatment for Parkinson's disease. But most NSCs are differentiated into glial cells rather than neurons, and only a few of them survive after transplantation due to the inflammatory environment.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>In this study, neural stem cells (NSCs) and microglial cells both forced with the <jats:italic>Nurr1</jats:italic> gene were transplanted into the striatum of the rat model of PD. The results were evaluated through reverse transcription polymerase chain reaction (RT‐PCR), Western blot, and immunofluorescence analysis.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>The behavioral abnormalities of PD rats were improved by combined transplantation of NSCs and microglia, both forced with <jats:italic>Nurr1</jats:italic>. The number of tyrosine hydroxylase+ cells in the striatum of PD rats increased, and the number of Iba1+ cells decreased compared with the other groups. Moreover, the dopamine neurons differentiated from grafted NSCs could still be detected in the striatum of PD rats after 5 months.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>The results suggested that transplantation of Nurr1‐overexpressing NSCs and microglia could improve the inhospitable host brain environments, which will be a new potential strategy for the cell replacement therapy in PD.</jats:p></jats:sec> Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats CNS Neuroscience & Therapeutics
spellingShingle Qian, Yuan, Chen, Xiao‐Xiang, Wang, Wei, Li, Jun‐Jun, Wang, Xian‐Peng, Tang, Zhi‐Wei, Xu, Jiao‐Tian, Lin, Hai, Yang, Zhi‐Yong, Li, Li‐Yan, Song, Xiao‐Bin, Guo, Jia‐Zhi, Bian, Li‐Gong, Zhou, Lei, Lu, Di, Deng, Xing‐Li, CNS Neuroscience & Therapeutics, Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats, Pharmacology (medical), Physiology (medical), Psychiatry and Mental health, Pharmacology
title Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_full Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_fullStr Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_full_unstemmed Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_short Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_sort transplantation of nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
title_unstemmed Transplantation of Nurr1‐overexpressing neural stem cells and microglia for treating parkinsonian rats
topic Pharmacology (medical), Physiology (medical), Psychiatry and Mental health, Pharmacology
url http://dx.doi.org/10.1111/cns.13149