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Intravenous Administration of Adipose-Derived Stem Cell Protein Extracts Improves Neurological Deficits in a Rat Model of Stroke

Treatment of adipose-derived stem cell (ADSC) substantially improves the neurological deficits during stroke by reducing neuronal injury, limiting proinflammatory immune responses, and promoting neuronal repair, which makes ADSC-based therapy an attractive approach for treating stroke. However, the...

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Autores principales: Zhao, Kai, Li, Rui, Gu, Changcong, Liu, Long, Jia, Yulong, Guo, Xize, Zhang, Wanping, Pei, Chunying, Tian, Linlu, Li, Bo, Jia, Jianrong, Cheng, Huakun, Xu, Hongwei, Li, Lixian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318632/
https://www.ncbi.nlm.nih.gov/pubmed/28265288
http://dx.doi.org/10.1155/2017/2153629
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author Zhao, Kai
Li, Rui
Gu, Changcong
Liu, Long
Jia, Yulong
Guo, Xize
Zhang, Wanping
Pei, Chunying
Tian, Linlu
Li, Bo
Jia, Jianrong
Cheng, Huakun
Xu, Hongwei
Li, Lixian
author_facet Zhao, Kai
Li, Rui
Gu, Changcong
Liu, Long
Jia, Yulong
Guo, Xize
Zhang, Wanping
Pei, Chunying
Tian, Linlu
Li, Bo
Jia, Jianrong
Cheng, Huakun
Xu, Hongwei
Li, Lixian
author_sort Zhao, Kai
collection PubMed
description Treatment of adipose-derived stem cell (ADSC) substantially improves the neurological deficits during stroke by reducing neuronal injury, limiting proinflammatory immune responses, and promoting neuronal repair, which makes ADSC-based therapy an attractive approach for treating stroke. However, the potential risk of tumorigenicity and low survival rate of the implanted cells limit the clinical use of ADSC. Cell-free extracts from ADSC (ADSC-E) may be a feasible approach that could overcome these limitations. Here, we aim to explore the potential usage of ADSC-E in treating rat transient middle cerebral artery occlusion (tMCAO). We demonstrated that intravenous (IV) injection of ADSC-E remarkably reduces the ischemic lesion and number of apoptotic neurons as compared to other control groups. Although ADSC and ADSC-E treatment results in a similar degree of a long-term clinical beneficial outcome, the dynamics between two ADSC-based therapies are different. While the injection of ADSC leads to a relatively mild but prolonged therapeutic effect, the administration of ADSC-E results in a fast and pronounced clinical improvement which was associated with a unique change in the molecular signature suggesting that potential mechanisms underlying different therapeutic approach may be different. Together these data provide translational evidence for using protein extracts from ADSC for treating stroke.
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spelling pubmed-53186322017-03-06 Intravenous Administration of Adipose-Derived Stem Cell Protein Extracts Improves Neurological Deficits in a Rat Model of Stroke Zhao, Kai Li, Rui Gu, Changcong Liu, Long Jia, Yulong Guo, Xize Zhang, Wanping Pei, Chunying Tian, Linlu Li, Bo Jia, Jianrong Cheng, Huakun Xu, Hongwei Li, Lixian Stem Cells Int Research Article Treatment of adipose-derived stem cell (ADSC) substantially improves the neurological deficits during stroke by reducing neuronal injury, limiting proinflammatory immune responses, and promoting neuronal repair, which makes ADSC-based therapy an attractive approach for treating stroke. However, the potential risk of tumorigenicity and low survival rate of the implanted cells limit the clinical use of ADSC. Cell-free extracts from ADSC (ADSC-E) may be a feasible approach that could overcome these limitations. Here, we aim to explore the potential usage of ADSC-E in treating rat transient middle cerebral artery occlusion (tMCAO). We demonstrated that intravenous (IV) injection of ADSC-E remarkably reduces the ischemic lesion and number of apoptotic neurons as compared to other control groups. Although ADSC and ADSC-E treatment results in a similar degree of a long-term clinical beneficial outcome, the dynamics between two ADSC-based therapies are different. While the injection of ADSC leads to a relatively mild but prolonged therapeutic effect, the administration of ADSC-E results in a fast and pronounced clinical improvement which was associated with a unique change in the molecular signature suggesting that potential mechanisms underlying different therapeutic approach may be different. Together these data provide translational evidence for using protein extracts from ADSC for treating stroke. Hindawi Publishing Corporation 2017 2017-02-07 /pmc/articles/PMC5318632/ /pubmed/28265288 http://dx.doi.org/10.1155/2017/2153629 Text en Copyright © 2017 Kai Zhao et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhao, Kai
Li, Rui
Gu, Changcong
Liu, Long
Jia, Yulong
Guo, Xize
Zhang, Wanping
Pei, Chunying
Tian, Linlu
Li, Bo
Jia, Jianrong
Cheng, Huakun
Xu, Hongwei
Li, Lixian
Intravenous Administration of Adipose-Derived Stem Cell Protein Extracts Improves Neurological Deficits in a Rat Model of Stroke
title Intravenous Administration of Adipose-Derived Stem Cell Protein Extracts Improves Neurological Deficits in a Rat Model of Stroke
title_full Intravenous Administration of Adipose-Derived Stem Cell Protein Extracts Improves Neurological Deficits in a Rat Model of Stroke
title_fullStr Intravenous Administration of Adipose-Derived Stem Cell Protein Extracts Improves Neurological Deficits in a Rat Model of Stroke
title_full_unstemmed Intravenous Administration of Adipose-Derived Stem Cell Protein Extracts Improves Neurological Deficits in a Rat Model of Stroke
title_short Intravenous Administration of Adipose-Derived Stem Cell Protein Extracts Improves Neurological Deficits in a Rat Model of Stroke
title_sort intravenous administration of adipose-derived stem cell protein extracts improves neurological deficits in a rat model of stroke
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318632/
https://www.ncbi.nlm.nih.gov/pubmed/28265288
http://dx.doi.org/10.1155/2017/2153629
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