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Pretreatment of Adipose Derived Stem Cells with Curcumin Facilitates Myocardial Recovery via Antiapoptosis and Angiogenesis

The poor survival rate of transplanted stem cells in ischemic myocardium has limited their therapeutic efficacy. Curcumin has potent antioxidant property. This study investigates whether prior curcumin treatment protects stem cells from oxidative stress injury and improves myocardial recovery follow...

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Autores principales: Liu, Jianfeng, Zhu, Ping, Song, Peng, Xiong, Weiping, Chen, Haixu, Peng, Wenhui, Wang, Shuxia, Li, Shan, Fu, Zhiqing, Wang, Yutang, Wang, Haibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436501/
https://www.ncbi.nlm.nih.gov/pubmed/26074974
http://dx.doi.org/10.1155/2015/638153
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author Liu, Jianfeng
Zhu, Ping
Song, Peng
Xiong, Weiping
Chen, Haixu
Peng, Wenhui
Wang, Shuxia
Li, Shan
Fu, Zhiqing
Wang, Yutang
Wang, Haibin
author_facet Liu, Jianfeng
Zhu, Ping
Song, Peng
Xiong, Weiping
Chen, Haixu
Peng, Wenhui
Wang, Shuxia
Li, Shan
Fu, Zhiqing
Wang, Yutang
Wang, Haibin
author_sort Liu, Jianfeng
collection PubMed
description The poor survival rate of transplanted stem cells in ischemic myocardium has limited their therapeutic efficacy. Curcumin has potent antioxidant property. This study investigates whether prior curcumin treatment protects stem cells from oxidative stress injury and improves myocardial recovery following cells transplantation. Autologous Sprague-Dawley rat adipose derived mesenchymal stem cells (ADSCs) were pretreated with or without curcumin. The hydrogen peroxide/serum deprivation (H(2)O(2)/SD) medium was used to mimic the ischemic condition in vitro. Cytoprotective effects of curcumin on ADSCs were evaluated. Curcumin pretreatment significantly increased cell viability and VEGF secretion, and decreased cell injury and apoptosis via regulation of PTEN/Akt/p53 and HO-1 signal proteins expression. The therapeutic potential of ADSCs implantation was investigated in myocardial ischemia-reperfusion injury (IRI) model. Transplantation of curcumin pretreated ADSCs not only resulted in better heart function, higher cells retention, and smaller infarct size, but also decreased myocardial apoptosis, promoted neovascularization, and increased VEGF level in ischemic myocardium. Together, priming of ADSCs with curcumin improved tolerance to oxidative stress injury and resulted in enhancement of their therapeutic potential of ADSCs for myocardial repair. Curcumin pretreatment is a promising adjuvant strategy for stem cells transplantation in myocardial restoration.
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spelling pubmed-44365012015-06-14 Pretreatment of Adipose Derived Stem Cells with Curcumin Facilitates Myocardial Recovery via Antiapoptosis and Angiogenesis Liu, Jianfeng Zhu, Ping Song, Peng Xiong, Weiping Chen, Haixu Peng, Wenhui Wang, Shuxia Li, Shan Fu, Zhiqing Wang, Yutang Wang, Haibin Stem Cells Int Research Article The poor survival rate of transplanted stem cells in ischemic myocardium has limited their therapeutic efficacy. Curcumin has potent antioxidant property. This study investigates whether prior curcumin treatment protects stem cells from oxidative stress injury and improves myocardial recovery following cells transplantation. Autologous Sprague-Dawley rat adipose derived mesenchymal stem cells (ADSCs) were pretreated with or without curcumin. The hydrogen peroxide/serum deprivation (H(2)O(2)/SD) medium was used to mimic the ischemic condition in vitro. Cytoprotective effects of curcumin on ADSCs were evaluated. Curcumin pretreatment significantly increased cell viability and VEGF secretion, and decreased cell injury and apoptosis via regulation of PTEN/Akt/p53 and HO-1 signal proteins expression. The therapeutic potential of ADSCs implantation was investigated in myocardial ischemia-reperfusion injury (IRI) model. Transplantation of curcumin pretreated ADSCs not only resulted in better heart function, higher cells retention, and smaller infarct size, but also decreased myocardial apoptosis, promoted neovascularization, and increased VEGF level in ischemic myocardium. Together, priming of ADSCs with curcumin improved tolerance to oxidative stress injury and resulted in enhancement of their therapeutic potential of ADSCs for myocardial repair. Curcumin pretreatment is a promising adjuvant strategy for stem cells transplantation in myocardial restoration. Hindawi Publishing Corporation 2015 2015-05-05 /pmc/articles/PMC4436501/ /pubmed/26074974 http://dx.doi.org/10.1155/2015/638153 Text en Copyright © 2015 Jianfeng Liu et al. https://creativecommons.org/licenses/by/3.0/ 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
Liu, Jianfeng
Zhu, Ping
Song, Peng
Xiong, Weiping
Chen, Haixu
Peng, Wenhui
Wang, Shuxia
Li, Shan
Fu, Zhiqing
Wang, Yutang
Wang, Haibin
Pretreatment of Adipose Derived Stem Cells with Curcumin Facilitates Myocardial Recovery via Antiapoptosis and Angiogenesis
title Pretreatment of Adipose Derived Stem Cells with Curcumin Facilitates Myocardial Recovery via Antiapoptosis and Angiogenesis
title_full Pretreatment of Adipose Derived Stem Cells with Curcumin Facilitates Myocardial Recovery via Antiapoptosis and Angiogenesis
title_fullStr Pretreatment of Adipose Derived Stem Cells with Curcumin Facilitates Myocardial Recovery via Antiapoptosis and Angiogenesis
title_full_unstemmed Pretreatment of Adipose Derived Stem Cells with Curcumin Facilitates Myocardial Recovery via Antiapoptosis and Angiogenesis
title_short Pretreatment of Adipose Derived Stem Cells with Curcumin Facilitates Myocardial Recovery via Antiapoptosis and Angiogenesis
title_sort pretreatment of adipose derived stem cells with curcumin facilitates myocardial recovery via antiapoptosis and angiogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436501/
https://www.ncbi.nlm.nih.gov/pubmed/26074974
http://dx.doi.org/10.1155/2015/638153
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