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Effects of heme oxygenase-1 gene modulated mesenchymal stem cells on vasculogenesis in ischemic swine hearts

JIANG Yi-bo ZHANG Xiao-li TANG Yao-liang MA Gen-shan SHEN Cheng-xing WEI Qin ZHU Qi YAO Yu-yu LIU Nai-feng

中华医学杂志(英文版)2011,Vol.124Issue(3):401-407,7.
中华医学杂志(英文版)2011,Vol.124Issue(3):401-407,7.DOI:10.3760/cma.j.issn.0366-6999.2011.03.015

Effects of heme oxygenase-1 gene modulated mesenchymal stem cells on vasculogenesis in ischemic swine hearts

Effects of heme oxygenase-1 gene modulated mesenchymal stem cells on vasculogenesis in ischemic swine hearts

JIANG Yi-bo 1ZHANG Xiao-li 1TANG Yao-liang 2MA Gen-shan 1SHEN Cheng-xing 1WEI Qin 1ZHU Qi 1YAO Yu-yu 1LIU Nai-feng1

作者信息

  • 1. Department of Cardiology, Zhongda Hospital, Southeast University, Nanjing, Jiangsu 210009, China
  • 2. Division of Cardiovascular Diseases, University of Cincinnati, 231 Albert Sabin Way, ML 0542, Cincinnati, OH 45267-0542, USA
  • 折叠

摘要

Abstract

Background Mesenchymal stem cells (MSCs) transplantation may partially restore heart function in the treatment of acute myocardial infarction (AMI). The aim of this study was to explore the beneficial effects of MSCs modified with heme xygenase-1 (HO-1) on post-infarct swine hearts to determine whether the induction of therapeutic angiogenesis is modified by the angiogenic cytokines released from the implanted cells.Methods In vitro, MSCs were divided into four groups: (1) non-transfected MSCs (MSCs group), (2) MSCs transfected with the pcDNA3.1-Lacz plasmid (Lacz-MSCs group), (3) MSCs transfected with pcDNA3.1-hHO-1 (HO-1-MSCs group),and (4) MSCs transfected with pcDNA3.1-hHO-1 and pretreatment with an HO inhibitor, tin protoporphyrin (SnPP)(HO-1-MSCs+SnPP group). Cells were cultured in an airtight incubation bottle for 24 hours, in which the oxygen concentration was maintained at <1%, followed by 12 hours of reoxygenation. After hypoxia/reoxygen treatment, ELISA was used to measure transforming growth factor (TGF-β) and fibroblast growth factor (FGF-2) in the supernatant. In vivo,28 Chinese mini-pigs were randomly allocated to the following treatment groups: (1) control group (saline), (2)Lacz-MSCs group, (3) HO-1-MSCs group, and (4) HO-1-MSCs + SnPP group. About 1×107 of autologous stem cells or an idertical volume of saline was injected intracoronary into porcine hearts 1 hour after MI. Magnetic resonance imaging (MRI) assay and postmortem analysis were assessed four weeks after stem cell transplantation.Results Post hypoxia/reoxygenation in vitro, TGF-β in the supernatant was significantly increased in the HO-1-MSCs ((874.88±68.23) pg/ml) compared with Lacz-MSCs ((687.81±57.64) pg/ml, P <0.001). FGF-2 was also significantly increased in the HO-1-MSCs ((1106.48±107.06) pg/ml) compared with the Lacz-MSCs ((853.85±74.44) pg/ml, P <0.001 ).In vivo, at four weeks after transplantation, HO-1 gene transfer increased the capillary density in the peri-infarct area compared with the Lacz-MSCs group (14.24±1.66/HPFs vs. 11.51±1.34/HPFs, P <0.001). Arteriolar density was also significantly higher in HO-1-MSCs group than in the Lacz-MSCs group (7.86±2.00/HPFs vs. 6.45±1.74/HPFs, P=0.001).At the same time, the cardiac function was significantly improved in the HO-1-MSCs group compared with the Lacz-MSCs group ((53.17±3.55)% vs. (48.82±2.98)%, P <0.05). However, all these effects were significantly abrogated by SnPP.Conclusion MSCs provided a beneficial effect on cardiac function after ischemia/reperfusion by the induction of therapeutic angiogenesis, and this effect was amplified by HO-1 overexpression.

关键词

heme oxygenase-1 gene/mesenchymal stem cells/myocardial ischemia/reperfusion/vasculogenesis

Key words

heme oxygenase-1 gene/mesenchymal stem cells/myocardial ischemia/reperfusion/vasculogenesis

引用本文复制引用

JIANG Yi-bo,ZHANG Xiao-li,TANG Yao-liang,MA Gen-shan,SHEN Cheng-xing,WEI Qin,ZHU Qi,YAO Yu-yu,LIU Nai-feng..Effects of heme oxygenase-1 gene modulated mesenchymal stem cells on vasculogenesis in ischemic swine hearts[J].中华医学杂志(英文版),2011,124(3):401-407,7.

基金项目

This work was supported by a grant from National Basic Research Program in China (No. 30670853). (No. 30670853)

中华医学杂志(英文版)

OACSCDCSTPCDMEDLINESCI

0366-6999

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