Overexpression of Inducible Nitric Oxide Synthase Impairs the Survival of Bone marrow Stem Cells Transplanted into Rat Infarcted Myocardium

详细信息    查看全文

• 作者：Hong-min Li^a ; Lin Liu^a ; Xiang Mei^a ; Huajun Chen^b ; Zhenguo Liu^c ; Xue Zhao^a ; ^{xuezhao_cn@163.com" class="auth_mail}
• 关键词：Myocardial infarction ; Cell transplantation ; Bone marrow stem cell ; Nitric oxide ; Inducible nitric oxide synthase
• 刊名：Life Sciences
• 出版年：13 June 2014
• 年：2014
• 卷：106
• 期：1-2
• 页码：50-57
• 全文大小：1150 K

文摘

Inducible nitric oxide synthase (iNOS) over-expression is considered critical to the death of transplanted cells in infarcted myocardium. The present study was to investigate the effect of iNOS on the survival of transplanted bone marrow mesenchymal stem cells (BMSCs) in infarcted myocardium.

Main methods and key findings

Male rat BMSCs were injected into the infarct region of female rat hearts at 1 hour (H1, group A), day 3 (D3, group B), and day 7 (D7, group C) after coronary artery ligation, and harvested on D7 after transplantation. Myocardial iNOS expression was significantly increased shortly after coronary ligation with its peak on D3, and returned to baseline at D7. The cell survival rates were 6.2%, 2.1%, and 8.3% in group A, B, and C, respectively, one week after transplantation as assessed by detecting the Y-chromosome sry sequence in the infarct region. There was no significant difference in the survival rates between D7 and week 6 after cell transplantation in group A. Treating the animals in group B with the selective iNOS inhibitor 1400 W significantly increased the survival rate (from 1.8% to 4.2%). Apoptosis level of the transplanted cells was also significantly reduced with 1400 W treatment in group B.

Significance

BMSC transplantation on H1 and D7 after coronary ligation might be the optimal time for cell survival. The loss of transplanted BMSCs in the infarcted myocardium was partially due to increased apoptosis and iNOS overexpression. Selective iNOS inhibition early in myocardial infarction may increase the cell viability.