Adenovirus-mediated stromal cell-derived factor-1 alpha gene transfer improves cardiac structure and function after experimental myocardial infarction through angiogenic and antifibrotic actions.
Adenovirus-mediated stromal cell-derived factor-1 alpha gene transfer improves cardiac structure and function after experimental myocardial infarction through angiogenic and antifibrotic actions.
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腺病毒介导的基质细胞衍生因子 1 α 基因转移通过血管生成和抗纤维化作用改善实验性心肌梗死后的心脏结构和功能
DOI:
10.1007/s11033-009-9642-z
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发表时间:
2010-04
影响因子:
2.8
通讯作者:
Zhang L
中科院分区:
文献类型:
--
作者:
Tang J;Wang J;Song H;Huang Y;Yang J;Kong X;Guo L;Zheng F;Zhang L
Stromal cell-derived factor 1α (SDF-1) is not only a major chemotactic factor, but also an inducer of angiogenesis. The effects of SDF-1α on the left ventricular remodeling in a rat myocardial infarction (MI) model were analyzed. Myocardial infarction was induced by ligation of the left coronary artery in rats. 0.5 × 1010 pfu/ml AdV-SDF-1 or 0.5 × 1010 pfu/ml Adv-LacZ were immediately injected into the infarcted myocardium, 120 μl cell-free PBS were injected into the infarcted region or the myocardial wall in control, and sham group, respectively. We found that AdV-SDF-1 group had higher LVSP and ±dP/dtmax, lower LVEDP compared to control or Adv-LacZ group. The number of c-Kit+ stem cells, and gene expression of SDF-1, VEGF and bFGF were obviously increased, which was associated with reduced infarct size, thicker left ventricle wall, greater vascular density and cardiocytes density in infarcted hearts of AdV-SDF-1 group. Furthermore, the expression of collagen type I and type III mRNA, and collagen accumulation in the infarcted area was lower, which was associated with decreased TGF-β1, TIMP-1 and TIMP-2 expression in AdV-SDF-1 group. Conclusion: SDF-1α could improve cardiac structure and function after Myocardial infarction through angiogenic and anti-fibrotic actions. The online version of this article (doi:10.1007/s11033-009-9642-z) contains supplementary material, which is available to authorized users.
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影响因子:
9.5
作者:
Ma, J;Ge, JB;Zou, YZ
通讯作者:
Zou, YZ
影响因子:
2.2
作者:
Bloomston, M;Shafii, S;Rosemurgy, AS
通讯作者:
Rosemurgy, AS
影响因子:
37.8
作者:
Cimini, Massimo;Fazel, Shafie;Li, Ren-Ke
通讯作者:
Li, Ren-Ke
DOI:
10.1152/ajpheart.00370.2004
发表时间:
2005-01-01
影响因子:
4.8
作者:
Ikonomidis, JS;Hendrick, JW;Spinale, FG
通讯作者:
Spinale, FG
影响因子:
9.5
作者:
Koch, KC;Schaefer, WM;Weber, C
通讯作者:
Weber, C