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比较脑卒中大鼠和正常大鼠骨髓基质细胞在脑卒中治疗中的应用。

Comparison of bone marrow stromal cells derived from stroke and normal rats for stroke treatment.

机构信息

Department of Neurology, Henry Ford Health Sciences Center, Detroit, Mich 48202, USA.

出版信息

Stroke. 2010 Mar;41(3):524-30. doi: 10.1161/STROKEAHA.109.568881. Epub 2010 Jan 7.

Abstract

BACKGROUND AND PURPOSE

We compared the effect of treatment of stroke with bone marrow stromal cells from stroke rats (Isch-BMSC) and normal rats (Nor-BMSC) on functional outcome.

METHODS

Isch-BMSCs and Nor-BMSCs were intravenously injected into rats 24 hours after middle cerebral artery occlusion. To test the mechanism of Isch-BMSC-enhanced neurorestoration, Isch-BMSC and Nor-BMSC cultures were used.

RESULTS

Isch-BMSC significantly promoted functional outcome and enhanced angiogenesis, arterial density, and axonal regeneration compared with Nor-BMSC treatment animals. Isch-BMSCs exhibited increased Angiopoietin-1, Tie2, basic fibroblast growth factor, glial cell-derived neurotrophic factor, vascular endothelial growth factor, and Flk1 gene expression compared with Nor-BMSC. Using transwell coculture of BMSCs with brain-derived endothelial cells, Isch-BMSCs increased phosphorylated-Tie2 activity in brain-derived endothelial cells and enhanced brain-derived endothelial cells capillary tube formation compared with Nor-BMSCs. Inhibition of Tie2 gene expression in brain-derived endothelial cells using siRNA significantly attenuated BMSC-induced capillary tube formation.

CONCLUSIONS

These data suggest that Isch-BMSCs are superior to Nor-BMSCs for the neurorestorative treatment of stroke, which may be mediated by the enhanced trophic factor and angiogenic characteristics of Isch-BMSCs.

摘要

背景与目的

我们比较了骨髓基质细胞(BMSCs)治疗缺血性脑卒中大鼠(Isch-BMSC)和正常大鼠(Nor-BMSC)的效果,以评估其对功能恢复的影响。

方法

在大脑中动脉闭塞后 24 小时,将 Isch-BMSCs 和 Nor-BMSCs 静脉注射到大鼠体内。为了研究 Isch-BMSC 增强神经修复的机制,我们进行了 Isch-BMSC 和 Nor-BMSC 的培养实验。

结果

与 Nor-BMSC 治疗组相比,Isch-BMSC 显著促进了功能恢复,增强了血管生成、动脉密度和轴突再生。与 Nor-BMSC 相比,Isch-BMSCs 表现出更高的血管生成素-1、Tie2、碱性成纤维细胞生长因子、胶质细胞源性神经营养因子、血管内皮生长因子和 Flk1 基因表达水平。通过 BMSCs 与脑源性内皮细胞的 Transwell 共培养实验,我们发现 Isch-BMSCs 能够增加脑源性内皮细胞中磷酸化-Tie2 的活性,并增强脑源性内皮细胞的毛细血管管腔形成。使用 siRNA 抑制脑源性内皮细胞中的 Tie2 基因表达,显著减弱了 BMSC 诱导的毛细血管管腔形成。

结论

这些数据表明,Isch-BMSCs 比 Nor-BMSC 更适合缺血性脑卒中的神经修复治疗,这可能是由 Isch-BMSCs 增强的营养因子和血管生成特性介导的。

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