Department of Neurology, Henry Ford Health Sciences Center, Detroit, Mich 48202, USA.
Stroke. 2010 Mar;41(3):524-30. doi: 10.1161/STROKEAHA.109.568881. Epub 2010 Jan 7.
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.
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.
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.
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.
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。
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。
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。
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。