Honma T, Honmou O, Iihoshi S, Harada K, Houkin K, Hamada H, Kocsis J D
Department of Neurosurgery, Sapporo Medical University School of Medicine, South-1st, West-16th, Chuo-ku, Sapporo, Hokkaido 060-8543, Japan.
Exp Neurol. 2006 May;199(1):56-66. doi: 10.1016/j.expneurol.2005.05.004. Epub 2005 Jun 20.
Intravenous infusion of bone marrow cells has demonstrated therapeutic efficacy in animal models of cerebral ischemia and spinal cord injury. We intravenously delivered human mesenchymal stem cells (SH2+, SH3+, CD34-, and CD45-) immortalized with a human-telomerase gene (hTERT-MSCs) and transfected with eGFP or LacZ into rats 12 h after induction of transient middle cerebral artery occlusion (MCAO), to study their potential therapeutic benefit. hTERT-MSCs were delivered at 12 h after lesion induction. Lesion size was assessed using MR imaging and spectroscopy, and histological methods. Functional outcome was assessed using the Morris water maze and a treadmill test. Intravenous delivery of hTERT-MSCs reduced lesion volume and the magnitude of the reduction and functional improvement was positively correlated with the number of cells injected. The reduction of lesion size could be assessed in vivo with MRI and MRS and was correlated with subsequent histological examination of the brain. This work demonstrates that highly purified hTERT-MSCs reduce cerebral infarction volume and improve functional outcome.
静脉输注骨髓细胞已在脑缺血和脊髓损伤的动物模型中显示出治疗效果。我们在短暂性大脑中动脉闭塞(MCAO)诱导后12小时,将用人端粒酶基因永生化(SH2 +、SH3 +、CD34 -和CD45 -)并转染了eGFP或LacZ的人间充质干细胞(hTERT-MSCs)静脉注射到大鼠体内,以研究其潜在的治疗益处。hTERT-MSCs在损伤诱导后12小时给药。使用磁共振成像和波谱以及组织学方法评估损伤大小。使用莫里斯水迷宫和跑步机试验评估功能结局。静脉注射hTERT-MSCs可减少损伤体积,减少的幅度与功能改善与注射的细胞数量呈正相关。损伤大小的减少可以通过MRI和MRS在体内进行评估,并且与随后的脑组织学检查相关。这项工作表明,高度纯化的hTERT-MSCs可减少脑梗死体积并改善功能结局。