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Intravenous infusion of immortalized human mesenchymal stem cells protects against injury in a cerebral ischemia model in adult rat.静脉输注永生化人骨髓间充质干细胞可保护成年大鼠脑缺血模型免受损伤。
Exp Neurol. 2006 May;199(1):56-66. doi: 10.1016/j.expneurol.2005.05.004. Epub 2005 Jun 20.
2
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Macrophage Subpopulation Dynamics Shift following Intravenous Infusion of Mesenchymal Stromal Cells.静脉输注间充质基质细胞后巨噬细胞亚群动力学变化。
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本文引用的文献

1
Mesenchymal stem cells that produce neurotrophic factors reduce ischemic damage in the rat middle cerebral artery occlusion model.产生神经营养因子的间充质干细胞可减轻大鼠大脑中动脉闭塞模型中的缺血性损伤。
Mol Ther. 2005 Jan;11(1):96-104. doi: 10.1016/j.ymthe.2004.09.020.
2
A therapeutic window for intravenous administration of autologous bone marrow after cerebral ischemia in adult rats.成年大鼠脑缺血后自体骨髓静脉注射的治疗窗。
Brain Res. 2004 May 8;1007(1-2):1-9. doi: 10.1016/j.brainres.2003.09.084.
3
BDNF gene-modified mesenchymal stem cells promote functional recovery and reduce infarct size in the rat middle cerebral artery occlusion model.脑源性神经营养因子基因修饰的间充质干细胞促进大鼠大脑中动脉闭塞模型的功能恢复并减小梗死面积。
Mol Ther. 2004 Feb;9(2):189-97. doi: 10.1016/j.ymthe.2003.10.012.
4
Fusion of bone-marrow-derived cells with Purkinje neurons, cardiomyocytes and hepatocytes.骨髓来源的细胞与浦肯野神经元、心肌细胞和肝细胞的融合。
Nature. 2003 Oct 30;425(6961):968-73. doi: 10.1038/nature02069. Epub 2003 Oct 12.
5
Comparative analysis of remyelinating potential of focal and intravenous administration of autologous bone marrow cells into the rat demyelinated spinal cord.大鼠脱髓鞘脊髓局部和静脉注射自体骨髓细胞后再髓鞘化潜力的比较分析
Glia. 2003 Nov;44(2):111-8. doi: 10.1002/glia.10285.
6
Telomerized human multipotent mesenchymal cells can differentiate into hematopoietic and cobblestone area-supporting cells.端粒化的人多能间充质细胞可分化为造血细胞和鹅卵石区域支持细胞。
Exp Hematol. 2003 Aug;31(8):715-22. doi: 10.1016/s0301-472x(03)00177-2.
7
Delayed transplantation of olfactory ensheathing glia promotes sparing/regeneration of supraspinal axons in the contused adult rat spinal cord.嗅鞘胶质细胞的延迟移植促进成年大鼠脊髓挫伤后脊髓上轴突的保留/再生。
J Neurotrauma. 2003 Jan;20(1):1-16. doi: 10.1089/08977150360517146.
8
Ischemic rat brain extracts induce human marrow stromal cell growth factor production.缺血大鼠脑提取物诱导人骨髓基质细胞生长因子的产生。
Neuropathology. 2002 Dec;22(4):275-9. doi: 10.1046/j.1440-1789.2002.00450.x.
9
Expansion of human adult stem cells from bone marrow stroma: conditions that maximize the yields of early progenitors and evaluate their quality.从骨髓基质中扩增人类成体干细胞:使早期祖细胞产量最大化并评估其质量的条件。
Stem Cells. 2002;20(6):530-41. doi: 10.1634/stemcells.20-6-530.
10
Ex vivo expansion of human umbilical cord hematopoietic progenitor cells using a coculture system with human telomerase catalytic subunit (hTERT)-transfected human stromal cells.使用与人端粒酶催化亚基(hTERT)转染的人基质细胞共培养系统对人脐带造血祖细胞进行体外扩增。
Blood. 2003 Jan 15;101(2):532-40. doi: 10.1182/blood-2002-04-1268. Epub 2002 Sep 5.

静脉输注永生化人骨髓间充质干细胞可保护成年大鼠脑缺血模型免受损伤。

Intravenous infusion of immortalized human mesenchymal stem cells protects against injury in a cerebral ischemia model in adult rat.

作者信息

Honma T, Honmou O, Iihoshi S, Harada K, Houkin K, Hamada H, Kocsis J D

机构信息

Department of Neurosurgery, Sapporo Medical University School of Medicine, South-1st, West-16th, Chuo-ku, Sapporo, Hokkaido 060-8543, Japan.

出版信息

Exp Neurol. 2006 May;199(1):56-66. doi: 10.1016/j.expneurol.2005.05.004. Epub 2005 Jun 20.

DOI:10.1016/j.expneurol.2005.05.004
PMID:15967439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2605388/
Abstract

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.

摘要

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。