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本文引用的文献

1
TNF-α respecifies human mesenchymal stem cells to a neural fate and promotes migration toward experimental glioma.TNF-α 将人骨髓间充质干细胞重编程为神经命运细胞,并促进其向实验性神经胶质瘤迁移。
Cell Death Differ. 2011 May;18(5):853-63. doi: 10.1038/cdd.2010.154. Epub 2010 Dec 3.
2
Migration of engrafted neural stem cells is mediated by CXCL12 signaling through CXCR4 in a viral model of multiple sclerosis.移植的神经干细胞通过 CXCR4 介导的 CXCL12 信号迁移在多发性硬化的病毒模型中。
Proc Natl Acad Sci U S A. 2010 Jun 15;107(24):11068-73. doi: 10.1073/pnas.1006375107. Epub 2010 Jun 1.
3
Human stem cells expressing novel TSP-1 variant have anti-angiogenic effect on brain tumors.表达新型 TSP-1 变体的人干细胞对脑肿瘤具有抗血管生成作用。
Oncogene. 2010 Jun 3;29(22):3185-95. doi: 10.1038/onc.2010.75. Epub 2010 Mar 22.
4
HGF upregulates CXCR4 expression in gliomas via NF-kappaB: implications for glioma cell migration.HGF 通过 NF-κB 上调神经胶质瘤中 CXCR4 的表达:对神经胶质瘤细胞迁移的影响。
J Neurooncol. 2010 Aug;99(1):33-40. doi: 10.1007/s11060-010-0111-2. Epub 2010 Feb 16.
5
A novel molecule integrating therapeutic and diagnostic activities reveals multiple aspects of stem cell-based therapy.一种新型分子集治疗和诊断活动于一体,揭示了基于干细胞治疗的多个方面。
Stem Cells. 2010 Apr;28(4):832-41. doi: 10.1002/stem.313.
6
Neural stem cells as a novel platform for tumor-specific delivery of therapeutic antibodies.神经干细胞作为治疗性抗体肿瘤特异性递呈的新平台。
PLoS One. 2009 Dec 15;4(12):e8314. doi: 10.1371/journal.pone.0008314.
7
Transplantation of human neural stem cells transduced with Olig2 transcription factor improves locomotor recovery and enhances myelination in the white matter of rat spinal cord following contusive injury.用Olig2转录因子转导的人神经干细胞移植可改善大鼠脊髓挫伤后运动功能恢复并增强白质髓鞘形成。
BMC Neurosci. 2009 Sep 22;10:117. doi: 10.1186/1471-2202-10-117.
8
Targeting rat brainstem glioma using human neural stem cells and human mesenchymal stem cells.利用人神经干细胞和人间充质干细胞靶向治疗大鼠脑干胶质瘤。
Clin Cancer Res. 2009 Aug 1;15(15):4925-34. doi: 10.1158/1078-0432.CCR-08-3076. Epub 2009 Jul 28.
9
Matrix metalloproteinase-9 is essential for ischemia-induced neovascularization by modulating bone marrow-derived endothelial progenitor cells.基质金属蛋白酶-9通过调节骨髓来源的内皮祖细胞对缺血诱导的新生血管形成至关重要。
Arterioscler Thromb Vasc Biol. 2009 Aug;29(8):1179-84. doi: 10.1161/ATVBAHA.109.189175. Epub 2009 May 21.
10
Molecular and magnetic resonance imaging of human embryonic stem cell-derived neural stem cell grafts in ischemic rat brain.人胚胎干细胞源性神经干细胞移植入缺血大鼠脑内的分子与磁共振成像
Mol Ther. 2009 Jul;17(7):1282-91. doi: 10.1038/mt.2009.104. Epub 2009 May 12.

治疗性干细胞在不同脑疾病模型中的迁移和命运。

Migration and fate of therapeutic stem cells in different brain disease models.

机构信息

Molecular Neurotherapy and Imaging Laboratory, Department of Radiology and Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Neuroscience. 2011 Dec 1;197:37-47. doi: 10.1016/j.neuroscience.2011.08.063. Epub 2011 Sep 14.

DOI:10.1016/j.neuroscience.2011.08.063
PMID:21946010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3589128/
Abstract

Stem cells have a number of properties, which make them excellent candidates for the treatment of various neurologic disorders, the most important of which being their ability to migrate to and differentiate predictably at sites of pathology in the brain. The disease-directed migration and well-characterized differentiation patterns of stem cells may eventually provide a powerful tool for the treatment of both localized and diffuse disease processes within the human brain. A thorough understanding of the molecular mechanisms governing their migratory properties and their choice between different differentiation programs is essential if these cells are to be used therapeutically in humans. This review focuses on summarizing the migration and differentiation of therapeutic neural and mesenchymal stem cells in different disease models in the brain and also discusses the promise of these cells to eventually treat various forms of neurologic disease.

摘要

干细胞具有多种特性,使其成为治疗各种神经疾病的理想候选者,其中最重要的特性是它们能够迁移到大脑病变部位并可预测地分化。干细胞的疾病定向迁移和特征明确的分化模式最终可能为治疗人脑内局部和弥漫性疾病提供强有力的工具。如果要在人类中对这些细胞进行治疗,就必须深入了解控制其迁移特性的分子机制及其在不同分化程序之间的选择。本综述重点总结了治疗性神经和间充质干细胞在大脑不同疾病模型中的迁移和分化,并讨论了这些细胞最终治疗各种形式的神经疾病的前景。