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本文引用的文献

1
Progress and prospects: stem cells and neurological diseases.进展与展望:干细胞与神经退行性疾病
Gene Ther. 2011 Jan;18(1):1-6. doi: 10.1038/gt.2010.130. Epub 2010 Sep 30.
2
SDF-1α secreted by human CD133-derived multipotent stromal cells promotes neural progenitor cell survival through CXCR7.人源 CD133 源性多能基质细胞分泌的 SDF-1α 通过 CXCR7 促进神经祖细胞存活。
Stem Cells Dev. 2011 Jun;20(6):1021-9. doi: 10.1089/scd.2010.0198. Epub 2010 Nov 9.
3
Human CD133-derived bone marrow stromal cells establish ectopic hematopoietic microenvironments in immunodeficient mice.人源 CD133 阳性骨髓基质细胞在免疫缺陷小鼠体内构建异位造血微环境。
Biochem Biophys Res Commun. 2010 Sep 17;400(2):212-8. doi: 10.1016/j.bbrc.2010.08.040. Epub 2010 Aug 16.
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Epigenetic memory in induced pluripotent stem cells.诱导多能干细胞中的表观遗传记忆。
Nature. 2010 Sep 16;467(7313):285-90. doi: 10.1038/nature09342.
5
Therapeutic potential of appropriately evaluated safe-induced pluripotent stem cells for spinal cord injury.安全评估诱导多能干细胞治疗脊髓损伤的潜力。
Proc Natl Acad Sci U S A. 2010 Jul 13;107(28):12704-9. doi: 10.1073/pnas.0910106107. Epub 2010 Jul 6.
6
A long-term follow-up study of intravenous autologous mesenchymal stem cell transplantation in patients with ischemic stroke.静脉内自体间充质干细胞移植治疗缺血性脑卒中的长期随访研究。
Stem Cells. 2010 Jun;28(6):1099-106. doi: 10.1002/stem.430.
7
Comparison of contractile behavior of native murine ventricular tissue and cardiomyocytes derived from embryonic or induced pluripotent stem cells.比较天然鼠心室组织和源自胚胎或诱导多能干细胞的心肌细胞的收缩行为。
FASEB J. 2010 Aug;24(8):2739-51. doi: 10.1096/fj.09-145177. Epub 2010 Apr 6.
8
Factors Released from Embryonic Stem Cells Stimulate c-kit-FLK-1(+ve) Progenitor Cells and Enhance Neovascularization.胚胎干细胞释放的因子刺激 c-kit-FLK-1(+ve) 祖细胞并增强血管生成。
Antioxid Redox Signal. 2010 Dec 15;13(12):1857-65. doi: 10.1089/ars.2010.3104. Epub 2010 Jul 28.
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Direct reprogramming 101.直接重编程 101。
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10
Tridermal tumorigenesis of induced pluripotent stem cells transplanted in ischemic brain.诱导多能干细胞移植治疗缺血性脑后形成的三表皮肿瘤。
J Cereb Blood Flow Metab. 2010 Aug;30(8):1487-93. doi: 10.1038/jcbfm.2010.32. Epub 2010 Mar 10.

神经修复用干细胞和祖细胞:旁分泌治疗的次要问题、主要障碍和令人兴奋的机会。

Stem and progenitor cells for neurological repair: minor issues, major hurdles, and exciting opportunities for paracrine-based therapeutics.

机构信息

Department of Medicine, Stem Cell Core, University of Vermont, Colchester, Vermont 05446, USA.

出版信息

J Cell Biochem. 2011 Feb;112(2):374-80. doi: 10.1002/jcb.22963.

DOI:10.1002/jcb.22963
PMID:21268056
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3175770/
Abstract

The transplantation of cultured stem and progenitor cells is a key element in the rapidly growing field of regenerative medicine. Based on their ability to rescue and/or repair injured tissue and partially restore organ function, multiple types of stem/progenitor cells have already entered into clinical trials. However, despite several decades of intense research, the goal to apply culture-expanded stem/progenitor cells in a manner that can effectively replace cells after injury has yet to be realized. Many sources of potentially useful cells are available, but something is clearly missing. In addition, recent studies suggest that paracrine effects of secreted or released factors are responsible for most of the benefits observed after cell transplantation, rather than direct cell replacement. These data call into question the need for cell transplantation for many types of therapy, in particular for acute injuries such as myocardial infarction and stroke. In this review, we examine current progress in the area of cell transplantation and minor issues and major hurdles regarding the clinical application of different cell types. We discuss the "paracrine hypothesis" for the action of transplanted stem/progenitor cells as an opportunity to identify defined combinations of biomolecules to rescue and/or repair tissues after injury. Although many of the concepts in this review will apply to multiple injury/repair systems, we will focus primarily on stem/progenitor cell-based treatments for neurological disorders and stroke.

摘要

培养的干细胞和祖细胞移植是再生医学这一快速发展领域的关键要素。基于其拯救和/或修复受损组织并部分恢复器官功能的能力,多种类型的干细胞/祖细胞已经进入临床试验。然而,尽管经过了几十年的深入研究,将培养扩增的干细胞/祖细胞应用于有效替代损伤后细胞的目标尚未实现。有许多潜在有用的细胞来源,但显然缺少了某些东西。此外,最近的研究表明,分泌或释放的因子的旁分泌作用是细胞移植后观察到的大多数益处的原因,而不是直接的细胞替代。这些数据对许多类型的治疗(特别是心肌梗死和中风等急性损伤)是否需要细胞移植提出了质疑。在这篇综述中,我们检查了细胞移植领域的当前进展,以及不同细胞类型临床应用中的次要问题和主要障碍。我们讨论了移植的干细胞/祖细胞作用的“旁分泌假说”,将其作为确定生物分子组合以在损伤后拯救和/或修复组织的机会。尽管本综述中的许多概念将适用于多种损伤/修复系统,但我们将主要关注基于干细胞/祖细胞的神经疾病和中风治疗。