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本文引用的文献

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Autologous stem cells in neurology: is there a future?神经科中的自体干细胞:是否有未来?
J Neural Transm (Vienna). 2013 Jan;120(1):65-73. doi: 10.1007/s00702-012-0913-9. Epub 2012 Nov 23.
2
CXCL12 enhances human neural progenitor cell survival through a CXCR7- and CXCR4-mediated endocytotic signaling pathway.CXCL12 通过 CXCR7 和 CXCR4 介导的内吞信号通路增强人神经祖细胞的存活。
Stem Cells. 2012 Nov;30(11):2571-83. doi: 10.1002/stem.1239.
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Visualizing dopamine transporter integrity with iodine-123-FP-CIT SPECT in combination with high resolution MRI in the brain of the common marmoset monkey.利用碘-123-FP-CIT SPECT 结合高分辨率 MRI 对普通猕猴大脑中的多巴胺转运体完整性进行可视化。
J Neurosci Methods. 2012 Sep 30;210(2):195-201. doi: 10.1016/j.jneumeth.2012.07.009. Epub 2012 Jul 22.
4
Bilateral transplantation of allogenic adult human bone marrow-derived mesenchymal stem cells into the subventricular zone of Parkinson's disease: a pilot clinical study.同种异体成人骨髓间充质干细胞经脑室下区移植入帕金森病患者:一项初步临床研究。
Stem Cells Int. 2012;2012:931902. doi: 10.1155/2012/931902. Epub 2012 Mar 13.
5
Long term behavioral effects of functional dopaminergic neurons generated from human neural stem cells in the rat 6-OH-DA Parkinson's disease model. Effects of the forced expression of BCL-X(L).人神经干细胞诱导分化的功能性多巴胺能神经元在大鼠 6-OH-DA 帕金森病模型中长期的行为学效应。BCL-X(L)强制表达的影响。
Behav Brain Res. 2012 Jun 15;232(1):225-32. doi: 10.1016/j.bbr.2012.04.020. Epub 2012 Apr 17.
6
The functional deficiency of bone marrow mesenchymal stromal cells in ALS patients is proportional to disease progression rate.肌萎缩侧索硬化症患者骨髓间充质基质细胞的功能缺陷与疾病进展速度成正比。
Exp Neurol. 2012 Jan;233(1):472-80. doi: 10.1016/j.expneurol.2011.11.021. Epub 2011 Nov 19.
7
The Movement Disorder Society Evidence-Based Medicine Review Update: Treatments for the motor symptoms of Parkinson's disease.运动障碍学会循证医学综述更新:帕金森病运动症状的治疗方法。
Mov Disord. 2011 Oct;26 Suppl 3:S2-41. doi: 10.1002/mds.23829.
8
Cell therapy in bone healing disorders.骨愈合障碍中的细胞疗法。
Orthop Rev (Pavia). 2010 Sep 23;2(2):e20. doi: 10.4081/or.2010.e20.
9
Epidemiology and etiology of Parkinson's disease: a review of the evidence.帕金森病的流行病学和病因学:证据回顾。
Eur J Epidemiol. 2011 Jun;26 Suppl 1:S1-58. doi: 10.1007/s10654-011-9581-6. Epub 2011 May 28.
10
Animal models of Parkinson's disease: a source of novel treatments and clues to the cause of the disease.帕金森病动物模型:新型治疗方法的来源和疾病病因的线索。
Br J Pharmacol. 2011 Oct;164(4):1357-91. doi: 10.1111/j.1476-5381.2011.01426.x.

基于细胞的帕金森病疗法。

Cell based therapy in Parkinsonism.

机构信息

Department of Neurosciences University Maastricht, Maastricht, The Netherlands.

出版信息

Transl Neurodegener. 2013 Jun 4;2(1):13. doi: 10.1186/2047-9158-2-13.

DOI:10.1186/2047-9158-2-13
PMID:23734727
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3674952/
Abstract

Parkinson's disease (PD) is a synucleinopathy-induced chronic progressive neurodegenerative disorder, worldwide affecting about 5 million humans. As of yet, actual therapies are symptomatic, and neuroprotective strategies are an unmet need. Due to their capability to transdifferentiate, to immune modulate and to increase neuroplasticity by producing neurotrophic factors, adult stem cells (ASC) might fill this gap. Preclinical research in 6-hydroxydopamine (6-OHDA) and/or 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) lesioned animals established persistent improvements of motor behavior after ASC-treatment. Histological/histochemical measurements in these animals evidenced an intracerebral applied ASC-induced increase of Tyrosine Hydroxylase-positive (TH+) cells with increased striatal dopamine levels, suggesting cell rescue. Likewise, clinical experience with subventricular applied ASCs in PD patients, although limited, is encouraging, evidencing neurorescue especially during the early phase of the disease. In multiple system atrophy (MSA) or progressive supranuclear palsy (PSP) patients, though, only marginal reduced progression of natural progression could be established after subventricular or intravasal ASC implantations.

摘要

帕金森病(PD)是一种由突触核蛋白病引起的慢性进行性神经退行性疾病,全球约有 500 万人受其影响。目前,实际的治疗方法是对症治疗,神经保护策略是未满足的需求。由于其具有转分化、免疫调节和产生神经营养因子增加神经可塑性的能力,成人干细胞(ASC)可能填补这一空白。在 6-羟基多巴胺(6-OHDA)和/或 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)损伤动物的临床前研究中,ASC 治疗后动物的运动行为持续改善。在这些动物中进行的组织学/组织化学测量表明,应用 ASC 可增加脑内酪氨酸羟化酶阳性(TH+)细胞,并增加纹状体多巴胺水平,提示细胞挽救。同样,在 PD 患者中,尽管应用于侧脑室的 ASC 的临床经验有限,但也令人鼓舞,表明神经挽救,特别是在疾病的早期阶段。然而,在多系统萎缩(MSA)或进行性核上性麻痹(PSP)患者中,仅能在侧脑室或血管内植入 ASC 后观察到自然进展的轻微减缓。