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本文引用的文献

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How to optimize the treatment of early stage Parkinson's disease.如何优化早期帕金森病的治疗。
Transl Neurodegener. 2015 Feb 25;4:4. doi: 10.1186/2047-9158-4-4. eCollection 2015.
2
Treatment of the later stages of Parkinson's disease - pharmacological approaches now and in the future.帕金森病晚期的治疗——现在及未来的药物治疗方法。
Transl Neurodegener. 2015 Feb 12;4:3. doi: 10.1186/2047-9158-4-3. eCollection 2015.
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Mitochondrial alterations by PARKIN in dopaminergic neurons using PARK2 patient-specific and PARK2 knockout isogenic iPSC lines.帕金森病基因 PARKIN 导致多巴胺能神经元中线粒体改变:使用 PARK2 患者特异性和 PARK2 基因敲除同基因诱导多能干细胞系。
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Neural stem cells could serve as a therapeutic material for age-related neurodegenerative diseases.神经干细胞可以作为一种治疗与年龄相关的神经退行性疾病的治疗材料。
World J Stem Cells. 2015 Mar 26;7(2):502-11. doi: 10.4252/wjsc.v7.i2.502.
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Successful function of autologous iPSC-derived dopamine neurons following transplantation in a non-human primate model of Parkinson's disease.在帕金森病非人灵长类动物模型中移植后,自体诱导多能干细胞衍生的多巴胺神经元功能成功实现。
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Parkinson's disease: animal models and dopaminergic cell vulnerability.帕金森病:动物模型与多巴胺能细胞易损性
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Therapeutic strategies in Parkinson's disease: what we have learned from animal models.帕金森病的治疗策略:我们从动物模型中学到了什么。
Ann N Y Acad Sci. 2015 Mar;1338:16-37. doi: 10.1111/nyas.12577. Epub 2014 Dec 16.
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Reprint of "iPSCs, aging and age-related diseases".《诱导多能干细胞、衰老与年龄相关疾病》重印版
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iPSC-derived dopamine neurons reveal differences between monozygotic twins discordant for Parkinson's disease.诱导多能干细胞衍生的多巴胺神经元揭示了患帕金森病的同卵双胞胎之间的差异。
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Parkin mutations reduce the complexity of neuronal processes in iPSC-derived human neurons.帕金森病基因(Parkin)突变降低了诱导多能干细胞(iPSC)衍生的人类神经元中神经突的复杂性。
Stem Cells. 2015 Jan;33(1):68-78. doi: 10.1002/stem.1854.

诱导多能干细胞与帕金森病:建模与治疗

Induced pluripotent stem cells and Parkinson's disease: modelling and treatment.

作者信息

Xu Xiaoyun, Huang Jinsha, Li Jie, Liu Ling, Han Chao, Shen Yan, Zhang Guoxin, Jiang Haiyang, Lin Zhicheng, Xiong Nian, Wang Tao

机构信息

Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

Department of Psychiatry, Harvard Medical School, Division of Alcohol and Drug Abuse, Mailman Neuroscience Research Center, McLean Hospital, Belmont, MA, USA.

出版信息

Cell Prolif. 2016 Feb;49(1):14-26. doi: 10.1111/cpr.12229. Epub 2016 Jan 8.

DOI:10.1111/cpr.12229
PMID:26748765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6495331/
Abstract

Many neurodegenerative disorders, such as Parkinson's disease (PD), are characterized by progressive neuronal loss in different regions of the central nervous system, contributing to brain dysfunction in the relevant patients. Stem cell therapy holds great promise for PD patients, including with foetal ventral mesencephalic cells, human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs). Moreover, stem cells can be used to model neurodegenerative diseases in order to screen potential medication and explore their mechanisms of disease. However, related ethical issues, immunological rejection and lack of canonical grafting protocols limit common clinical use of stem cells. iPSCs, derived from reprogrammed somatic cells, provide new hope for cell replacement therapy. In this review, recent development in stem cell treatment for PD, using hiPSCs, as well as the potential value of hiPSCs in modelling for PD, have been summarized for application of iPSCs technology to clinical translation for PD treatment.

摘要

许多神经退行性疾病,如帕金森病(PD),其特征是中枢神经系统不同区域的神经元进行性丧失,导致相关患者出现脑功能障碍。干细胞疗法对PD患者具有巨大潜力,包括使用胎儿腹侧中脑细胞、人类胚胎干细胞(hESC)和人类诱导多能干细胞(hiPSC)。此外,干细胞可用于模拟神经退行性疾病,以筛选潜在药物并探索其发病机制。然而,相关的伦理问题、免疫排斥以及缺乏规范的移植方案限制了干细胞在临床上的普遍应用。由重编程体细胞衍生而来的hiPSC为细胞替代疗法带来了新希望。在本综述中,总结了使用hiPSC进行PD干细胞治疗的最新进展,以及hiPSC在PD建模中的潜在价值,以便将iPSC技术应用于PD治疗的临床转化。