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本文引用的文献

1
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J Clin Invest. 2014 Jul;124(7):3215-29. doi: 10.1172/JCI74664. Epub 2014 Jun 17.
2
Designer receptor manipulations reveal a role of the locus coeruleus noradrenergic system in isoflurane general anesthesia.设计受体操作揭示蓝斑去甲肾上腺素能系统在异氟醚全身麻醉中的作用。
Proc Natl Acad Sci U S A. 2014 Mar 11;111(10):3859-64. doi: 10.1073/pnas.1310025111. Epub 2014 Feb 24.
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Developing dopaminergic cell therapy for Parkinson's disease--give up or move forward?开发用于帕金森病的多巴胺能细胞治疗——放弃还是前进?
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New tricks for old dogmas: optogenetic and designer receptor insights for Parkinson's disease.旧教条的新花样:光遗传学和设计受体在帕金森病中的研究进展。
Brain Res. 2013 May 20;1511:153-63. doi: 10.1016/j.brainres.2013.01.021. Epub 2013 Jan 18.
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The emerging role of norepinephrine in cognitive dysfunctions of Parkinson's disease.去甲肾上腺素在帕金森病认知功能障碍中的新作用。
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The tumorigenicity of human embryonic and induced pluripotent stem cells.人胚胎干细胞和诱导多能干细胞的致瘤性。
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Neuropsychological and clinical heterogeneity of cognitive impairment and dementia in patients with Parkinson's disease.帕金森病患者认知障碍和痴呆的神经心理学和临床异质性。
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8
The A9 dopamine neuron component in grafts of ventral mesencephalon is an important determinant for recovery of motor function in a rat model of Parkinson's disease.移植腹侧中脑的 A9 多巴胺神经元成分是帕金森病大鼠模型运动功能恢复的重要决定因素。
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Remote control of neuronal activity in transgenic mice expressing evolved G protein-coupled receptors.对表达进化型G蛋白偶联受体的转基因小鼠神经元活动的远程控制。
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10
Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation.帕金森病患者移植神经元中的路易小体提示宿主到移植物的疾病传播。
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设计受体:帕金森病细胞替代疗法的治疗辅助手段

Designer receptors: therapeutic adjuncts to cell replacement therapy in Parkinson's disease.

作者信息

Vazey Elena M, Aston-Jones Gary

出版信息

J Clin Invest. 2014 Jul;124(7):2858-60. doi: 10.1172/JCI76833. Epub 2014 Jun 17.

DOI:10.1172/JCI76833
PMID:24937425
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4071398/
Abstract

Cell replacement for restoring neuronal populations in Parkinson's disease has been demonstrated as a potential therapeutic strategy over several decades of studies; however, a number of issues regarding sources of replacement neurons and optimization of therapeutic efficacy in vivo have hampered clinical implementation. In this issue of the JCI, Dell'Anno and colleagues evaluated the use of induced dopaminergic (iDA) neurons that were generated by direct fibroblast reprogramming for transplantation and demonstrated that postmitotic iDA neurons stably and functionally integrate into host striatum to produce motor improvements in 6-OHDA rats, a Parkinson's disease model. Furthermore, using designer receptors exclusively activated by designer drugs (DREADDs) in iDA grafts to noninvasively increase dopamine release from grafted neurons, the authors were able to remotely control transplanted neurons and enhance therapeutic efficacy. This initial proof-of-concept study is the first application of DREADD technology to treat neurodegenerative dysfunction, and by using DREADDs as an adjunct to iDA cell therapy, it presents a novel strategy to overcome some current caveats of cell replacement therapy.

摘要

几十年来的研究表明,细胞替代疗法可用于恢复帕金森病患者的神经元数量,是一种潜在的治疗策略;然而,关于替代神经元的来源以及体内治疗效果优化等诸多问题阻碍了其临床应用。在本期《临床研究杂志》中,戴尔·安诺及其同事评估了通过直接重编程成纤维细胞生成的诱导多巴胺能(iDA)神经元用于移植的情况,并证明有丝分裂后的iDA神经元能稳定且功能性地整合到宿主纹状体中,从而使帕金森病模型6-羟基多巴胺(6-OHDA)大鼠的运动功能得到改善。此外,作者通过在iDA移植物中使用仅由设计药物激活的设计受体(DREADDs)来无创增加移植神经元释放多巴胺,从而能够远程控制移植神经元并提高治疗效果。这项初步的概念验证研究是DREADD技术首次应用于治疗神经退行性疾病功能障碍,并且通过将DREADDs作为iDA细胞疗法的辅助手段,它提出了一种克服当前细胞替代疗法一些缺陷的新策略。