Vazey Elena M, Aston-Jones Gary
J Clin Invest. 2014 Jul;124(7):2858-60. doi: 10.1172/JCI76833. Epub 2014 Jun 17.
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.
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。