成人体内多巴胺能系统中Rheb/mTORC1信号通路的神经保护机制

K. H. Jeong, Sang Ryong Kim
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摘要

尽管进行了大量的研究,但尚未开发出有效的帕金森病药物治疗方法。然而,随着高效基因传递系统的发展,PD的基因治疗已成为研究热点,越来越多的证据表明,神经营养因子的持续产生在黑质纹状体多巴胺能(DA)系统的功能恢复中起着重要作用。我们最近报道了病毒载体介导的hRheb(S16H)表达可在体内诱导成年DA神经元中胶质细胞系源性神经营养因子(GDNF)和脑源性神经营养因子(BDNF)的表达。此外,我们发现hRheb(S16H)诱导的神经营养因子表达依赖于mTORC1活性和受保护的黑质纹状体DA投射。我们的观察结果表明,hRheb(S16H)在成熟DA神经元中的表达促进了多种神经营养因子(如GDNF和BDNF)的产生,并且多种因素参与了成人大脑黑质纹状体DA系统的维持和保护。在本研究重点中,我们简要概述了我们最近发表的研究结果,这些发现证明了hRheb(S16H)对体内黑质纹状体DA投射的神经保护机制。
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Neuroprotective mechanisms of the Rheb/mTORC1 signaling pathway in the adult dopaminergic system in vivo
Despite intensive research effort, no effective pharmacological therapies for Parkinson’s disease (PD) have been developed. However, with the development of efficient gene delivery systems, gene therapy for PD has become a focus of research, and increasing evidences suggest that continuous production of neurotrophic factors plays a significant role in the functional restoration of the nigrostriatal dopaminergic (DA) system. We recently reported that viral vector-mediated hRheb(S16H) expression robustly induced glial cell line-derived neurotrophic factor (GDNF) and brain-derived neurotrophic factor (BDNF) expression in adult DA neurons in vivo . Furthermore, we showed that hRheb(S16H)-induced neurotrophic factor expression was dependent on mTORC1 activity and protected nigrostriatal DA projections. Our observations suggest that hRheb(S16H) expression in mature DA neurons facilitates the production of diverse neurotrophic factors such as GDNF and BDNF, and that multiple factors are involved in the maintenance and protection of the nigrostriatal DA system in the adult brain. In this research highlight, we provide a brief overview of our most recent published findings, which demonstrate the neuroprotective mechanisms of hRheb(S16H) on nigrostriatal DA projections in vivo .
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