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In vivo induction of massive proliferation directed migration and differentiation of neural cells in the adult mammalian brain

机译:在体内诱导大量增殖 神经细胞的定向迁移和分化 成年哺乳动物的大脑

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摘要

The development of an in vivo procedure for the induction of massive proliferation, directed migration, and neurodifferentiation (PMD) in the damaged adult central nervous system would hold promise for the treatment of human neurodegenerative disorders such as Parkinson's disease. We investigated the in vivo induction of PMD in the forebrain of the adult rat by using a combination of 6-hydroxydopamine lesion of the substantia nigra dopaminergic neurons and infusions of transforming growth factor α (TGFα) into forebrain structures. Only in animals with both lesion and infusion of TGFα was there a rapid proliferation of forebrain stem cells followed by a timed migration of a ridge of neuronal and glial progenitors directed toward the region of the TGFα infusion site. Subsequently, increasing numbers of differentiated neurons were observed in the striatum. In behavioral experiments, there was a significant reduction of apomorphine-induced rotations in animals receiving the TGFα infusions. These results show that the brain contains stem cells capable of PMD in response to an exogenously administered growth factor. This finding has significant implications with respect to the development of treatments for both acute neural trauma and neurodegenerative diseases.
机译:在受损的成人中枢神经系统中诱导大量增殖,定向迁移和神经分化(PMD)的体内方法的发展将有望用于治疗人类神经退行性疾病,如帕金森氏病。我们通过使用黑质多巴胺能神经元的6-羟基多巴胺损伤和将转化生长因子α(TGFα)注入前脑结构的组合研究了成年大鼠前脑中PMD的体内诱导作用。仅在具有TGFα损伤和输注的动物中,前脑干细胞会快速增殖,随后神经元和神经胶质祖细胞的脊部会向TGFα输注部位区域定时迁移。随后,在纹状体中观察到越来越多的分化神经元。在行为实验中,接受TGFα输注的动物中阿扑吗啡引起的旋转明显减少。这些结果表明,大脑中含有能够响应外源性PMD的干细胞 管理的生长因子。这一发现具有重大意义 关于两种急性神经疾病的治疗方法的发展 创伤和神经退行性疾病。

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