Fallon J, Reid S, Kinyamu R, Opole I, Opole R, Baratta J, Korc M, Endo T L, Duong A, Nguyen G, Karkehabadhi M, Twardzik D, Patel S, Loughlin S
Departments of Anatomy and Neurobiology, Medicine, and Pharmacology, University of California, Irvine, CA 92697-1275, USA.
Proc Natl Acad Sci U S A. 2000 Dec 19;97(26):14686-91. doi: 10.1073/pnas.97.26.14686.
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 alpha (TGFalpha) into forebrain structures. Only in animals with both lesion and infusion of TGFalpha 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 TGFalpha 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 TGFalpha 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.
开发一种能在受损成年中枢神经系统中诱导大量增殖、定向迁移和神经分化(PMD)的体内程序,有望用于治疗人类神经退行性疾病,如帕金森病。我们通过将黑质多巴胺能神经元的6-羟基多巴胺损伤与向脑前结构中注入转化生长因子α(TGFα)相结合,研究了成年大鼠前脑PMD的体内诱导情况。只有在同时有损伤和注入TGFα的动物中,前脑干细胞才会迅速增殖,随后一群神经元和神经胶质祖细胞会定时迁移至TGFα注入部位区域。随后,在纹状体中观察到分化神经元数量增加。在行为实验中,接受TGFα注入的动物中,阿扑吗啡诱导的旋转显著减少。这些结果表明,大脑中含有能够对外源性给予的生长因子产生PMD反应的干细胞。这一发现对于急性神经创伤和神经退行性疾病治疗方法的开发具有重要意义。