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

被引:311
作者
Fallon, J [1 ]
Reid, S
Kinyamu, R
Opole, I
Opole, R
Baratta, J
Korc, M
Endo, TL
Duong, A
Nguyen, G
Karkehabadhi, M
Twardzik, D
Loughlin, S
机构
[1] Univ Calif Irvine, Dept Anat & Neurobiol, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Med, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Pharmacol, Irvine, CA 92697 USA
[4] Stem Cell Pharmaceut, Seattle, WA 98104 USA
关键词
D O I
10.1073/pnas.97.26.14686
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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 alpha (TGF alpha) into forebrain structures. Only in animals with both lesion and infusion of TGF alpha 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 TGF alpha 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 TGF alpha 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.
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页码:14686 / 14691
页数:6
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