Neural stem cells in development and regenerative medicine

被引:27
作者
Baizabal, JM [1 ]
Furlan-Magaril, M [1 ]
Santa-Olalla, J [1 ]
Covarrubias, L [1 ]
机构
[1] Univ Nacl Autonoma Mexico, IBT, Dept Genet Desarrollo & Fisiol Mol, Cuernavaca 62250, Morelos, Mexico
关键词
neurogenesis; neural precursor cells; differentiation; neurosphere; transplantation;
D O I
10.1016/j.arcmed.2003.09.002
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
In the last 10 years, enormous interest in neural stem cells has arisen from both basic and medical points of view. The discovery of neurogenesis in the adult brain has opened our imagination to consider novel strategies for the treatment of neurodegenerative diseases. Characterization of neurogenesis during development plays a fundamental role for the rational design of therapeutic procedures. In the present review, we describe recent progress in the characterization of embryo and adult neural stem cells (NSCs). We emphasize studies directed to determine the in vivo and in vitro differentiation potential of different NSC populations and the influence of the surrounding environment on NSC-specific differentiation. From a different perspective, the fact that NSCs and progenitors continuously proliferate and differentiate in some areas of the adult brain force us to ask how this process can be affected in neurodegenerative diseases. We propose that both abnormal cell death activation and decreased natural neuronal regeneration can contribute to the neuronal loss associated with aging, and perhaps even with that occurring in some neurodegenerative diseases. Furthermore, although NSC activation can be useful to treat neurodegenerative diseases, uncontrolled NSC proliferation, survival, and/or differentiation could cause tumorigenesis in the brain. NSC-mediated therapeutic procedures must take into account this latter possibility. (C) 2004 IMSS. Published by Elsevier Inc.
引用
收藏
页码:572 / 588
页数:17
相关论文
共 162 条
[11]   Apoptosis and proliferation of dentate gyrus neurons after single and intermittent limbic seizures [J].
Bengzon, J ;
Kokaia, Z ;
Elmer, E ;
Nanobashvili, A ;
Kokaia, M ;
Lindvall, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (19) :10432-10437
[12]   Normal timing of oligodendrocyte development from genetically engineered, lineage-selectable mouse ES cells [J].
Billon, N ;
Jolicoeur, C ;
Ying, QL ;
Smith, A ;
Raff, M .
JOURNAL OF CELL SCIENCE, 2002, 115 (18) :3657-3665
[13]   Embryonic stem cells develop into functional dopaminergic neurons after transplantation in a Parkinson rat model [J].
Björklund, LM ;
Sánchez-Pernaute, R ;
Chung, SM ;
Andersson, T ;
Chen, IYC ;
McNaught, KS ;
Brownell, AL ;
Jenkins, BG ;
Wahlestedt, C ;
Kim, KS ;
Isacson, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (04) :2344-2349
[14]  
BRISOCE J, 2002, CELL, V101, P435
[15]   In vitro-generated neural precursors participate in mammalian brain development [J].
Brüstle, O ;
Spiro, AC ;
Karram, K ;
Choudhary, K ;
Okabe, S ;
McKay, RDG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14809-14814
[16]   Chimeric brains generated by intraventricular transplantation of fetal human brain cells into embryonic rats [J].
Brüstle, O ;
Choudhary, K ;
Karram, K ;
Hüttner, A ;
Murray, K ;
Dubois-Dalcq, M ;
McKay, RDG .
NATURE BIOTECHNOLOGY, 1998, 16 (11) :1040-1044
[17]   Restoring production of hippocampal neurons in old age [J].
Cameron, HA ;
McKay, RDG .
NATURE NEUROSCIENCE, 1999, 2 (10) :894-897
[18]   Radial glia:: multi-purpose cells for vertebrate brain development [J].
Campbell, K ;
Götz, M .
TRENDS IN NEUROSCIENCES, 2002, 25 (05) :235-238
[19]   Regional incorporation and site-specific differentiation of striatal precursors transplanted to the embryonic forebrain ventricle [J].
Campbell, K ;
Olsson, M ;
Bjorklund, A .
NEURON, 1995, 15 (06) :1259-1273
[20]  
Carletti B, 2002, J NEUROSCI, V22, P7132