Neuronal development

被引:0
作者
Giehl, Klaus M. [1 ]
机构
[1] Univ Aarhus, Dept Biochem Med, DK-8000 Aarhus, Denmark
来源
NEURONAL ACTIVITY IN TUMOR TISSUE | 2007年 / 39卷
关键词
NERVE GROWTH-FACTOR; SONIC HEDGEHOG; NEUROTROPHIN RECEPTOR; CORTICOSPINAL NEURONS; CNS DEVELOPMENT; STEM-CELLS; ROLES; NOTCH; WNT; INDUCTION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Biological tools that are unleashed in malignancies are employed in a controlled manner during neuronal development. By default, early embryonic cells would become neuronal stem cells, a path that is blocked by specific signaling pathways. The future nervous system only develops where this blockade is inhibited by inductive signals from the 'organizer'. Once the future brain and spinal cord regions are determined, the mitotic potential in this region must be maintained long enough to produce all cells required, but also be controlled to avoid excessive over-production of cells. Newly generated cells must then migrate to their future destination, they must know where to settle down, and they must differentiate. To shape the developing nervous system and to adapt its functionality to the postnatal environment, cell survival must be regulated, i.e. survival of some cells is supported while death of others is induced. Thus, inductive events, proliferation, cell migration, differentiation, cell survival and cell death are highly regulated during neuronal development, while these functions are de-regulated in malignancies. The molecular pathways for neuronal development mutually modulate each other and are still present in the adult nervous system. Because many of these pathways are implicated in tumors, neurons may affect these conditions. Copyright (c) 2007 S. Karger AG, Basel.
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页码:1 / 29
页数:29
相关论文
共 73 条
[1]   BDNF regulates spontaneous correlated activity at early developmental stages by increasing synaptogenesis and expression of the K+/Cl- co-transporter KCC2 [J].
Aguado, F ;
Carmona, MA ;
Pozas, E ;
Aguiló, A ;
Martínez-Guijarro, FJ ;
Alcantara, S ;
Borrell, V ;
Yuste, R ;
Ibañez, CF ;
Soriano, E .
DEVELOPMENT, 2003, 130 (07) :1267-1280
[2]   The emergent design of the neural tube:: prepattern, SHH morphogan and GLI code [J].
Altaba, AR ;
Nguyên, V ;
Palma, V .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (05) :513-521
[3]  
[Anonymous], 1991, Principles of Neural Science
[4]  
Bandtlow C., 2004, Sci STKE, pp, DOI DOI 10.1126/STKE.2352004PE24
[5]   WHAT, IF ANYTHING, IS A NEUROTROPHIC FACTOR [J].
BARDE, YA .
TRENDS IN NEUROSCIENCES, 1988, 11 (08) :343-346
[6]   p75NTR is positively promiscuous: Novel partners and new insights [J].
Barker, PA .
NEURON, 2004, 42 (04) :529-533
[7]   Neurotrophins: key regulators of cell fate and cell shape in the vertebrate nervous system [J].
Bibel, M ;
Barde, YA .
GENES & DEVELOPMENT, 2000, 14 (23) :2919-2937
[8]   CHANGES IN CYTOSKELETAL PROTEIN-SYNTHESIS FOLLOWING AXON INJURY AND DURING AXON REGENERATION [J].
BISBY, MA ;
TETZLAFF, W .
MOLECULAR NEUROBIOLOGY, 1992, 6 (2-3) :107-123
[9]   Immune signalling in neural development, synaptic plasticity and disease [J].
Boulanger, LM ;
Shatz, CJ .
NATURE REVIEWS NEUROSCIENCE, 2004, 5 (07) :521-531
[10]   Multi-tasking by the p75 neurotrophin receptor: sortilin things out? [J].
Bronfman, FC ;
Fainzilber, M .
EMBO REPORTS, 2004, 5 (09) :867-871