Neurotrophic and gliatrophic contexts in Drosophila

被引:17
作者
Hidalgo, Alicia [1 ]
Learte, Anabel R. [1 ]
McQuilton, Peter [1 ]
Pennack, Jenny [1 ]
Zhu, Bangfu [1 ]
机构
[1] Univ Birmingham, Sch Biosci, Neurodev Grp, Birmingham B15 2TT, W Midlands, England
基金
英国医学研究理事会;
关键词
Drosophila; neurotrophic factor; gliatrophic factor; neuregulin; neurotrophin; survival;
D O I
10.1159/000094086
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Trophic interactions in the vertebrate nervous system enable the adjustment of cell number and axon guidance, targeting and connectivity. Computational analysis of the sequenced Drosophila genome failed to identify some of the main trophic factors, the neuregulins and neurotrophins, as well as many other genes. This provoked speculations that the Drosophila nervous system might not require such regulative interactions. Here we review abundant cellular, genetic and functional data that demonstrate the existence of both neurotrophic and gliatrophic interactions in the Drosophila nervous system. Glial survival is maintained by the epidermal growth factor receptor (EGFR) signaling pathway in response to the ligands Spitz, a transforming growth factor-alpha (TGF-alpha) signaling molecule, and Vein, a neuregulin homologue. Cellular and genetic evidence predicts the existence of neuronal trophic factors operating at least in the Drosophila embryo during axon guidance and, in the visual system, during the targeting of retinal axons in the brain. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:173 / 180
页数:8
相关论文
共 57 条
[1]   Drosophila RET contains an active tyrosine kinase and elicits neurotrophic activities in mammalian cells [J].
Abrescia, C ;
Sjöstrand, D ;
Kjaer, S ;
Ibáñez, CF .
FEBS LETTERS, 2005, 579 (17) :3789-3796
[2]   Evolution of the GDNF family ligands and receptors [J].
Airaksinen, Matti S. ;
Holm, Liisa ;
Hatinen, Tuomas .
BRAIN BEHAVIOR AND EVOLUTION, 2006, 68 (03) :181-190
[3]   The EGF receptor defines domains of cell cycle progression and survival to regulate cell number in the developing Drosophila eye [J].
Baker, NE ;
Yu, SY .
CELL, 2001, 104 (05) :699-708
[4]   Cell proliferation, survival, and death in the Drosophila eye [J].
Baker, NE .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2001, 12 (06) :499-507
[5]   NEUROTROPHIC FACTORS - AN EVOLUTIONARY PERSPECTIVE [J].
BARDE, YA .
JOURNAL OF NEUROBIOLOGY, 1994, 25 (11) :1329-1333
[6]  
BELLO B, 2003, NEURON, V23, P185
[7]   Regulation of cell number by MAPK-dependent control of apoptosis: A mechanism for trophic survival signaling [J].
Bergmann, A ;
Tugentman, M ;
Shilo, BZ ;
Steller, H .
DEVELOPMENTAL CELL, 2002, 2 (02) :159-170
[8]  
Booth GE, 2000, DEVELOPMENT, V127, P237
[9]   The embryonic central nervous system lineages of Drosophila melanogaster .1. Neuroblast lineages derived from the ventral half of the neuroectoderm [J].
Bossing, T ;
Udolph, G ;
Doe, CQ ;
Technau, GM .
DEVELOPMENTAL BIOLOGY, 1996, 179 (01) :41-64
[10]   Deregulation of the Egfr/Ras signaling pathway induces age-related brain degeneration in the Drosophila mutant vap [J].
Botella, JA ;
Kretzschmar, D ;
Kiermayer, C ;
Feldmann, P ;
Hughes, DA ;
Schneuwly, S .
MOLECULAR BIOLOGY OF THE CELL, 2003, 14 (01) :241-250