Dendrite-specific remodeling of Drosophila sensory neurons requires matrix metalloproteases, ubiquitin-proteasome, and ecdysone signaling

被引:172
作者
Kuo, CT
Jan, LY
Jan, YN
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94143 USA
关键词
metamorphosis; pruning; ecdysone receptor;
D O I
10.1073/pnas.0507393102
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
During neuronal maturation, dendrites develop from immature neurites into mature arbors. In response to changes in the environment, dendrites from certain mature neurons can undergo large-scale morphologic remodeling. Here, we show a group of Drosophila peripheral sensory neurons, the class IV dendritic arborization (C4da) neurons, that completely degrade and regrow their elaborate dendrites. Larval dendrites of C4da neurons are first severed from the soma-and subsequently degraded during metamorphosis. This process is controlled by both intracellular and extracellular mechanisms: The ecdysone pathway and ubiquitin-proteasome system (UPS) are cell-intrinsic signals that initiate dendrite breakage, and extracellular matrix metalloproteases are required to degrade the severed dendrites. Surprisingly, C4da neurons retain their axonal projections during concurrent dendrite degradation, despite activated ecdysone and UPS pathways. These results demonstrate that, in response to environmental changes, certain neurons have cell-intrinsic abilities to completely lose their dendrites but keep their axons and subsequently regrow their dendritic arbors.
引用
收藏
页码:15230 / 15235
页数:6
相关论文
共 40 条
[1]   Drosophila ecdysone receptor mutations reveal functional differences among receptor isoforms [J].
Bender, M ;
Imam, FB ;
Talbot, WS ;
Ganetzky, B ;
Hogness, DS .
CELL, 1997, 91 (06) :777-788
[2]  
BRAND AH, 1993, DEVELOPMENT, V118, P401
[3]   EcR isoforms in Drosophila:: testing tissue-specific requirements by targeted blockade and rescue [J].
Cherbas, L ;
Hu, X ;
Zhimulev, I ;
Belyaeva, E ;
Cherbas, P .
DEVELOPMENT, 2003, 130 (02) :271-284
[4]   Cortical rewiring and information storage [J].
Chklovskii, DB ;
Mel, BW ;
Svoboda, K .
NATURE, 2004, 431 (7010) :782-788
[5]   The ubiquitin proteasome system in neurodegenerative diseases: Sometimes the chicken, sometimes the egg [J].
Ciechanover, A ;
Brundin, P .
NEURON, 2003, 40 (02) :427-446
[6]   Dendritic arbor development and synaptogenesis [J].
Cline, HT .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (01) :118-126
[7]   Receptor trafficking and synaptic plasticity [J].
Collingridge, GL ;
Isaac, JTR ;
Wang, YT .
NATURE REVIEWS NEUROSCIENCE, 2004, 5 (12) :952-962
[8]   Ubiquitination-dependent mechanisms regulate synaptic growth and function [J].
DiAntonio, A ;
Haghighi, AP ;
Portman, SL ;
Lee, JD ;
Amaranto, AM ;
Goodman, CS .
NATURE, 2001, 412 (6845) :449-452
[9]   Control of dendritic branching and tiling by the tricornered-kinase/furry signaling pathway in Drosophila sensory neurons [J].
Emoto, K ;
He, Y ;
Ye, B ;
Grueber, WB ;
Adler, PN ;
Jan, LY ;
Jan, YN .
CELL, 2004, 119 (02) :245-256
[10]   Genes regulating dendritic outgrowth, branching, and routing in Drosophila [J].
Gao, FB ;
Brenman, JE ;
Jan, LY ;
Jan, YN .
GENES & DEVELOPMENT, 1999, 13 (19) :2549-2561