Drosophila endosomal proteins hook and deep orange regulate synapse size but not synaptic vesicle recycling

被引:0
|
作者
Narayanan, R
Krämer, H
Ramaswami, M
机构
[1] Univ Arizona, Dept Mol & Cell Biol, Tucson, AZ 85721 USA
[2] Univ Arizona, Div Neurobiol, ARL, Tucson, AZ 85721 USA
[3] Univ Texas, SW Med Ctr, Ctr Basic Neurosci, Dallas, TX 75235 USA
[4] Univ Texas, SW Med Ctr, Dept Cell Biol, Dallas, TX 75235 USA
来源
JOURNAL OF NEUROBIOLOGY | 2000年 / 45卷 / 02期
关键词
endocytosis; cell adhesion; eye color; lysosomes; synaptic plasticity;
D O I
10.1002/1097-4695(20001105)45:2<105::AID-NEU5>3.0.CO;2-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To study the function of endosomes at synapses we analyzed the localization and function of two Drosophila endosomal proteins, Hook and Deep orange (Dor), at the larval neuromuscular junction, Hook, a negative regulator of endocytic trafficking, and Dor, a positive regulator of endocytic trafficking, are highly enriched at synapses, especially close to postsynaptic membranes. Mutations in hook (hk) and dor do not affect synaptic vesicle recycling, as assessed by electrophysiological analysis of synaptic transmission and behavioral studies of double mutants with shi(ts) mutations that alter vesicle recycling, However, hk and dor mutations alter the number of presynaptic varicosities (synapse size) in opposing ways, Synapse size is increased in hk(11) mutants and is decreased in dor(4) mutants. Double mutants for dor and hk show a dor-like phenotype, These effects on synapse size parallel known functions of Hook and Dor in endocytosis and strongly indicate a role for endocytic trafficking in the regulation of synapse size in vivo. Our observations suggest a model in which Hook and Dor function in later stages of endocytosis is essential for regulating synaptic plasma membrane composition but not synaptic vesicle recycling. (C) 2000 John Wiley & Sans, Inc.
引用
收藏
页码:105 / 119
页数:15
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