Synaptic vesicles: Test for a role in presynaptic calcium regulation

被引:37
作者
Macleod, GT [1 ]
Marin, L [1 ]
Charlton, MP [1 ]
Atwood, HL [1 ]
机构
[1] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A8, Canada
关键词
calcium regulation; calcium channels; synaptic vesicles; Drosophila; temperature-sensitive mutant; shibire;
D O I
10.1523/JNEUROSCI.5372-03.2004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Membrane-bound organelles such as mitochondria and the endoplasmic reticulum play an important role in neuronal Ca2+ homeostasis. Synaptic vesicles (SVs), the organelles responsible for exocytosis of neurotransmitters, occupy more of the volume of presynaptic nerve terminals than any other organelle and, under some conditions, can accumulate Ca2+. They are also closely associated with voltage-gated Ca2+ channels(VGCCs) that trigger transmitter releasebyadmitting Ca2+ into the nerve terminal in response to action potentials (APs). We tested the hypothesis that SVs can modulate Ca2+ signals in the presynaptic terminal. This has been a difficult question to address because neither pharmacological nor genetic approaches to block Ca2+ permeation of the SV membrane have been available. To investigate the possible role of SVs in Ca2+ regulation, we used imaging techniques to compare Ca2+ dynamics in motor nerve terminals before and after depletion of SVs. We used the temperature-sensitive Drosophila dynamin mutant shibire, in which SVs can be eliminated by stimulation. There was no difference in the amplitude or time course of Ca2+ responses during high-frequency trains of APs, or single APs, in individual presynaptic boutons before and after depletion of SVs. SVs have a limited role, if any, in the rapid sequestration of Ca2+ within the neuronal cytosol or the synaptic microdomain. We also conclude that SVs are not important for regulation of synaptic VGCCs.
引用
收藏
页码:2496 / 2505
页数:10
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