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2
Spontaneous and evoked release are independently regulated at individual active zones.自发释放和诱发释放在各个活性区独立调节。
J Neurosci. 2013 Oct 30;33(44):17253-63. doi: 10.1523/JNEUROSCI.3334-13.2013.
3
Physiological recordings of high and low output NMJs on the crayfish leg extensor muscle.小龙虾腿部伸肌上高输出和低输出神经肌肉接头的生理记录。
J Vis Exp. 2010 Nov 17(45):2319. doi: 10.3791/2319.
4
Rab3a-mediated vesicle recruitment regulates short-term plasticity at the mouse diaphragm synapse.Rab3a介导的囊泡募集调节小鼠膈肌突触的短期可塑性。
Mol Cell Neurosci. 2009 Jun;41(2):286-96. doi: 10.1016/j.mcn.2009.03.008. Epub 2009 Apr 5.
5
Drosophila larval NMJ dissection.果蝇幼虫神经肌肉接头解剖。
J Vis Exp. 2009 Feb 4(24):1107. doi: 10.3791/1107.
6
Electrophysiological methods for recording synaptic potentials from the NMJ of Drosophila larvae.用于记录果蝇幼虫神经肌肉接头处突触电位的电生理方法。
J Vis Exp. 2009 Feb 6(24):1109. doi: 10.3791/1109.
7
Enhancement of the endosomal endocytic pathway increases quantal size.内体胞吞途径的增强会增加量子大小。
Mol Cell Neurosci. 2009 Feb;40(2):199-206. doi: 10.1016/j.mcn.2008.10.005. Epub 2008 Nov 5.
8
FM 1-43 labeling of synaptic vesicle pools at the Drosophila neuromuscular junction.果蝇神经肌肉接头处突触小泡池的FM 1-43标记
Methods Mol Biol. 2008;440:349-69. doi: 10.1007/978-1-59745-178-9_26.
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Making quantal analysis more convenient, fast, and accurate: user-friendly software QUANTAN.让定量分析更便捷、快速且准确:用户友好型软件QUANTAN。
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10
Synapsin maintains the reserve vesicle pool and spatial segregation of the recycling pool in Drosophila presynaptic boutons.突触结合蛋白维持果蝇突触前终扣中储备囊泡池和循环池的空间隔离。
Brain Res. 2007 Oct 31;1178:52-64. doi: 10.1016/j.brainres.2007.08.042. Epub 2007 Aug 24.

果蝇幼虫神经肌肉接头突触电流的局灶性大膜片钳记录

Focal Macropatch Recordings of Synaptic Currents from the Drosophila Larval Neuromuscular Junction.

作者信息

Vasin Alexander, Bykhovskaia Maria

机构信息

Department of Neurology, School of Medicine, Wayne State University.

Department of Neurology, School of Medicine, Wayne State University; Department of Anatomy and Cell Biology, School of Medicine, Wayne State University;

出版信息

J Vis Exp. 2017 Sep 25(127):56493. doi: 10.3791/56493.

DOI:10.3791/56493
PMID:28994789
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5752324/
Abstract

Drosophila neuromuscular junction (NMJ) is an excellent model system to study glutamatergic synaptic transmission. We describe the technique of focal macropatch recordings of synaptic currents from visualized boutons at the Drosophila larval NMJ. This technique requires customized fabrication of recording micropipettes, as well as a compound microscope equipped with a high magnification, long-distance water immersion objective, differential interference contrast (DIC) optics, and a fluorescent attachment. The recording electrode is positioned on the top of a selected synaptic bouton visualized with DIC optics, epi-fluorescence, or both. The advantage of this technique is that it allows monitoring the synaptic activity of a limited number of sites of release. The recording electrode has a diameter of several microns, and the release sites positioned outside of the electrode rim do not significantly affect the recorded currents. The recorded synaptic currents have fast kinetics and can be readily resolved. These advantages are especially important for the studies of mutant fly lines with enhanced spontaneous or asynchronous synaptic activity.

摘要

果蝇神经肌肉接头(NMJ)是研究谷氨酸能突触传递的优秀模型系统。我们描述了从果蝇幼虫NMJ处可视化的突触小体进行突触电流的局灶性大膜片钳记录技术。该技术需要定制记录微电极,以及配备高倍、长距离水浸物镜、微分干涉对比(DIC)光学系统和荧光附件的复合显微镜。记录电极位于通过DIC光学系统、落射荧光或两者同时观察到的选定突触小体顶部。该技术的优点是能够监测有限数量释放位点的突触活动。记录电极直径为几微米,位于电极边缘之外的释放位点不会对记录的电流产生显著影响。记录的突触电流具有快速动力学特性,并且易于分辨。这些优点对于研究具有增强的自发或异步突触活动的突变果蝇品系尤为重要。