Electrical Stimulation: FM Dye Loading and Unloading
4:08
Channelrhodopsin Stimulation: FM Dye Loading and Unloading
5:21
Fluorescence Quantification
6:12
Results: Synaptic Ultrastructure with FM Dye Photoconversion to Mark Vesicles
7:22
Conclusion
副本
The overall goal of this experiment is to observe the endo and exocytosis cycling of synaptic vesicles on the live preparation of Drosophila larval neuromuscular junction using fluorescent FM dyes. This method can help answer key questions in the
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Synaptic vesicle (SV) cycling is the core mechanism of intercellular communication at neuronal synapses. FM dye uptake and release are the primary means of quantitatively assaying SV endo- and exocytosis. Here, we compare all the stimulation methods to drive FM1-43 cycling at the Drosophila neuromuscular junction (NMJ) model synapse.