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Intracellular Electrochemical Nanomeasurements Reveal that Exocytosis of Molecules at Living Neurons is Subquantal and Complex
Author(s) -
Larsson Anna,
Majdi Soodabeh,
Oleinick Alexander,
Svir Irina,
Dunevall Johan,
Amatore Christian,
Ewing Andrew G.
Publication year - 2020
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201914564
Subject(s) - exocytosis , vesicle , biophysics , amperometry , chemistry , synaptic vesicle , chromaffin cell , neuron , vesicle fusion , depolarization , neuroscience , biology , adrenal medulla , membrane , biochemistry , electrochemistry , catecholamine , electrode
Since the early work of Bernard Katz, the process of cellular chemical communication through exocytosis, quantal release, has been considered to be all or none. Recent evidence has shown exocytosis to be partial or “subquantal” at single‐cell model systems, but there is a need to understand this at communicating nerve cells. Partial release allows nerve cells to control the signal at the site of release during individual events, for which the smaller the fraction released, the greater the range of regulation. Herein, we show that the fraction of the vesicular octopamine content released from a living Drosophila larval neuromuscular neuron is very small. The percentage of released molecules was found to be only 4.5 % for simple events and 10.7 % for complex (i.e., oscillating or flickering) events. This large content, combined with partial release controlled by fluctuations of the fusion pore, offers presynaptic plasticity that can be widely regulated.