Zinc Regulates Chemical-Transmitter Storage in Nanometer Vesicles and Exocytosis Dynamics as Measured by Amperometry.

Zinc Regulates Chemical-Transmitter Storage in Nanometer Vesicles and Exocytosis Dynamics as Measured by Amperometry.
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DOI:
10.1002/anie.201700095
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发表时间:
2017-04-24
期刊:
Angewandte Chemie (International ed. in English)
影响因子:
--
通讯作者:
Ewing AG
Ewing AG
中科院分区:
其他
文献类型:
--
作者:
Ren L;Pour MD;Majdi S;Li X;Malmberg P;Ewing AG

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We applied electrochemical techniques with nano-tip electrodes to show that micromolar concentrations of zinc not only trigger changes in the dynamics of exocytosis, but also vesicle content in a model cell line. The vesicle catecholamine content in PC12 cells is significantly decreased after 100 μM zinc treatment, but, catecholamine release during exocytosis remains nearly the same. This contrasts the number of molecules stored in the exocytosis vesicles, which decreases, and we find that the amount of catecholamine released from zinc-treated cells reaches nearly 100 percent content being expelled. Further investigation shows that zinc slows down exocytotic release allowing time for this to occur. Our results provide the missing link between zinc and the regulation of neurotransmitter release processes, which might be important in memory formation and storage. We have employed single cell amperometry and intracellular vesicle impact electrochemical cytometry to investigate the effects of zinc on exocytosis and vesicle content in PC12 cells. Our results show that zinc not only changes the transmitter storage, but also the exocytosis dynamics by leading a more stable fusion pore opening and closing process.
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