Synapsin II desynchronizes neurotransmitter release at inhibitory synapses by interacting with presynaptic calcium channels

被引:71
|
作者
Medrihan, Lucian [1 ,2 ]
Cesca, Fabrizia [1 ]
Raimondi, Andrea [1 ]
Lignani, Gabriele [1 ]
Baldelli, Pietro [1 ,2 ]
Benfenati, Fabio [1 ,2 ]
机构
[1] Ist Italiano Tecnol, Dept Neurosci & Brain Technol, I-16163 Genoa, Italy
[2] Univ Genoa, Dept Expt Med, I-16132 Genoa, Italy
来源
NATURE COMMUNICATIONS | 2013年 / 4卷
关键词
ASYNCHRONOUS TRANSMITTER RELEASE; CULTURED HIPPOCAMPAL-NEURONS; SYNAPTIC VESICLES; GABA RELEASE; SYNAPTOTAGMIN-I; GRANULE CELLS; CA2+ SENSOR; DOMAIN-E; TRANSMISSION; EPILEPSY;
D O I
10.1038/ncomms2515
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the central nervous system, most synapses show a fast mode of neurotransmitter release known as synchronous release followed by a phase of asynchronous release, which extends over tens of milliseconds to seconds. Synapsin II (SYN2) is a member of the multigene synapsin family (SYN1/2/3) of synaptic vesicle phosphoproteins that modulate synaptic transmission and plasticity, and are mutated in epileptic patients. Here we report that inhibitory synapses of the dentate gyrus of Syn II knockout mice display an upregulation of synchronous neurotransmitter release and a concomitant loss of delayed asynchronous release. Syn II promotes g-aminobutyric acid asynchronous release in a Ca2+-dependent manner by a functional interaction with presynaptic Ca2+ channels, revealing a new role in synaptic transmission for synapsins.
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页数:13
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