Synaptophysin Is Required for Synaptobrevin Retrieval during Synaptic Vesicle Endocytosis

被引:95
|
作者
Gordon, Sarah L. [1 ]
Leube, Rudolf E. [2 ]
Cousin, Michael A. [1 ]
机构
[1] Univ Edinburgh, Membrane Biol Grp, Ctr Integrat Physiol, Edinburgh EH8 9XD, Midlothian, Scotland
[2] Rhein Westfal TH Aachen, Inst Mol & Cellular Anat, D-52074 Aachen, Germany
来源
JOURNAL OF NEUROSCIENCE | 2011年 / 31卷 / 39期
基金
英国惠康基金;
关键词
DI-LEUCINE MOTIF; COMPLEX; PROTEIN; LOCALIZATION; SYNAPSES; SNARE; EXOCYTOSIS; NEURONS; BINDING; MICE;
D O I
10.1523/JNEUROSCI.3162-11.2011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The integral synaptic vesicle (SV) protein synaptophysin forms similar to 10% of total SV protein content, but has no known function in SV physiology. Synaptobrevin (sybII) is another abundant integral SV protein with an essential role in SV exocytosis. Synaptophysin and sybII form a complex in nerve terminals, suggesting this interaction may have a key role in presynaptic function. To determine how synaptophysin controls sybII traffic in nerve terminals, we used a combination of optical imaging techniques in cultures derived from synaptophysin knock-out mice. We show that synaptophysin is specifically required for the retrieval of the pH-sensitive fluorescent reporter sybII-pHluorin from the plasma membrane during endocytosis. The retrieval of other SV protein cargo reporters still occurred; however, their recapture proceeded with slower kinetics. This slowing of SV retrieval kinetics in the absence of synaptophysin did not impact on global SV turnover. These results identify a specific and selective requirement for synaptophysin in the retrieval of sybII during SV endocytosis and suggest that their interaction may act as an adjustable regulator of SV retrieval efficiency.
引用
收藏
页码:14032 / 14036
页数:5
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