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Dynamin I phosphorylation by GSK3 controls activity-dependent bulk endocytosis of synaptic vesicles
被引:133
|作者:
Clayton, Emma L.
[1
]
Sue, Nancy
[2
]
Smillie, Karen J.
[1
]
O'Leary, Timothy
[1
]
Bache, Nicolai
[2
]
Cheung, Giselle
[1
]
Cole, Adam R.
[3
]
Wyllie, David J.
[1
]
Sutherland, Calum
[3
]
Robinson, Phillip J.
[2
]
Cousin, Michael A.
[1
]
机构:
[1] Univ Edinburgh, Ctr Integrat Physiol, Edinburgh, Midlothian, Scotland
[2] Univ Sydney, Childrens Med Res Inst, Sydney, NSW 2006, Australia
[3] Univ Dundee, Ninewells Hosp & Med Sch, Biomed Res Inst, Dundee DD1 9SY, Scotland
基金:
英国惠康基金;
英国医学研究理事会;
澳大利亚国家健康与医学研究理事会;
关键词:
GLYCOGEN-SYNTHASE KINASE-3;
MEMBRANE RETRIEVAL;
STIMULATION;
INHIBITORS;
DISCOVERY;
CDK5;
VIVO;
WNT;
D O I:
10.1038/nn.2571
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Glycogen synthase kinase 3 (GSK3) is a critical enzyme in neuronal physiology; however, it is not yet known whether it has any specific role in presynaptic function. We found that GSK3 phosphorylates a residue on the large GTPase dynamin I (Ser-774) both in vitro and in primary rat neuronal cultures. This was dependent on prior phosphorylation of Ser-778 by cyclin-dependent kinase 5. Using both acute inhibition with pharmacological antagonists and silencing of expression with short hairpin RNA, we found that GSK3 was specifically required for activity-dependent bulk endocytosis (ADBE) but not clathrin-mediated endocytosis. Moreover we found that the specific phosphorylation of Ser-774 on dynamin I by GSK3 was both necessary and sufficient for ADBE. These results demonstrate a presynaptic role for GSK3 and they indicate that a protein kinase signaling cascade prepares synaptic vesicles for retrieval during elevated neuronal activity.
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页码:845 / U85
页数:9
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