Cyclin Y inhibits plasticity-induced AMPA receptor exocytosis and LTP

被引:18
作者
Cho, Eunsil [1 ,5 ]
Kim, Dong-Hyun [2 ]
Hur, Young-Na [1 ]
Whitcomb, Daniel J. [2 ,3 ]
Regan, Philip [2 ,3 ]
Hong, Jung-Hwa [1 ]
Kim, Hanna [1 ]
Suh, Young Ho [4 ]
Cho, Kwangwook [2 ,3 ]
Park, Mikyoung [1 ]
机构
[1] Korea Inst Sci & Technol, Ctr Funct Connect, Seoul 136791, South Korea
[2] Univ Bristol, Fac Med & Dent, Sch Clin Sci, Henry Wellcome Labs Integrat Neurosci & Endocrino, Bristol BS1 3NY, Avon, England
[3] Univ Bristol, Ctr Synapt Plast, Bristol BS1 3NY, Avon, England
[4] Seoul Natl Univ, Coll Med, Neurosci Res Inst, Dept Biomed Sci, Seoul 110799, South Korea
[5] Korea Univ Sci & Technol, Dept Neurosci, Taejon 305350, South Korea
基金
英国生物技术与生命科学研究理事会; 英国惠康基金; 新加坡国家研究基金会;
关键词
LONG-TERM POTENTIATION; CELL-CYCLE; GLUR1; SUBUNIT; SYNAPTIC-TRANSMISSION; PHOSPHORYLATION SITES; RECYCLING ENDOSOMES; DENDRITIC SPINES; CONSERVED CYCLIN; SILENT SYNAPSES; MYOSIN VB;
D O I
10.1038/srep12624
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
Cyclin Y (CCNY) is a member of the cyclin protein family, known to regulate cell division in proliferating cells. Interestingly, CCNY is expressed in neurons that do not undergo cell division. Here, we report that CCNY negatively regulates long-term potentiation (LTP) of synaptic strength through inhibition of AMPA receptor trafficking. CCNY is enriched in postsynaptic fractions from rat forebrain and is localized adjacent to postsynaptic sites in dendritic spines in rat hippocampal neurons. Using live-cell imaging of a pH-sensitive AMPA receptor, we found that during LTP-inducing stimulation, CCNY inhibits AMPA receptor exocytosis in dendritic spines. Furthermore, CCNY abolishes LTP in hippocampal slices. Taken together, our findings demonstrate that CCNY inhibits plasticity-induced AMPA receptor delivery to synapses and thereby blocks LTP, identifying a novel function for CCNY in post-mitotic cells.
引用
收藏
页数:13
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