PSD95 nanoclusters are postsynaptic building blocks in hippocampus circuits

被引:109
作者
Broadhead, Matthew J. [1 ,2 ]
Horrocks, Mathew H. [3 ]
Zhu, Fei [1 ]
Muresan, Leila [4 ]
Benavides-Piccione, Ruth [5 ,6 ]
DeFelipe, Javier [5 ,6 ]
Fricker, David [7 ]
Kopanitsa, Maksym V. [7 ,9 ]
Duncan, Rory R. [2 ,8 ]
Klenerman, David [3 ]
Komiyama, Noboru H. [1 ]
Lee, Steven F. [3 ]
Grant, Seth G. N. [1 ]
机构
[1] Univ Edinburgh, CCBS, Edinburgh, Midlothian, Scotland
[2] Heriot Watt Univ, ESRIC, Edinburgh, Midlothian, Scotland
[3] Univ Cambridge, Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England
[4] Univ Cambridge, CAIC, Cambridge, England
[5] Inst Cajal CSIC, Madrid, Spain
[6] Ctr Tecnol Biomed UPM, Madrid, Spain
[7] Synome Ltd, Babraham Res Campus, Cambridge, England
[8] Heriot Watt Univ, Inst Biol Chem Biophys & Bioengn, Edinburgh EH14 4AS, Midlothian, Scotland
[9] Charles River Discovery Res Serv, Kuopio 70210, Finland
基金
英国惠康基金; 英国医学研究理事会;
关键词
LONG-TERM POTENTIATION; SYNAPTIC-TRANSMISSION; AXOSPINOUS SYNAPSES; SPINE FORMATION; AMPA RECEPTORS; PSD-95; DENSITY; MULTIPLE; CA1; COMPLEXES;
D O I
10.1038/srep24626
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
The molecular features of synapses in the hippocampus underpin current models of learning and cognition. Although synapse ultra-structural diversity has been described in the canonical hippocampal circuitry, our knowledge of sub-synaptic organisation of synaptic molecules remains largely unknown. To address this, mice were engineered to express Post Synaptic Density 95 protein (PSD95) fused to either eGFP or mEos2 and imaged with two orthogonal super-resolution methods: gated stimulated emission depletion (g-STED) microscopy and photoactivated localisation microscopy (PALM). Large-scale analysis of similar to 100,000 synapses in 7 hippocampal sub-regions revealed they comprised discrete PSD95 nanoclusters that were spatially organised into single and multi-nanocluster PSDs. Synapses in different sub-regions, cell-types and locations along the dendritic tree of CA1 pyramidal neurons, showed diversity characterised by the number of nanoclusters per synapse. Multi-nanocluster synapses were frequently found in the CA3 and dentate gyrus sub-regions, corresponding to large thorny excrescence synapses. Although the structure of individual nanoclusters remained relatively conserved across all sub-regions, PSD95 packing into nanoclusters also varied between sub-regions determined from nanocluster fluorescence intensity. These data identify PSD95 nanoclusters as a basic structural unit, or building block, of excitatory synapses and their number characterizes synapse size and structural diversity.
引用
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页数:14
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