Super-resolution imaging of synaptic and Extra-synaptic AMPA receptors with different-sized fluorescent probes

被引:66
作者
Lee, Sang Hak [1 ,2 ]
Jin, Chaoyi [1 ,2 ]
Cai, En [1 ,2 ,6 ]
Ge, Pinghua [1 ,2 ]
Ishitsuka, Yuji [1 ,2 ]
Teng, Kai Wen [1 ,2 ]
de Thomaz, Andre A. [1 ,2 ,7 ]
Nall, Duncan [1 ,2 ]
Baday, Murat [1 ,2 ]
Jeyifous, Okunola [3 ,4 ]
Demonte, Daniel [5 ]
Dundas, Christopher M. [5 ,8 ]
Park, Sheldon [5 ]
Delgado, Jary Y. [3 ,4 ]
Green, William N. [3 ,4 ]
Selvin, Paul R. [1 ,2 ]
机构
[1] Univ Illinois, Dept Phys, Ctr Biophys & Quantitat Biol, Champaign, IL 61820 USA
[2] Univ Illinois, Ctr Phys Living Cells, Champaign, IL 61820 USA
[3] Univ Chicago, Dept Neurobiol, Chicago, IL 60637 USA
[4] Marine Biol Lab, Chicago, IL USA
[5] Univ Buffalo, Dept Chem & Biol Engn, Buffalo, NY USA
[6] Univ Calif San Francisco, San Francisco, CA 94143 USA
[7] Univ Estadual Campinas, Inst Phys Gleb Wataghin, Campinas, SP, Brazil
[8] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
SMALL QUANTUM DOTS; EXTRACELLULAR-MATRIX; NEUROTRANSMITTER RECEPTOR; STREPTAVIDIN MONOMER; RECYCLING ENDOSOMES; LIVING CELLS; TRAFFICKING; SYNAPSES; PLASTICITY; DIFFUSION;
D O I
10.7554/eLife.27744
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Previous studies tracking AMPA receptor (AMPAR) diffusion at synapses observed a large mobile extrasynaptic AMPAR pool. Using super-resolution microscopy, we examined how fluorophore size and photostability affected AMPAR trafficking outside of, and within, post-synaptic densities (PSDs) from rats. Organic fluorescent dyes(>= 4 nm), quantum dots, either small (>= 10 nm diameter; sQDs) or big (>20 nm; bQDs), were coupled to AMPARs via different-sized linkers. We find that >90% of AMPARs labeled with fluorescent dyes or sQDs were diffusing in confined nanodomains in PSDs, which were stable for 15 min or longer. Less than 10% of sQD-AMPARs were extrasynaptic and highly mobile. In contrast, 5-10% of bQD-AMPARs were in PSDs and 90-95% were extrasynaptic as previously observed. Contrary to the hypothesis that AMPAR entry is limited by the occupancy of open PSD 'slots', our findings suggest that AMPARs rapidly enter stable nanodomains in PSDs with lifetime >15 min, and do not accumulate in extrasynaptic membranes.
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页数:26
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