Nanoscale organization of nicotinic acetylcholine receptors revealed by stimulated emission depletion microscopy

被引:101
作者
Kellner, R. R.
Baier, C. J.
Willig, K. I.
Hell, S. W. [1 ]
Barrantes, F. J.
机构
[1] Max Planck Inst Biophys Chem, Dept NanoBiophoton, D-37077 Gottingen, Germany
[2] UNESCO, Chair Biophys & Mol Neurobiol, RA-8000 Bahia Blanca, Buenos Aires, Argentina
[3] Inst Invest Bioquim, RA-8000 Bahia Blanca, Buenos Aires, Argentina
关键词
cyloskeleton; supramolecular aggregates; cholesterol; synapse; ion channel; STED microscopy;
D O I
10.1016/j.neuroscience.2006.08.071
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Acetylcholine receptor (AChR) supramolecular aggregates that have hitherto only been accessible to examination by electron microscopy were imaged with stimulated emission depletion (STED) fluorescence microscopy, providing resolution beyond limits of diffraction of classical widefield or confocal microscopes. We examined a Chinese hamster ovary cell liner CHO-K1/A5, that stably expresses adult murine AChR. Whereas confocal microscopy displays AChR clusters as diffraction-limited dots of similar to 200 nm diameter, STED microscopy yields nanoclusters; with a peak size distribution of similar to 55 rim. Utilizing this resolution, we show that cholesterol depletion by acute (30 min, 37 degrees C) exposure to methyl-beta-cyclodextrin alters the short and long range organization of AChR nanoclusters on the cell surface. In the short range, AChRs form larger nanoclusters, possibly related to the alteration of cholesterol-dependent protein-protein associations. Ripley's K-test on STED images reveals changes in nanocluster distribution on larger scales (0.5-3.5 mu m), which possibly are related to the abolition of cytoskeletal physical barriers preventing the lateral diffusion of AChR nanoclusters. (c) 2006 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:135 / 143
页数:9
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