STED imaging of tau filaments in Alzheimer's disease cortical grey matter

被引:15
|
作者
Benda, Ales [2 ,3 ]
Aitken, Hayden [1 ]
Davies, Danielle S. [1 ]
Whan, Renee [2 ]
Goldsbury, Claire [1 ]
机构
[1] Univ Sydney, Sch Med Sci, Discipline Anat & Histol, Sydney, NSW 2006, Australia
[2] Univ New South Wales, Biomed Imaging Facil, Sydney, NSW, Australia
[3] Charles Univ Prague, Fac Sci, BIOCEV, Imaging Methods Core Facil, Prague, Czech Republic
基金
澳大利亚国家健康与医学研究理事会;
关键词
STED; Super resolution; Human tissue; Alzheimer's disease; AD; Tau protein; Tau filament; PHF; SUPERRESOLUTION MICROSCOPY; DEGENERATION; PATHOLOGY; AGGREGATION; NANOSCALE; PLASTICITY; SYNAPSES; TOXICITY; FIBRILS; TANGLES;
D O I
10.1016/j.jsb.2016.07.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) involves the propagation of filaments of tau protein throughout the cerebral cortex. Imaging tau filaments and oligomers in human brain at high resolution would help contribute insight into the mechanism and progression of tauopathic diseases. STED microscopy is a nano-scale imaging technique and we aimed to test the abilities of this method for resolving tau structures within human brain. Using autopsied 50 mu m AD brain sections, we demonstrate that STED microscopy can resolve immunolabelled tau filaments at 77 nm resolution. Ribbon-like tau filaments imaged by STED appeared smooth along their axis with limited axial undulations. STED also resolved 70-80 nm wide tau puncta. Of the fluorophores tested, STAR635p was optimal for STED imaging in this tissue. This was in part due to brain tissue autofluorescence within the lower wavelength ranges (488-590 nm). Further, the stability and minimal photo bleaching of STAR635p allowed STED z-stacks of neurons packed with tau filaments (neurofibrillary tangles) to be collated. There was no loss of x-y image resolution of individual tau filaments through the 20 mu m z-stack. This demonstrates that STED can contribute to nano-scale analysis and characterisation of pathologies within banked human autopsied brain tissue. Resolving tau structures at this level of resolution provides promising avenues for understanding mechanisms of pathology propagation in the different tauopathies as well as illuminating what contributes to disease heterogeneity. (C) 2016 Published by Elsevier Inc.
引用
收藏
页码:345 / 352
页数:8
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