Comparative analysis of an improved thioflavin-S stain, Gallyas silver stain, and immunohistochemistry for neurofibrillary tangle demonstration on the same sections

被引:111
作者
Sun, AY [1 ]
Nguyen, XV [1 ]
Bing, GY [1 ]
机构
[1] Univ Kentucky, Dept Anat & Neurobiol, Ctr Med, Lexington, KY 40536 USA
关键词
Alzheimer's disease; neurofibrillary tangles; transentorhinal cortex; thioflavin S; silver staining; immunohistochemistry;
D O I
10.1177/002215540205000403
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
An improved thioflavin-S stain, Gallyas silver stain, and two immunostainings were quantitatively compared for demonstration of neurofibrillary tangles (NFTs) on the same sections. Sections of hippocampal formation from seven cases of Alzheimer's disease (AD) were immunofluorescently stained with a commercially available polyclonal NFT antibody or a PHF-1 monoclonal antibody, followed by an improved thioflavin-S stain, and finally by Gallyas silver staining. The thioflavin-S method was improved by using a combination quenching method that removes background autofluorescence without remarkable tissue damage and by post-treatment with concentrated phosphate buffer, which minimizes photobleaching. PHF-1 or NFT immunostaining is much less sensitive than the improved thioflavin-S staining and Gallyas silver staining, particularly in the transentorhinal region. Moreover PHF-1 immunoreactivity varied greatly among AD individuals. Thioflavin-S staining and Gallyas silver staining show almost the same sensitivity in NFT demonstration, but only the former depends on the secondary protein structure of NFTs. This study suggests that the improved thioflavin-S staining is a simple, sensitive, and consistent method for demonstration of neurofibrillary pathology.
引用
收藏
页码:463 / 472
页数:10
相关论文
共 30 条
[1]   Hyperphosphorylation induces self-assembly of τ into tangles of paired helical filaments/straight filaments [J].
Alonso, AD ;
Zaidi, T ;
Novak, M ;
Grundke-Iqbal, I ;
Iqbal, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (12) :6923-6928
[2]  
BONDAREFF W, 1995, J NEUROPATH EXP NEUR, V54, P657, DOI 10.1097/00005072-199509000-00007
[3]   THE HUMAN ENTORHINAL CORTEX - NORMAL MORPHOLOGY AND LAMINA-SPECIFIC PATHOLOGY IN VARIOUS DISEASES [J].
BRAAK, H ;
BRAAK, E .
NEUROSCIENCE RESEARCH, 1992, 15 (1-2) :6-31
[4]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[5]   FORMIC-ACID TREATMENT EXPOSES HIDDEN NEUROFILAMENT AND TAU EPITOPES IN ABNORMAL CYTOSKELETAL FILAMENTS FROM PATIENTS WITH PROGRESSIVE SUPRANUCLEAR PALSY AND ALZHEIMERS-DISEASE [J].
CAMMARATA, S ;
MANCARDI, G ;
TABATON, M .
NEUROSCIENCE LETTERS, 1990, 115 (2-3) :351-355
[6]   Improved selectivity and sensitivity in the visualization of neurofibrillary tangles, plaques and neuropil threads [J].
Cullen, KM ;
Halliday, GM ;
Cartwright, H ;
Kril, JJ .
NEURODEGENERATION, 1996, 5 (02) :177-187
[7]   The biochemical pathway of neurofibrillary degeneration in aging and Alzheimer's disease [J].
Delacourte, A ;
David, JP ;
Sergeant, N ;
Buée, L ;
Wattez, A ;
Vermersch, P ;
Ghozali, F ;
Fallet-Bianco, C ;
Pasquier, F ;
Lebert, F ;
Petit, H ;
Di Menza, C .
NEUROLOGY, 1999, 52 (06) :1158-1165
[8]  
DICKSON DW, 1992, ACTA NEUROPATHOL, V84, P596
[9]   LACK OF THE CARBOXYL TERMINAL SEQUENCE OF TAU IN GHOST TANGLES OF ALZHEIMERS-DISEASE [J].
ENDOH, R ;
OGAWARA, M ;
IWATSUBO, T ;
NAKANO, I ;
MORI, H .
BRAIN RESEARCH, 1993, 601 (1-2) :164-172
[10]  
GALLYAS F, 1971, ACTA MORPHOL HUNG, V19, P1