The use of formic acid to embellish amyloid plaque detection in Alzheimer's disease tissues misguides key observations

被引:39
作者
D'Andrea, MR [1 ]
Reiser, PA [1 ]
Polkovitch, DA [1 ]
Gumula, NA [1 ]
Branchide, B [1 ]
Hertzog, BM [1 ]
Schmidheiser, D [1 ]
Belkowski, S [1 ]
Gastard, MC [1 ]
Andrade-Gordon, P [1 ]
机构
[1] Johnson & Johnson Pharmaceut Res & Dev, Drug Discovery, Spring House, PA 19477 USA
关键词
Alzheimer's disease; amyloid plaques; a beta 42; formic acid; immunohistochemistry; intracellular amyloid; neurons;
D O I
10.1016/S0304-3940(03)00252-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We compared our heat pretreatment method to the widely used formic acid pretreatment technique to immunohistochemically detect amyloid in control and Alzheimer's disease brain tissues. Both methods detected amyloid in plaques, neurons, ependymal cells, circulating monocytes, vascular smooth muscle and endothelial cells. Although there were no observable differences in the intensity of the amyloid labeling in these cell types using both pretreatment methods, there were considerable differences in the intensity of amyloid immunolabeling in the plaques. The formic acid produced much more intense amyloid labeling in the plaques than the heat method. With the heat method, the intensity of the amyloid labeling in the plaques was similar to that detected in nearby neurons suggesting a neuronal origin of plaques. Conversely, the intensity of the amyloid in nearby neurons and plaques was drastically different using the formic acid suggesting unique origins of amyloid. The obvious benefits of formic acid for increasing the sensitivity of amyloid plaque immunolabeling may artifactually emphasize plaques over amyloid-containing cells during analyses. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:114 / 118
页数:5
相关论文
共 19 条
[11]  
IKEDA S, 1989, LAB INVEST, V60, P113
[12]   DEMONSTRATION OF CRP IMMUNOREACTIVITY IN BRAINS OF ALZHEIMERS-DISEASE - IMMUNOHISTOCHEMICAL STUDY USING FORMIC-ACID PRETREATMENT OF TISSUE-SECTIONS [J].
IWAMOTO, N ;
NISHIYAMA, E ;
OHWADA, J ;
ARAI, H .
NEUROSCIENCE LETTERS, 1994, 177 (1-2) :23-26
[13]  
KITAMOTO T, 1987, LAB INVEST, V57, P230
[14]   Microwave treatment enhances the immunostaining of amyloid deposits in both the transmissible and non-transmissible brain amyloidoses [J].
Liberski, PP ;
Yanagihara, R ;
Brown, P ;
Kordek, R ;
Kloszewska, I ;
Bratosiewicz, J ;
Gajdusek, DC .
NEURODEGENERATION, 1996, 5 (01) :95-99
[15]  
NAGELE RG, 2003, IN PRESS BRAIN RES
[16]  
Takeda A, 1998, LAB INVEST, V78, P1169
[17]  
VINTERS HV, 1988, AM J PATHOL, V133, P150
[18]   Cerebellar diffuse amyloid plaques are derived from dendritic Aβ42 accumulations in Purkinje cells [J].
Wang, HY ;
D'Andrea, MR ;
Nagele, RG .
NEUROBIOLOGY OF AGING, 2002, 23 (02) :213-223
[19]   Selective cytotoxicity of intracellular amyloid β peptide1-42 through p53 and Bax in cultured primary human neurons [J].
Zhang, Y ;
McLaughlin, R ;
Goodyer, C ;
LeBlanc, A .
JOURNAL OF CELL BIOLOGY, 2002, 156 (03) :519-529