LR WHITE EMBEDDING ALLOWS A MULTIMETHOD APPROACH TO THE ANALYSIS OF BRAIN-TISSUE FROM PATIENTS WITH ALZHEIMERS-DISEASE

被引:17
|
作者
SINGHRAO, S
COLE, G
HENDERSON, WJ
NEWMAN, GR
机构
[1] UNIV COLL CARDIFF,ELECTRON MICROSCOPY UNIT,CARDIFF CF4 4XN,S GLAM,WALES
[2] UNIV COLL CARDIFF,TENOVUS INST CANC RES,CARDIFF CF4 4XN,S GLAM,WALES
[3] UNIV HOSP WALES,DEPT PATHOL,NEUROPATHOL UNIT,CARDIFF CF4 4XN,S GLAM,WALES
来源
HISTOCHEMICAL JOURNAL | 1990年 / 22卷 / 05期
关键词
D O I
10.1007/BF01387181
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Light (LM) and electron (EM) microscope comparisons of the cytochemistry and immunocytochemistry of neuritic plaques and neurofibrillary tangles, the main histopathological changes in the brains of Alzheimer's disease sufferers, have been almost impossible because of the disparity between the two technologies. By embedding unosmicated brain tissue in the acrylic resin LR White, direct comparisons can be made between techniques applied at the LM level with those at the EM level. After partial dehydration in 70% ethanol, the tissue is embedded by rapid infiltration and polymerization at 0°C, which has been shown to maximally preserve tissue immunoreactivity. Semithin sections are then receptive to routine LM stains, silver stains e.g. Gomori's methenamine silver, and immunocytochemistry with immunoperoxidase or immunocolloidal gold. Serial thin from the use of a mouse monoclonal antibody against β-amyloid and a rabbit polyclonal antibody against ubiquitin are presented. LR White resin includes no elements other than carbon, oxygen and nitrogen, of which it is composed, so that sections of it are valuable for sensitive X-ray energy dispersive microanalysis. © 1990 Chapman and Hall Ltd.
引用
收藏
页码:257 / 268
页数:12
相关论文
共 50 条
  • [1] DOLICHOLS ARE ELEVATED IN BRAIN-TISSUE FROM ALZHEIMERS-DISEASE, BUT NOT IN URINARY SEDIMENT FROM ALZHEIMERS-DISEASE AND DOWNS-SYNDROME
    WOLFE, LS
    KIN, NMKNY
    PALO, J
    BERGERON, C
    KOTILA, M
    VARONEN, S
    NEUROCHEMICAL PATHOLOGY, 1985, 3 (04): : 213 - 221
  • [2] REDUCED PHOSPHOLIPASE-D ACTIVITY IN BRAIN-TISSUE SAMPLES FROM ALZHEIMERS-DISEASE PATIENTS
    KANFER, JN
    HATTORI, H
    ORIHEL, D
    ANNALS OF NEUROLOGY, 1986, 20 (02) : 265 - 267
  • [3] ALTERED GENE-EXPRESSION IN ALZHEIMERS-DISEASE BRAIN-TISSUE
    MAY, PC
    JOHNSON, SA
    POIRIER, J
    LAMPERTETCHELLS, M
    FINCH, CE
    CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1989, 16 (04) : 473 - 476
  • [4] DEMONSTRATING IMMUNE-RELATED ANTIGENS IN ALZHEIMERS-DISEASE BRAIN-TISSUE
    ROGERS, J
    MUFSON, EJ
    NEUROBIOLOGY OF AGING, 1990, 11 (04) : 477 - 479
  • [5] POSSIBLE ENZYMATIC CAUSES FOR ELEVATED PHOSPHOMONOESTERS IN ALZHEIMERS-DISEASE BRAIN-TISSUE
    KANFER, JN
    PETTEGREW, JW
    MOOSSY, J
    MCCARTNEY, DG
    BIN, Q
    STRYCHOR, S
    MCKEAG, DW
    ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1991, 640 : 118 - 121
  • [6] POSTEMBEDDING STAINING OF BRAIN-TISSUE FOR ULTRASTRUCTURAL VISUALIZATION OF AMYLOID IN ALZHEIMERS-DISEASE
    MIGHELI, A
    ATTANASIO, A
    GIORDANA, MT
    BIOTECHNIC & HISTOCHEMISTRY, 1993, 68 (02) : 117 - 121
  • [7] IMMUNOAFFINITY PURIFICATION OF A4-RELATED PROTEINS FROM ALZHEIMERS-DISEASE BRAIN-TISSUE
    SMITH, MA
    CLARKE, K
    KIDD, M
    LANDON, M
    BIOCHEMICAL SOCIETY TRANSACTIONS, 1989, 17 (02) : 359 - 359
  • [8] BIOCHEMICAL-CHARACTERIZATION OF CARNITINE ACYLTRANSFERASES AND CARNITINE METABOLITES IN BRAIN-TISSUE OF PATIENTS WITH ALZHEIMERS-DISEASE
    MAURER, I
    ZEITSCHRIFT FUR GERONTOLOGIE UND GERIATRIE, 1995, 28 (03): : 229 - 229
  • [9] ALZHEIMERS-DISEASE - CHOLINE-ACETYLTRANSFERASE ACTIVITY IN BRAIN-TISSUE FROM CLINICAL AND PATHOLOGICAL SUBGROUPS
    BIRD, TD
    STRANAHAN, S
    SUMI, SM
    RASKIND, M
    ANNALS OF NEUROLOGY, 1983, 14 (03) : 284 - 293
  • [10] ACIDIC FIBROBLAST GROWTH FACTOR-LIKE IMMUNOREACTIVITY IN ALZHEIMERS-DISEASE BRAIN-TISSUE
    TOOYAMA, I
    AKIYAMA, H
    MCGEER, PL
    HARA, Y
    YASUHARA, O
    KIMURA, H
    NEUROBIOLOGY OF AGING, 1990, 11 (03) : 288 - 289