IMMUNOHISTOCHEMICAL AND IMMUNOELECTRON MICROSCOPIC CHARACTERIZATION OF CEREBROVASCULAR AND SENILE PLAQUE AMYLOID IN AGED DOGS BRAINS

被引:45
作者
ISHIHARA, T
GONDO, T
TAKAHASHI, M
UCHINO, F
IKEDA, SI
ALLSOP, D
IMAI, K
机构
[1] QUEENS UNIV BELFAST,SCH BIOL & BIOCHEM,DIV BIOCHEM,BELFAST BT7 1NN,ANTRIM,NORTH IRELAND
[2] SAPPORO MED COLL,DEPT INTERNAL MED,SECT 1,SAPPORO,HOKKAIDO 060,JAPAN
[3] SHINSHU UNIV,DEPT MED NEUROL,MATSUMOTO,NAGANO 390,JAPAN
关键词
AMYLOID; BETA/A4; PROTEIN; CEREBROVASCULAR AMYLOID; DIFFUSE PLAQUE; AGED DOG; IMMUNOELECTRON MICROSCOPY;
D O I
10.1016/0006-8993(91)91122-H
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Immunohistochemical and immunoelectron microscopical studies were carried out on 28 aged dogs' brains. Amyloid deposits were seen in the arteries and capillaries in the leptomeninges and in superificial areas of the cortices in 19 (67.9%) of the 28 dogs (10-22 years of age). Immunohistochemically, these amyloid deposits were reactive for anti-beta/A4 antibody. Additionally, a variable number of parenchymal deposits with diffuse beta/A4-immunoreactivity (diffuse plaques) was also noted throughout the cerebral cortex in 24/28 dogs (85.7%). However, these plaque lesions were undetectable in Congo red staining. Electron microscopically, amyloid fibrils, measuring 10 nm in width, were located mainly in the tunica media of the arteries, and in less involved vessels they tended to be present among collagen fibres in the adventitia and smooth muscle cells in the outer layer of the media. The plaque lesions appeared to contain sparse aggregations of amyloid fibrils. In immunoelectron microscopical examinations, all amyloid fibrils in both blood vessels and plaques were selectively labelled by gold particles. These findings indicate that aged dogs can provide a useful experimental model for research into the beta/A4-type of cerebral amyloidosis commonly seen in Alzheimer's disease.
引用
收藏
页码:196 / 205
页数:10
相关论文
共 48 条
[2]   EARLY SENILE PLAQUES IN DOWNS-SYNDROME BRAINS SHOW A CLOSE RELATIONSHIP WITH CELL-BODIES OF NEURONS [J].
ALLSOP, D ;
HAGA, SI ;
HAGA, C ;
IKEDA, SI ;
MANN, DMA ;
ISHII, T .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1989, 15 (06) :531-542
[3]   MONOCLONAL-ANTIBODIES RAISED AGAINST A SUBSEQUENCE OF SENILE PLAQUE CORE PROTEIN REACT WITH PLAQUE CORES, PLAQUE PERIPHERY AND CEREBROVASCULAR AMYLOID IN ALZHEIMERS-DISEASE [J].
ALLSOP, D ;
LANDON, M ;
KIDD, M ;
LOWE, JS ;
REYNOLDS, GP ;
GARDNER, A .
NEUROSCIENCE LETTERS, 1986, 68 (02) :252-256
[4]  
ALLSOP D, 1990, AM J PATHOL, V136, P255
[5]   LOCALIZATION OF AMYLOID BETA-PROTEIN MESSENGER-RNA IN BRAINS FROM PATIENTS WITH ALZHEIMERS-DISEASE [J].
BAHMANYAR, S ;
HIGGINS, GA ;
GOLDGABER, D ;
LEWIS, DA ;
MORRISON, JH ;
WILSON, MC ;
SHANKAR, SK ;
GAJDUSEK, DC .
SCIENCE, 1987, 237 (4810) :77-80
[6]   ULTRASTRUCTURAL-LOCALIZATION OF ANTIGENIC SITES ON OSMIUM-FIXED TISSUES APPLYING THE PROTEIN A-GOLD TECHNIQUE [J].
BENDAYAN, M ;
ZOLLINGER, M .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1983, 31 (01) :101-109
[7]  
CASTANO EM, 1988, LAB INVEST, V58, P122
[8]  
CORIA F, 1987, AM J PATHOL, V129, P422
[9]   NEUROFIBRILLARY TANGLES AND SENILE PLAQUES IN AGED BEARS [J].
CORK, LC ;
POWERS, RE ;
SELKOE, DJ ;
DAVIES, P ;
GEYER, JJ ;
PRICE, DL .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1988, 47 (06) :629-641
[10]   CEREBRAL AMYLOID ANGIOPATHY [J].
COSGROVE, GR ;
LEBLANC, R ;
MEAGHERVILLEMURE, K ;
ETHIER, R .
NEUROLOGY, 1985, 35 (05) :625-631