BETA-AMYLOID PROTEIN-PRECURSOR AND TAU MESSENGER-RNA LEVELS VERSUS BETA-AMYLOID PLAQUE AND NEUROFIBRILLARY TANGLES IN THE AGED HUMAN BRAIN

被引:27
作者
OYAMA, F
SHIMADA, H
OYAMA, R
TITANI, K
IHARA, Y
机构
[1] UNIV TOKYO,FAC MED,INST BRAIN RES,DEPT NEUROPATHOL,7-3-1 HONGO,BUNKYO KU,TOKYO 113,JAPAN
[2] TOKYO METROPOLITAN GERIATR HOSP & INST GERONTOL,DEPT PATHOL,TOKYO,JAPAN
[3] FUJITA HLTH UNIV,SCH MED,INST COMPREHENS MED SCI,DIV BIOMED POLYMER SCI,TOYOAKE,AICHI,JAPAN
[4] TOKYO MED COLL,DEPT PATHOL,TOKYO 160,JAPAN
[5] TOKYO METROPOLITAN GERIATR HOSP & INST GERONTOL,DEPT NEUROPHYSIOL,TOKYO,JAPAN
[6] TOKYO METROPOLITAN GERIATR HOSP & INST GERONTOL,INST GERONTOL,TOKYO 173,JAPAN
关键词
ALZHEIMERS DISEASE; AGED BRAIN; BETA-AMYLOID PROTEIN PRECURSOR MESSENGER RNA LEVEL; TAU MESSENGER RNA LEVEL; ISOFORM;
D O I
10.1111/j.1471-4159.1993.tb13388.x
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
To learn whether or not the levels of beta-amyloid protein precursor (APP) and tau mRNAs are related to the formation of beta-amyloid and neurofibrillary tangles, we quantified these mRNA levels in three cortical regions of 38 aged human brains, which were examined immunocytochemically for beta-amyloid and tangles. Marked individual variabilities were noted in APP and tau mRNA levels among elderly individuals. The mean APP mRNA level was slightly reduced in the beta-amyloid plaque (+ +) group, but not in the plaque (+) group, compared to the plaque (-) group. Some brains in the plaque (-) group showed increased APP expression, the extent of which was not seen in the plaque (+) or (+ +) group. The differences in the mean tau mRNA levels were not statistically significant among the tangle (-), (+), and (+ +) groups. These results show that beta-protein and tau deposition do not accompany increased expression of the APP and tau genes, respectively, and thus suggest that factors other than gene expression may be at work in the progression of beta-amyloid and/or tangle formation in the aged human brain.
引用
收藏
页码:1658 / 1664
页数:7
相关论文
共 57 条
[1]   IMAGING PLATE ILLUMINATES MANY FIELDS [J].
AMEMIYA, Y ;
MIYAHARA, J .
NATURE, 1988, 336 (6194) :89-90
[2]  
ANDERSON JM, 1983, J NEUROL SCI, V58, P233
[3]   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
[4]  
BARTON AJL, 1990, AM J PATHOL, V137, P497
[5]   SIZING AND MAPPING OF EARLY ADENOVIRUS MESSENGER-RNAS BY GEL-ELECTROPHORESIS OF S1 ENDONUCLEASE-DIGESTED HYBRIDS [J].
BERK, AJ ;
SHARP, PA .
CELL, 1977, 12 (03) :721-732
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P456
[7]  
CLARK A, 1989, CELL TISSUE RES, V257, P179
[8]   PURIFICATION AND CHARACTERIZATION OF A PEPTIDE FROM AMYLOID-RICH PANCREASES OF TYPE-2 DIABETIC-PATIENTS [J].
COOPER, GJS ;
WILLIS, AC ;
CLARK, A ;
TURNER, RC ;
SIM, RB ;
REID, KBM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (23) :8628-8632
[9]   THE EFFECT OF AGE AND ALZHEIMERS-DISEASE ON PYRAMIDAL NEURON DENSITY IN THE INDIVIDUAL FIELDS OF THE HIPPOCAMPAL-FORMATION [J].
DAVIES, DC ;
HORWOOD, N ;
ISAACS, SL ;
MANN, DMA .
ACTA NEUROPATHOLOGICA, 1992, 83 (05) :510-517
[10]  
DEBEER FC, 1982, LANCET, V2, P231