Variable deposition of amyloid beta-protein (A beta) with the carboxy-terminus that ends at residue valine(40) (A beta 40) in the cerebral cortex of patients with Alzheimer's disease: A double-labeling immunohistochemical study with antibodies specific for A beta 40 and the A beta that ends at residues alanine(42)/threonine(43) (A beta 42)

被引:30
作者
Akiyama, H
Mori, H
Sahara, N
Kondo, H
Ikeda, K
Nishimura, T
Oda, T
McGeer, PL
机构
[1] SHIMOFUSA SANAT,NATL HOSP,CHIBA 266,JAPAN
[2] UNIV BRITISH COLUMBIA,KINSMEN LAB NEUROL RES,VANCOUVER,BC V6T 1W5,CANADA
关键词
diffuse deposits; amyloid angiopathy; senile plaques;
D O I
10.1023/A:1021910729963
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
Amyloid beta-protein (A beta) deposits in the cerebral cortices of patients with Alzheimer's disease (AD) were investigated immunohistochemically to determine their carboxy terminal sequences. Antibodies specific for A beta terminating at residue valine(40) (A beta 40) and at residues alanine(42)/threonine(43) (A beta 42) were used. Virtually all parenchymal A beta deposits were positive for A beta 42. Many of these deposits were also partially or completely labeled for A beta 40. The degree of A beta 40 labeling varied from area to area within a given brain and from AD case to AD case. In contrast to parenchymal deposits, A beta 40 labeled essentially all the vascular deposits which constitute amyloid angiopathy (AA), with A beta 42 occurring variably in some of these deposits. Occasional AA was found, however, in which A beta 42 predominated or was exclusively deposited. Such a diversity of A beta species, both in brain parenchyma and in AA, suggests that multiple C-terminal processing mechanisms occur in the cell types responsible for these deposits.
引用
收藏
页码:1499 / 1506
页数:8
相关论文
共 26 条
  • [1] BRAIN MICROGLIA CONSTITUTIVELY EXPRESS BETA-2 INTEGRINS
    AKIYAMA, H
    MCGEER, PL
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1990, 30 (01) : 81 - 93
  • [2] Cummings BJ, 1996, NEUROBIOL AGING, V17, P653
  • [3] Fukumoto H, 1996, AM J PATHOL, V148, P259
  • [4] REGIONAL VARIATION IN THE DISTRIBUTION OF APOLIPOPROTEIN-E AND A-BETA IN ALZHEIMERS-DISEASE
    GEARING, M
    SCHNEIDER, JA
    ROBINS, RS
    HOLLISTER, RD
    MORI, H
    GAMES, D
    HYMAN, BT
    MIRRA, SS
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1995, 54 (06) : 833 - 841
  • [5] GEARING M, 1997, IN PRESS NEUROBIOL A
  • [6] Giaccone G, 1996, AM J PATHOL, V148, P79
  • [7] GOWING E, 1994, J BIOL CHEM, V269, P10987
  • [8] AMYLOID-BETA PROTEIN (A-BETA) IN ALZHEIMERS-DISEASE BRAIN - BIOCHEMICAL AND IMMUNOCYTOCHEMICAL ANALYSIS WITH ANTIBODIES SPECIFIC FOR FORMS ENDING AT A-BETA-40 OR A-BETA-42(43)
    GRAVINA, SA
    HO, LB
    ECKMAN, CB
    LONG, KE
    OTVOS, L
    YOUNKIN, LH
    SUZUKI, N
    YOUNKIN, SG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (13) : 7013 - 7016
  • [9] THE COOH-TERMINUS OF THE ALZHEIMER AMYLOID A-BETA PEPTIDE - DIFFERENCES IN LENGTH INFLUENCE THE PROCESS OF AMYLOID DEPOSITION IN ALZHEIMER BRAIN, AND TELL US SOMETHING ABOUT RELATIONSHIPS AMONG PARENCHYMAL AND VESSEL-ASSOCIATED AMYLOID DEPOSITS
    GREENBERG, BD
    [J]. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 1995, 2 (03): : 195 - 203
  • [10] VISUALIZATION OF A-BETA-42(43) AND A-BETA-40 IN SENILE PLAQUES WITH END-SPECIFIC A-BETA MONOCLONALS - EVIDENCE THAT AN INITIALLY DEPOSITED SPECIES IS A-BETA-42(43)
    IWATSUBO, T
    ODAKA, A
    SUZUKI, N
    MIZUSAWA, H
    NUKINA, N
    IHARA, Y
    [J]. NEURON, 1994, 13 (01) : 45 - 53