Granules in glial cells of patients with Alzheimer's disease are immunopositive for C-terminal sequences of beta-amyloid protein

被引:67
作者
Akiyama, H [1 ]
Schwab, C [1 ]
Kondo, H [1 ]
Mori, H [1 ]
Kametani, F [1 ]
Ikeda, K [1 ]
McGeer, PL [1 ]
机构
[1] UNIV BRITISH COLUMBIA,KINSMEN LAB NEUROL RES,VANCOUVER,BC V6T 1W5,CANADA
关键词
beta-amyloid protein (A beta); microglia; astrocytes; phagocytosis; proteolysis; immunohistochemistry;
D O I
10.1016/S0304-3940(96)12474-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Granular structures that are recognized by antibodies specific for the C-terminal but not the N-terminal sequences of the beta-amyloid protein (A beta) fragments are present in a subset of microglia and astrocytes in Alzheimer brain tissue. The immunohistochemical profile indicates that the A beta in these granules is truncated between the residues 17 and 31 and terminates at the residue 42 or 43, Such granule-containing glia occur only in brain areas with the heavy A beta deposits. Whether the intraglial A beta fragments accumulate as a result of phagocytosis of extracellular A beta or are formed intracellularly by glial cells from amyloid precursor protein (APP) remains unknown.
引用
收藏
页码:169 / 172
页数:4
相关论文
共 13 条
[1]   BRAIN MICROGLIA CONSTITUTIVELY EXPRESS BETA-2 INTEGRINS [J].
AKIYAMA, H ;
MCGEER, PL .
JOURNAL OF NEUROIMMUNOLOGY, 1990, 30 (01) :81-93
[2]  
FRACKOWIAK J, 1992, ACTA NEUROPATHOL, V84, P225
[3]  
GOWING E, 1994, J BIOL CHEM, V269, P10987
[4]   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) [J].
IWATSUBO, T ;
ODAKA, A ;
SUZUKI, N ;
MIZUSAWA, H ;
NUKINA, N ;
IHARA, Y .
NEURON, 1994, 13 (01) :45-53
[5]   INFORMATION-PROCESSING WITHIN THE MOTOR CORTEX .2. INTRACORTICAL CONNECTIONS BETWEEN NEURONS RECEIVING SOMATOSENSORY CORTICAL INPUT AND MOTOR OUTPUT NEURONS OF THE CORTEX [J].
KANEKO, T ;
CARIA, MA ;
ASANUMA, H .
JOURNAL OF COMPARATIVE NEUROLOGY, 1994, 345 (02) :172-184
[6]   EARLY AMYLOID-BETA DEPOSITS SHOW DIFFERENT IMMUNOREACTIVITY TO THE AMINO-TERMINAL AND CARBOXY-TERMINAL REGIONS OF BETA-PEPTIDE IN ALZHEIMERS-DISEASE AND DOWNS-SYNDROME BRAIN [J].
KIDA, E ;
WISNIEWSKI, KE ;
WISNIEWSKI, HM .
NEUROSCIENCE LETTERS, 1995, 193 (02) :105-108
[7]   INTRACELLULAR ACCUMULATION AND RESISTANCE TO DEGRADATION OF THE ALZHEIMER AMYLOID A4/BETA-PROTEIN [J].
KNAUER, MF ;
SOREGHAN, B ;
BURDICK, D ;
KOSMOSKI, J ;
GLABE, CG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (16) :7437-7441
[8]   MICROGLIA IN DEGENERATIVE NEUROLOGICAL DISEASE [J].
MCGEER, PL ;
KAWAMATA, T ;
WALKER, DG ;
AKIYAMA, H ;
TOOYAMA, I ;
MCGEER, EG .
GLIA, 1993, 7 (01) :84-92
[9]  
MORI H, 1992, J BIOL CHEM, V267, P17082
[10]   BETA-AMYLOID PEPTIDE PRODUCED IN-VITRO IS DEGRADED BY PROTEINASES RELEASED BY CULTURED-CELLS [J].
NAIDU, A ;
QUON, D ;
CORDELL, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (03) :1369-1374