Argyrophilic tau-positive twisted and non-twisted tubules in astrocytic processes in brains of Alzheimer-type dementia: an electron microscopical study

被引:12
作者
Arima, K
Izumiyama, Y
Nakamura, M
Nakayama, H
Kimura, M
Ando, S
Ikeda, K
Takahashi, K
机构
[1] Tokyo Inst Psychiat, Dept Ultrastruct & Histochem, Setagaya Ku, Tokyo 1568585, Japan
[2] Natl Ctr Hosp Mental Nervous & Muscular Disorders, Dept Psychiat, Natl Ctr Neurol & Psychiat, Kodaira, Tokyo 187, Japan
[3] Tokyo Metropolitan Neurol Hosp, Dept Neuropsychiat, Fuchu, Tokyo 183, Japan
关键词
astrocytes; Alzheimer-type dementia; electron microscopy; glial fibrillary tangles; tau protein;
D O I
10.1007/s004010050762
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This report concerns pathological astrocytic tubular structures (astrocytic tubules, As-Tbs) that coexist with glial filaments in astrocytic processes In brains with presenile-onset Alzheimer-type dementia. The formation of As-Tbs appears to be related to the duration of disease and the intensity of Alzheimer histopathology. In three cases in which the disease was of extremely long duration, As-Tbs were found in the frontal and temporal neocortices, the temporal pole and the hippocampus using electron microscopy, whereas they were not round in two cases with a long, but not extremely long. illness duration. As-Tbs were almost exclusively found in the highly devastated neuropil, and we could not find them in regions of moderate neuronal degeneration despite intensive inspection. As reported previously, some As-Tbs was seen adjacent to extracellular neurofibrillary tangles (NFTs) and in perivascular astrocytes. Our novel finding is that they can exist independently from these, in the highly devastated neuropil. Two types of As-Tbs were observed, twisted tubules with periodic constrictions at 50- to 80-nm intervals and non-twisted tubules where no constrictions were seen but which had a 15-nm fuzzy outer contour. They were positively stained by anti-human tau antibody, tin antibody that does not recognize extracellular NFTs. Thus, it is most likely that As-Tbs are not the sequestration of exextracellular NFTs, and that they are of astrocytic origin. Moreover. As-Tbs showed argyrophilia. As-Tbs appear indistinguishable from dystrophic neurites under the light microscope. The present data suggest that they may be more widely distributed in the damaged cerebral neuropil than previously thought.
引用
收藏
页码:28 / 39
页数:12
相关论文
共 25 条
[1]   CORTICONIGRAL DEGENERATION WITH NEURONAL ACHROMASIA PRESENTING WITH PRIMARY PROGRESSIVE APHASIA - ULTRASTRUCTURAL AND IMMUNOCYTOCHEMICAL STUDIES [J].
ARIMA, K ;
UESUGI, H ;
FUJITA, I ;
SAKURAI, Y ;
OYANAGI, S ;
ANDOH, S ;
IZUMIYAMA, Y ;
INOSE, T .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1994, 127 (02) :186-197
[2]   Tubular profile of the Gallyas- and tau-positive argyrophilic threads in corticobasal degeneration: An electronmicroscopic study [J].
Arima, K .
NEUROPATHOLOGY, 1996, 16 (01) :65-70
[3]  
BONDAREFF W, 1990, AM J PATHOL, V137, P711
[4]   SILVER IMPREGNATION OF ALZHEIMER NEUROFIBRILLARY CHANGES COUNTERSTAINED FOR BASOPHILIC MATERIAL AND LIPOFUSCIN PIGMENT [J].
BRAAK, H ;
BRAAK, E ;
OHM, T ;
BOHL, J .
STAIN TECHNOLOGY, 1988, 63 (04) :197-200
[5]  
Chin SSM, 1996, J NEUROPATH EXP NEUR, V55, P499
[6]   METAL-CATALYZED OXIDATION RENDERS SILVER INTENSIFICATION SELECTIVE - APPLICATIONS FOR THE HISTOCHEMISTRY OF DIAMINOBENZIDINE AND NEUROFIBRILLARY CHANGES [J].
GALLYAS, F ;
WOLFF, JR .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1986, 34 (12) :1667-1672
[7]   THE USE OF GOLD-SUBSTITUTED SILVER-INTENSIFIED DIAMINOBENZIDINE (DAB) AND NON-INTENSIFIED DAB FOR SIMULTANEOUS ELECTRON-MICROSCOPIC IMMUNOPEROXIDASE LABELING OF TYROSINE-HYDROXYLASE AND GLUTAMIC-ACID DECARBOXYLASE IMMUNOREACTIVITY IN THE RAT MEDIAL PREOPTIC AREA [J].
GORCS, TJ ;
LERANTH, C ;
MACLUSKY, NJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1986, 34 (11) :1439-1447
[8]  
IHARA Y, 1990, GERONTOLOGY, V36, P15
[9]   COEXISTENCE OF PAIRED HELICAL FILAMENTS AND GLIAL FILAMENTS IN ASTROCYTIC PROCESSES WITHIN GHOST TANGLES [J].
IKEDA, K ;
HAGA, C ;
AKIYAMA, H ;
KASE, K ;
IRITANI, S .
NEUROSCIENCE LETTERS, 1992, 148 (1-2) :126-128
[10]  
IKEDA K, 1995, ACTA NEUROPATHOL, V90, P620