ELEVATION OF MICROTUBULE-ASSOCIATED PROTEIN TAN IN THE CEREBROSPINAL-FLUID OF PATIENTS WITH ALZHEIMERS-DISEASE

被引:195
作者
VIGOPELFREY, C
SEUBERT, P
BARBOUR, R
BLOMQUIST, C
LEE, M
LEE, D
CORIA, F
CHANG, L
MILLER, B
LIEBERBURG, I
SCHENK, D
机构
[1] ATHENA NEUROSCI INC,S SAN FRANCISCO,CA 94080
[2] SEGOVIA GEN HOSP,DEPT NEUROL,SEGOVIA,SPAIN
[3] UNIV CALIF LOS ANGELES,HARBOR MED CTR,DEPT NEUROL,TORRANCE,CA 90509
关键词
D O I
10.1212/WNL.45.4.788
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Currently, there is no biochemical marker clinically available to test for the presence of Alzheimer's disease (AD). Recent studies suggest that the core component of AD-associated neurofibrillary tangles (NFTs), the microtubule-associated protein tau, might be present in CSF. This study focuses on establishing both the presence of tau in CSF and its potential utility in the diagnosis of AD. We obtained CSF from 181 individuals; 71 of these were diagnosed as having probable AD by NINCDS-ADRDA criteria. The remaining 110 individuals were divided into three groups: (1) age-matched demented non-AD patients (n = 25), (2) neurologic controls (n = 59), and (3) other controls (n = 26). We developed a sensitive enzyme-linked immunosorbent tau assay using monoclonal antibodies prepared against recombinant human tau. We confirmed specificity of the antibodies by a combination of immunoprecipitation and immunoblot results. By this assay we measured that the AD population has a mean level of tau 50% greater than the non-AD dementia patients. Comparing AD patients with all other groups, the difference in tau levels as analyzed by one-way ANOVA is highly statistically significant (p < 0.001). Postmortem analysis of two AD patients with high levels of CSF tau revealed a high density of NFTs in the hippocampus. There was no significant correlation between tau and age in the non-AD groups. This study suggests that CSF tau is elevated in AD and might be a useful aid in antemortem diagnosis.
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页码:788 / 793
页数:6
相关论文
共 18 条
[1]  
BRION JP, 1985, ARCH BIOL, V96, P229
[2]  
CHELEY S, 1992, J CELL SCI, V102, P739
[3]   ALZHEIMERS-DISEASE - TAU PROTEINS, THE PROMOTING FACTORS OF MICROTUBULE ASSEMBLY, ARE MAJOR COMPONENTS OF PAIRED HELICAL FILAMENTS [J].
DELACOURTE, A ;
DEFOSSEZ, A .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1986, 76 (2-3) :173-186
[4]   BIOCHEMICAL ASSAY OF ALZHEIMERS-DISEASE ASSOCIATED PROTEIN(S) IN HUMAN BRAIN-TISSUE - A CLINICAL-STUDY [J].
GHANBARI, HA ;
MILLER, BE ;
HAIGLER, HJ ;
ARATO, M ;
BISSETTE, G ;
DAVIES, P ;
NEMEROFF, CB ;
PERRY, EK ;
PERRY, R ;
RAVID, R ;
SWAAB, DF ;
WHETSELL, WO ;
ZEMLAN, FP .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1990, 263 (21) :2907-2910
[5]  
GRUNDKEIQBAL I, 1986, J BIOL CHEM, V261, P6084
[6]   PLAQUE-ONLY ALZHEIMER-DISEASE IS USUALLY THE LEWY BODY VARIANT, AND VICE-VERSA [J].
HANSEN, LA ;
MASLIAH, E ;
GALASKO, D ;
TERRY, RD .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1993, 52 (06) :648-654
[7]   BRAIN LEVELS OF MICROTUBULE-ASSOCIATED PROTEIN-TAU ARE ELEVATED IN ALZHEIMERS-DISEASE - A RADIOIMMUNO-SLOT-BLOT ASSAY FOR NANOGRAMS OF THE PROTEIN [J].
KHATOON, S ;
GRUNDKEIQBAL, I ;
IQBAL, K .
JOURNAL OF NEUROCHEMISTRY, 1992, 59 (02) :750-753
[8]   OVEREXPRESSION OF TAU IN A NONNEURONAL CELL INDUCES LONG CELLULAR PROCESSES [J].
KNOPS, J ;
KOSIK, KS ;
LEE, G ;
PARDEE, JD ;
COHENGOULD, L ;
MCCONLOGUE, L .
JOURNAL OF CELL BIOLOGY, 1991, 114 (04) :725-733
[9]   CONTINUOUS CULTURES OF FUSED CELLS SECRETING ANTIBODY OF PREDEFINED SPECIFICITY [J].
KOHLER, G ;
MILSTEIN, C .
NATURE, 1975, 256 (5517) :495-497
[10]   EPITOPES THAT SPAN THE TAU-MOLECULE ARE SHARED WITH PAIRED HELICAL FILAMENTS [J].
KOSIK, KS ;
ORECCHIO, LD ;
BINDER, L ;
TROJANOWSKI, JQ ;
LEE, VMY ;
LEE, G .
NEURON, 1988, 1 (09) :817-825