Cerebrospinal fluid tissue transglutaminase as a biochemical marker for Alzheimer's disease

被引:46
作者
Bonelli, RM
Aschoff, A
Niederwieser, G
Heuberger, C
Jirikowski, G
机构
[1] Hosp BHB Eggenberg, Dept Neurol & Psychiat, A-8021 Graz, Austria
[2] Univ Jena, Dept Anat 2, D-07740 Jena, Germany
[3] Graz Univ Technol, Dept Math, A-8010 Graz, Austria
关键词
Alzheimer's disease; tissue transglutaminase; apoptosis; vascular dementia; tau protein;
D O I
10.1006/nbdi.2002.0535
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tissue transglutaminase (tTG) is an indicator of acute cell death in vitro. An increase in tTG protein level is found in postmortem Alzheimer's disease (AD) brains as well as in Huntington's disease. No study revealed tTG in vivo so far. We investigated the concentrations of tTG in the cerebrospinal fluid (CSF) obtained from 84 patients using ELISA assays. We compared 33 patients with probable AD to 18 patients with probable vascular dementia (VaD) and 33 control patients without neuropsychological deficit. Diagnosis was supported by CSF parameter and neuroimaging. We found a highly significant difference (P = 0.001) between the concentration of tTG in the AD groups (7.58 pg/ml) and controls (2.99 pg/ml). There was no statistical difference between controls and VaD (2.93 pg/ml). Interestingly, tTG did not show an association with tau protein, Abeta42, apoE4, neuropsychological items, or age. Males showed lower tTG values than females; however, this difference did not reach statistical significance. To our knowledge, this is the first demonstration that tTG is increased in AD in vivo. Our results suggest that tTG may be a powerful biochemical marker of the acute degenerating process in vivo. It may serve as completion of CSF analysis in the diagnosis of dementing disorders and may be a simple way of assessing the efficacy of possible new antiapoptotic drugs. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:106 / 110
页数:5
相关论文
共 38 条
[1]   DNA damage and apoptosis in Alzheimer's disease: Colocalization with c-Jun immunoreactivity, relationship to brain area, and effect of postmortem delay [J].
Anderson, AJ ;
Su, JH ;
Cotman, CW .
JOURNAL OF NEUROSCIENCE, 1996, 16 (05) :1710-1719
[2]   RAPID AND TRANSIENT ALTERATIONS IN TRANSGLUTAMINASE ACTIVITY IN RAT SUPERIOR CERVICAL-GANGLIA FOLLOWING DENERVATION OR AXOTOMY [J].
ANDO, M ;
KUNII, S ;
TATEMATSU, T ;
NAGATA, Y .
NEUROSCIENCE RESEARCH, 1993, 17 (01) :47-52
[3]   Evaluation of CSF-tau and CSF-Aβ42 as diagnostic markers for Alzheimer disease in clinical practice [J].
Andreasen, N ;
Minthon, L ;
Davidsson, P ;
Vanmechelen, E ;
Vanderstichele, H ;
Winblad, B ;
Blennow, K .
ARCHIVES OF NEUROLOGY, 2001, 58 (03) :373-379
[4]   Tissue transglutaminase selectively modifies proteins associated with truncated mutant huntingtin in intact cells [J].
Chun, WJ ;
Lesort, M ;
Tucholski, J ;
Faber, PW ;
MacDonald, ME ;
Ross, CA ;
Johnson, GVW .
NEUROBIOLOGY OF DISEASE, 2001, 8 (03) :391-404
[5]   Tissue transglutaminase does not contribute to the formation of mutant Huntingtin aggregates [J].
Chun, WJ ;
Lesort, M ;
Tucholski, J ;
Ross, CA ;
Johnson, GVW .
JOURNAL OF CELL BIOLOGY, 2001, 153 (01) :25-34
[6]  
CITRON BA, 2000, J BIOL CHEM, V29, P29
[7]   A POTENTIAL ROLE FOR APOPTOSIS IN NEURODEGENERATION AND ALZHEIMERS-DISEASE [J].
COTMAN, CW ;
ANDERSON, AJ .
MOLECULAR NEUROBIOLOGY, 1995, 10 (01) :19-45
[8]   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
[9]   TRANSGLUTAMINASE CATALYZES THE FORMATION OF SODIUM DODECYL SULFATE-INSOLUBLE, ALZ-50-REACTIVE POLYMERS OF TAU [J].
DUDEK, SM ;
JOHNSON, GVW .
JOURNAL OF NEUROCHEMISTRY, 1993, 61 (03) :1159-1162
[10]   CELL-CYCLE KINETICS, TISSUE TRANSGLUTAMINASE AND PROGRAMMED CELL-DEATH (APOPTOSIS) [J].
ELALAOUI, S ;
MIAN, S ;
LAWRY, J ;
QUASH, G ;
GRIFFIN, M .
FEBS LETTERS, 1992, 311 (02) :174-178