Hyperphosphorylation and aggregation of tau in mice expressing normal human tau isoforms

被引:564
作者
Andorfer, C
Kress, Y
Espinoza, M
de Silva, R
Tucker, KL
Barde, YA
Duff, K
Davies, P
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 10461 USA
[3] UCL, Reta Lila Weston Inst Neurol Studies, London, England
[4] Friedrich Miescher Inst, CH-4002 Basel, Switzerland
[5] Nathan S Kline Inst Psychiat Res, Ctr Dementia Res, Orangeburg, NY USA
关键词
aggregation; Alzheimer's disease; non-mutant tau; phosphorylation; transgenic;
D O I
10.1046/j.1471-4159.2003.01879.x
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
Neurofibrillary tangles are composed of insoluble aggregates of the microtubule-associated protein tau. In Alzheimer's disease the accumulation of neurofibrillary tangles occurs in the absence of tau mutations. Here we present mice that develop pathology from non-mutant human tau, in the absence of other exogenous factors, including beta-amyloid. The pathology in these mice is Alzheimer-like, with hyperphosphorylated tau accumulating as aggregated paired helical filaments. This pathologic tau accumulates in the cell bodies and dendrites of neurons in a spatiotemporally relevant distribution.
引用
收藏
页码:582 / 590
页数:9
相关论文
共 45 条
[1]   PKA phosphorylations on tau: Developmental studies in the mouse [J].
Andorfer, CA ;
Davies, P .
DEVELOPMENTAL NEUROSCIENCE, 2000, 22 (04) :303-309
[2]   Tau protein isoforms, phosphorylation and role in neurodegenerative disorders [J].
Buée, L ;
Bussière, T ;
Buée-Scherrer, V ;
Delacourte, A ;
Hof, PR .
BRAIN RESEARCH REVIEWS, 2000, 33 (01) :95-130
[3]  
Buée L, 1999, BRAIN PATHOL, V9, P681
[4]   Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylation [J].
Dayanandan, R ;
Van Slegtenhorst, M ;
Mack, TGA ;
Ko, L ;
Yen, SH ;
Leroy, K ;
Brion, JP ;
Anderton, BH ;
Hutton, M ;
Lovestone, S .
FEBS LETTERS, 1999, 446 (2-3) :228-232
[5]   Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies [J].
de Silva, R ;
Lashley, T ;
Gibb, G ;
Hanger, D ;
Hope, A ;
Reid, A ;
Bandopadhyay, R ;
Utton, M ;
Strand, C ;
Jowett, T ;
Khan, N ;
Anderton, B ;
Wood, N ;
Holton, J ;
Revesz, T ;
Lees, A .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2003, 29 (03) :288-302
[6]   Characterization of pathology in transgenic mice over-expressing human genomic and cDNA tau transgenes [J].
Duff, K ;
Knight, H ;
Refolo, LM ;
Sanders, S ;
Yu, X ;
Picciano, M ;
Malester, B ;
Hutton, M ;
Adamson, J ;
Goedert, M ;
Burki, K ;
Davies, P .
NEUROBIOLOGY OF DISEASE, 2000, 7 (02) :87-98
[7]   CLONING AND SEQUENCING OF THE CDNA-ENCODING AN ISOFORM OF MICROTUBULE-ASSOCIATED PROTEIN TAU CONTAINING 4 TANDEM REPEATS - DIFFERENTIAL EXPRESSION OF TAU PROTEIN MESSENGER-RNAS IN HUMAN-BRAIN [J].
GOEDERT, M ;
SPILLANTINI, MG ;
POTIER, MC ;
ULRICH, J ;
CROWTHER, RA .
EMBO JOURNAL, 1989, 8 (02) :393-399
[8]   MULTIPLE ISOFORMS OF HUMAN MICROTUBULE-ASSOCIATED PROTEIN-TAU - SEQUENCES AND LOCALIZATION IN NEUROFIBRILLARY TANGLES OF ALZHEIMERS-DISEASE [J].
GOEDERT, M ;
SPILLANTINI, MG ;
JAKES, R ;
RUTHERFORD, D ;
CROWTHER, RA .
NEURON, 1989, 3 (04) :519-526
[9]   Structural and functional differences between 3-repeat and 4-repeat tau isoforms - Implications for normal tau function and the onset of neurodegenerative disease [J].
Goode, BL ;
Chau, M ;
Denis, PE ;
Feinstein, SC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (49) :38182-38189
[10]   Tau and transgenic animal models [J].
Götz, J .
BRAIN RESEARCH REVIEWS, 2001, 35 (03) :266-286