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PMID: 12859672 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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

Journal of neurochemistry ·Vol. 86 ·No. 3 ·2003-08-00 ·Pages 582-90

Andorfer C, Kress Y, Espinoza M, de Silva R, Tucker KL, Barde YA, Duff K, Davies P

Abstract

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.

MeSH Terms
Age Factors Alternative Splicing Alzheimer Disease/genetics,metabolism,pathology Animals Brain/metabolism,pathology Brain Chemistry Dendrites/metabolism,pathology Disease Models, Animal Humans Macromolecular Substances Mice Mice, Transgenic Neurofibrillary Tangles/chemistry,metabolism,pathology Neurons/metabolism,pathology Phosphorylation Protein Isoforms/genetics,metabolism Reverse Transcriptase Polymerase Chain Reaction tau Proteins/genetics,metabolism
Chemicals
Macromolecular Substances Protein Isoforms tau Proteins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Andorfer Cathy
Departments of Neuroscience and Pathology, Albert Einstein College of Medicine, Bronx, New York, USA.
Kress Yvonne
Espinoza Marisol
de Silva Rohan
Tucker Kerry L
Barde Yves-Alain
Duff Karen
Davies Peter
Article Info
Journal
Journal of neurochemistry
Abbr.
J Neurochem
ISSN
0022-3042
Published
2003-08-00
Pages
582-90
Language
English
Region
England
NLM ID
2985190R
Subset
IM
Grants
NIA NIH HHS · R01 AG022102 · United States
NIMH NIH HHS · MH 38623 · United States
NINDS NIH HHS · NS 07098 · United States
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