Publication Date:
2001-08-25
Description:
JNPL3 transgenic mice expressing a mutant tau protein, which develop neurofibrillary tangles and progressive motor disturbance, were crossed with Tg2576 transgenic mice expressing mutant beta-amyloid precursor protein (APP), thus modulating the APP-Abeta (beta-amyloid peptide) environment. The resulting double mutant (tau/APP) progeny and the Tg2576 parental strain developed Abeta deposits at the same age; however, relative to JNPL3 mice, the double mutants exhibited neurofibrillary tangle pathology that was substantially enhanced in the limbic system and olfactory cortex. These results indicate that either APP or Abeta influences the formation of neurofibrillary tangles. The interaction between Abeta and tau pathologies in these mice supports the hypothesis that a similar interaction occurs in Alzheimer's disease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lewis, J -- Dickson, D W -- Lin, W L -- Chisholm, L -- Corral, A -- Jones, G -- Yen, S H -- Sahara, N -- Skipper, L -- Yager, D -- Eckman, C -- Hardy, J -- Hutton, M -- McGowan, E -- New York, N.Y. -- Science. 2001 Aug 24;293(5534):1487-91.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Birdsall Building, Mayo Clinic Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11520987" target="_blank"〉PubMed〈/a〉
Keywords:
Alzheimer Disease/genetics/metabolism/*pathology
;
Amyloid beta-Peptides/*metabolism
;
Amyloid beta-Protein Precursor/genetics/*metabolism
;
Animals
;
Brain/metabolism/*pathology
;
Crosses, Genetic
;
Disease Models, Animal
;
Female
;
Limbic System/metabolism/pathology
;
Male
;
Mice
;
Mice, Transgenic
;
Mutation
;
Nerve Degeneration
;
Neurofibrillary Tangles/genetics/metabolism/*pathology
;
Neurons/ultrastructure
;
Peptide Fragments/metabolism
;
Plaque, Amyloid/genetics/metabolism/*pathology
;
RNA, Messenger/genetics/metabolism
;
Sex Characteristics
;
Solubility
;
Spinal Cord/metabolism/pathology
;
tau Proteins/genetics/*metabolism
Print ISSN:
0036-8075
Electronic ISSN:
1095-9203
Topics:
Biology
,
Chemistry and Pharmacology
,
Computer Science
,
Medicine
,
Natural Sciences in General
,
Physics
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