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Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein.

Nature genetics | Aug 28, 2000

http://www.ncbi.nlm.nih.gov/pubmed/10932182

Neurofibrillary tangles (NFT) composed of the microtubule-associated protein tau are prominent in Alzheimer disease (AD), Pick disease, progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD). Mutations in the gene (Mtapt) encoding tau protein cause frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17), thereby proving that tau dysfunction can directly result in neurodegeneration. Expression of human tau containing the most common FTDP-17 mutation (P301L) results in motor and behavioural deficits in transgenic mice, with age- and gene-dose-dependent development of NFT. This phenotype occurred as early as 6.5 months in hemizygous and 4.5 months in homozygous animals. NFT and Pick-body-like neuronal lesions occurred in the amygdala, septal nuclei, pre-optic nuclei, hypothalamus, midbrain, pons, medulla, deep cerebellar nuclei and spinal cord, with tau-immunoreactive pre-tangles in the cortex, hippocampus and basal ganglia. Areas with the most NFT had reactive gliosis. Spinal cord had axonal spheroids, anterior horn cell loss and axonal degeneration in anterior spinal roots. We also saw peripheral neuropathy and skeletal muscle with neurogenic atrophy. Brain and spinal cord contained insoluble tau that co-migrated with insoluble tau from AD and FTDP-17 brains. The phenotype of mice expressing P301L mutant tau mimics features of human tauopathies and provides a model for investigating the pathogenesis of diseases with NFT.

Pubmed ID: 10932182 RIS Download

Mesh terms: Amino Acid Substitution | Animals | Brachial Plexus Neuritis | Brain Stem | Cell Count | Gene Expression | Mice | Mice, Inbred C57BL | Mice, Inbred DBA | Mice, Transgenic | Movement Disorders | Muscle, Skeletal | Mutation | Neurofibrillary Tangles | Neurons | Spinal Cord | tau Proteins

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Associated grants

  • Agency: PHS HHS, Id: P01
  • Agency: PHS HHS, Id: R01

Mouse Genome Informatics (Data, Gene Annotation)

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