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Tauopathy with paired helical filaments in an aged chimpanzee.

The Journal of comparative neurology | 2008

An enigmatic feature of age-related neurodegenerative diseases is that they seldom, if ever, are fully manifested in nonhuman species under natural conditions. The neurodegenerative tauopathies are typified by the intracellular aggregation of hyperphosphorylated microtubule-associated protein tau (MAPT) and the dysfunction and death of affected neurons. We document the first case of tauopathy with paired helical filaments in an aged chimpanzee (Pan troglodytes). Pathologic forms of tau in neuronal somata, neuropil threads, and plaque-like clusters of neurites were histologically identified throughout the neocortex and, to a lesser degree, in allocortical and subcortical structures. Ultrastructurally, the neurofibrillary tangles consisted of tau-immunoreactive paired helical filaments with a diameter and helical periodicity indistinguishable from those seen in Alzheimer's disease. A moderate degree of Abeta deposition was present in the cerebral vasculature and, less frequently, in senile plaques. Sequencing of the exons and flanking intronic regions in the genomic MAPT locus disclosed no mutations that are associated with the known human hereditary tauopathies, nor any polymorphisms of obvious functional significance. Although the lesion profile in this chimpanzee differed somewhat from that in Alzheimer's disease, the copresence of paired helical filaments and Abeta-amyloidosis indicates that the molecular mechanisms for the pathogenesis of the two canonical Alzheimer lesions--neurofibrillary tangles and senile plaques--are present in aged chimpanzees.

Pubmed ID: 18481275 RIS Download

Associated grants

  • Agency: NIA NIH HHS, United States
    Id: P01AG026423
  • Agency: NCRR NIH HHS, United States
    Id: P51 RR000165-477541
  • Agency: NCRR NIH HHS, United States
    Id: P51 RR000165
  • Agency: NIA NIH HHS, United States
    Id: P01 AG026423-02
  • Agency: NIA NIH HHS, United States
    Id: P50 AG025688
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS045879
  • Agency: NIA NIH HHS, United States
    Id: P50AG025688
  • Agency: NIA NIH HHS, United States
    Id: P01 AG026423
  • Agency: NCRR NIH HHS, United States
    Id: RR-00165

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