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Prion Diseases pp 103-112 | Cite as

A transgenic model of a familial prion disease

  • D. A. Harris
  • R. Chiesa
  • B. Drisaldi
  • E. Quaglio
  • A. Migheli
  • P. Piccardo
  • B. Ghetti
Chapter
Part of the Archives of Virology. Supplementa book series (ARCHIVES SUPPL, volume 16)

Summary

We have generated lines of transgenic mice that express a mutant prion protein containing 14 octapeptide repeats whose human homologue is associated with an inherited prion dementia. These mice develop an ataxic illness that begins at 65 days of age when the transgene array is homozygous, and results in death by 115–138 days. Starting from birth, mutant PrP is converted into a protease-resistant and detergent-insoluble form that resembles PrPSc, and this form accumulates dramatically in many brain regions throughout the lifetime of the mice. As PrP accumulates, there is massive apoptosis of cerebellar granule cells, as well as astrocytosis and deposition of PrP in a punctate pattern. These results establish a new transgenic animal model of an inherited human prion disease, and provide important insights into the molecular pathogenesis of these disorders.

Keywords

Prion Protein Prion Disease Cerebellar Granule Cell Fatal Familial Insomnia Human Prion Disease 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Wien 2000

Authors and Affiliations

  • D. A. Harris
    • 1
  • R. Chiesa
    • 1
  • B. Drisaldi
    • 1
  • E. Quaglio
    • 1
  • A. Migheli
    • 2
  • P. Piccardo
    • 3
  • B. Ghetti
    • 3
  1. 1.Department of Cell Biology and PhysiologyWashington University School of MedicineSt. LouisUSA
  2. 2.Laboratory of Neuropathology, Department of NeuroscienceUniversity of TurinTurinItaly
  3. 3.Division of NeuropathologyIndiana University School of MedicineIndianapolisUSA

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