Scrapie-associated prion protein accumulates in astrocytes during scrapie infection.

Abstract:

:In the course of scrapie, a transmissible spongiform encephalopathy caused by an unconventional agent, a normal cellular protein is converted to an abnormal form that copurifies with infectivity and aggregates to form deposits of amyloid. We have used immunocytochemistry and methods that enhance detection of amyloidogenic proteins to investigate the types of cells in the central nervous system which are involved in the formation of the abnormal scrapie-associated protein. We show that this protein accumulates in astrocytes prior to the cardinal neuropathological changes in scrapie--astrogliosis, vacuolation, neuron loss, and amyloid deposition. These findings implicate the astrocyte in the formation of the scrapie isoform of the prion protein and amyloid in scrapie and suggest that this cell type might also be involved in the replication of the scrapie agent.

authors

Diedrich JF,Bendheim PE,Kim YS,Carp RI,Haase AT

doi

10.1073/pnas.88.2.375

subject

Has Abstract

pub_date

1991-01-15 00:00:00

pages

375-9

issue

2

eissn

0027-8424

issn

1091-6490

journal_volume

88

pub_type

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