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Showing papers by "Ryuichiro Atarashi published in 2004"


DOI
28 Oct 2004
TL;DR: It is indicated that PrPLP/Dpl have no potential to undergo pathogenic conversion to form a prion-like infectious particle.
Abstract: Cellular prion protein, PrP C , undergoes pathogenic structural conversion into the proteinase K (PK)-resistant isoform, PrP Sc , to constitute a nucleic acid-free infectious agent, so called a prion. To determine whether a recently identified PrP-like protein, named PrPLP/Dpl, could also be transformed to a prion-like protein, we intracerebrally inoculated a mouse-adapted Fukuoka-1 prion into Ngsk and Zrch I mice either homozygously (Prnp 0/0 ) or heterozygously (Prnp 0/+ ) devoid of PrP C . Only the former expressed PrPLP/Dpl ectopically in the brains, particularly in neurons. Ngsk Prnp 0/+ and Zrch I Prnp 0/+ mice similarly developed the disease. The diseased Ngsk Prnp 0/+ mice transmitted the disease to the mice expressing PrP C but not to the mice expressing PrPLP/Dpl, showing abundant accumulation of PrP Sc but not PK-resistant PrPLP/Dpl in the brains. Moreover, the inoculated Ngsk Prnp 0/0 mice neither developed the disease nor produced any infectivity transmissible to PrPLP/Dpl-expressing mice. These results indicate that PrPLP/Dpl have no potential to undergo pathogenic conversion to form a prion-like infectious particle.

1 citations