Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein.

Details

Serval ID
serval:BIB_1A06DA63C104
Type
Article: article from journal or magazin.
Collection
Publications
Title
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein.
Journal
Nature
Author(s)
Büeler H., Fischer M., Lang Y., Bluethmann H., Lipp H.P., DeArmond S.J., Prusiner S.B., Aguet M., Weissmann C.
ISSN
0028-0836 (Print)
ISSN-L
0028-0836
Publication state
Published
Issued date
1992
Volume
356
Number
6370
Pages
577-582
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
Publication Status: ppublish
Abstract
PrPC is a host protein anchored to the outer surface of neurons and to a lesser extent of lymphocytes and other cells. The transmissible agent (prion) responsible for scrapie is believed to be a modified form of PrPC. Mice homozygous for disrupted PrP genes have been generated. Surprisingly, they develop and behave normally for at least seven months, and no immunological defects are apparent. It is now feasible to determine whether mice devoid of PrPC can propagate prions and are susceptible to scrapie pathogenesis.
Keywords
Aging, Animals, Base Sequence, Blastocyst/physiology, Blotting, Northern, Blotting, Western, Brain/growth & development, Brain/physiology, Cell Membrane/physiology, Crosses, Genetic, Female, Heterozygote Detection, Male, Membrane Proteins/genetics, Mice, Molecular Sequence Data, Neurons/physiology, Oligodeoxyribonucleotides, Polymerase Chain Reaction, PrPSc Proteins, Pregnancy, Prions/genetics, RNA/genetics, RNA/isolation & purification, Recombination, Genetic, Restriction Mapping, Scrapie/genetics, Stem Cells/physiology
Pubmed
Web of science
Create date
28/01/2008 12:37
Last modification date
20/08/2019 13:51
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