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Selective neuronal targeting in prion disease
被引:170
作者:
DeArmond, SJ
[1
]
Sánchez, H
Yehiely, F
Qiu, Y
Ninchak-Casey, A
Daggett, V
Camerino, AP
Cayetano, J
Rogers, M
Groth, D
Torchia, M
Tremblay, P
Scott, MR
Cohen, FE
Prusiner, SB
机构:
[1] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Cellular & Mol Biol, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[6] Univ Washington, Dept Med Chem, Seattle, WA 98195 USA
来源:
关键词:
D O I:
10.1016/S0896-6273(00)80424-9
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The pattern of scrapie prion protein (PrPSc) accumulation in the brain is different for each prion strain. We tested whether the PrPSc deposition pattern is influenced by the Asn-linked oligosaccharides of PrPC in transgenic mice. Deletion of the first oligosaccharide altered PrPC trafficking and prevented infection with two prion strains. Deletion of the second did not alter PrPC trafficking, permitted infection with one prion strain, and had a profound effect on the PrPSc deposition pattern. Our data raise the possibility that glycosylation can modify the conformation of PrPC. Glycosylation could affect the affinity of PrPC for a particular conformer of PrPSc, thereby determining the rate of nascent PrPSc formation and the specific patterns of PrPSc deposition.
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页码:1337 / 1348
页数:12
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