| Literature DB >> 20193663 |
Kan Luo1, Shu Li, Min Xie, Di Wu, WenXi Wang, Rui Chen, Liqin Huang, Tao Huang, Daiwen Pang, Gengfu Xiao.
Abstract
Prion diseases are fatal neurodegenerative disorders resulting from structural conversion of the cellular isoform of PrP(C) to the infectious scrapie isoform PrP(Sc). It is believed that such structural alteration may occur within the internalization pathway. However, there is no direct evidence to support this hypothesis. Employing quantum dots (QDs) as a probe, we have recorded a real-time movie demonstrating the process of prion internalization in a living cell for the first time. The entire internalization process can be divided into four discrete but connected stages. In addition, using methyl-beta-cyclodextrin to disrupt cell membrane cholesterol, we show that lipid rafts play an important role in locating cellular PrP(C) to the cell membrane and in initiating PrP(C) endocytosis. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20193663 DOI: 10.1016/j.bbrc.2010.02.159
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575