| Literature DB >> 17121794 |
Yoshifumi Iwamaru1, Takato Takenouchi, Kazumasa Ogihara, Megumi Hoshino, Masuhiro Takata, Morikazu Imamura, Yuichi Tagawa, Hiroko Hayashi-Kato, Yuko Ushiki-Kaku, Yoshihisa Shimizu, Hiroyuki Okada, Morikazu Shinagawa, Hiroshi Kitani, Takashi Yokoyama.
Abstract
Several lines of evidence suggest that microglia have important roles in the pathogenesis of prion diseases. Here, we establish a novel microglial cell line (MG20) from neonatal tga20 mice that overexpress murine prion protein. After exposure to Chandler scrapie, we observed the replication and accumulation of disease-associated forms of the prion protein in MG20 cells up to the 15th passage. Furthermore, MG20 cells were susceptible to ME7, Obihiro scrapie, and bovine spongiform encephalopathy agents. Thus, MG20 cell lines persistently infected with various murine prion strains provide a useful model for the study of the pathogenesis of prion diseases.Entities:
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Year: 2006 PMID: 17121794 PMCID: PMC1797525 DOI: 10.1128/JVI.01379-06
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103