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Journal of Virology, February 2007, p. 1524-1527, Vol. 81, No. 3
0022-538X/07/$08.00+0 doi:10.1128/JVI.01379-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Research Center for Prion Diseases, National Institute of Animal Health, Kannondai 3-1-5, Tsukuba, Ibaraki 305-8602,1 Transgenic Animal Research Center, National Institute of Agrobiological Sciences, Ohwashi 1-2, Tsukuba, Ibaraki 305-8634,2 Nippi Research Institute of Biomatrix, Senjyu-Midroricho 1-1-1, Adachi, Tokyo 120-8601, Japan3
Received 30 June 2006/ Accepted 14 November 2006
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.
Published ahead of print on 22 November 2006.
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