| Literature DB >> 17544414 |
Takato Takenouchi1, Yoshifumi Iwamaru, Morikazu Imamura, Nobuko Kato, Shuei Sugama, Masayo Fujita, Makoto Hashimoto, Mitsuru Sato, Hiroyuki Okada, Takashi Yokoyama, Shirou Mohri, Hiroshi Kitani.
Abstract
We recently established mouse microglial cells persistently infected with mouse-adapted scrapie ME7 (ScMG20/ME7) for in vitro study of prion pathogenesis. Here, we found that ScMG20/ME7 cells were hypersensitive to P2X7 receptor agonists, as demonstrated by sustained Ca(2+) influx, membrane pore formation, cell death, and interleukin-1beta release. P2X7 mRNA expression was upregulated in these cells, and also in scrapie-infected mice brains. Treatment with pentosan polysulfate eliminated the infectivity and disease-related forms of prion protein from ScMG20/ME7 cell cultures, however, hypersensitivity of P2X7 receptors remained. These results suggest that prion infections may strongly affect the P2X7 receptor system in mouse microglial cells.Entities:
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Year: 2007 PMID: 17544414 DOI: 10.1016/j.febslet.2007.05.057
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124