Takenouchi Takato, Iwamaru Yoshifumi, Imamura Morikazu, Kato Nobuko, Sugama Shuei, Fujita Masayo, Hashimoto Makoto, Sato Mitsuru, Okada Hiroyuki, Yokoyama Takashi, Mohri Shirou, Kitani Hiroshi
Transgenic Animal Research Center, National Institute of Agrobiological Sciences, Ohwashi 1-2, Tsukuba, Ibaraki 305-8634, Japan.
FEBS Lett. 2007 Jun 26;581(16):3019-26. doi: 10.1016/j.febslet.2007.05.057. Epub 2007 May 29.
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.
我们最近建立了持续感染鼠适应型瘙痒病ME7(ScMG20/ME7)的小鼠小胶质细胞,用于朊病毒发病机制的体外研究。在此,我们发现ScMG20/ME7细胞对P2X7受体激动剂高度敏感,表现为持续的Ca(2+)内流、膜孔形成、细胞死亡和白细胞介素-1β释放。P2X7 mRNA表达在这些细胞中以及在瘙痒病感染的小鼠脑中均上调。用戊聚糖多硫酸盐处理可消除ScMG20/ME7细胞培养物中朊病毒蛋白的传染性和疾病相关形式,然而,P2X7受体的高敏感性仍然存在。这些结果表明,朊病毒感染可能强烈影响小鼠小胶质细胞中的P2X7受体系统。