Arima Kazuhiko, Nishida Noriyuki, Sakaguchi Suehiro, Shigematsu Kazuto, Atarashi Ryuichiro, Yamaguchi Naohiro, Yoshikawa Daisuke, Yoon Jaewoo, Watanabe Ken, Kobayashi Nobuyuki, Mouillet-Richard Sophie, Lehmann Sylvain, Katamine Shigeru
Department of Molecular Microbiology and Immunology, Nagasaki University Graduate School of Biomedical Sciences, Sakamoto 1-12-4, Nagasaki 852-8523, Japan.
J Virol. 2005 Jun;79(11):7104-12. doi: 10.1128/JVI.79.11.7104-7112.2005.
Abnormal prion protein (PrP(Sc)) plays a central role in the transmission of prion diseases, but the molecular basis of prion strains with distinct biological characteristics remains to be elucidated. We analyzed the characteristics of prion disease by using mice inoculated with the Chandler and Fukuoka-1 strains propagated in a cultured mouse neuronal cell line, GT1-7, which is highly permissive to replication of the infectious agents. Strain-specific biological characteristics, including clinical manifestations, incubation period as related to the infectious unit, and pathological profiles, remained unchanged after passages in the cell cultures. We noted some differences in the biochemical aspects of PrP(Sc) between brain tissues and GT1-7 cells which were unlikely to affect the strain phenotypes. On the other hand, the proteinase K-resistant PrP core fragments derived from Fukuoka-1-infected tissues and cells were slightly larger than those from Chandler-infected versions. Moreover, Fukuoka-1 infection, but not Chandler infection, gave an extra fragment with a low molecular weight, approximately 13 kDa, in both brain tissues and GT1-7 cells. This cell culture model persistently infected with different strains will provide a new insight into the understanding of the molecular basis of prion diversity.
异常朊病毒蛋白(PrP(Sc))在朊病毒疾病传播中起核心作用,但具有不同生物学特性的朊病毒株的分子基础仍有待阐明。我们通过使用接种了在培养的小鼠神经元细胞系GT1-7中传代的钱德勒(Chandler)株和福冈-1(Fukuoka-1)株的小鼠来分析朊病毒疾病的特征,GT1-7细胞系对感染性因子的复制具有高度易感性。在细胞培养中传代后,包括临床表现、与感染单位相关的潜伏期和病理特征在内的毒株特异性生物学特性保持不变。我们注意到脑组织和GT1-7细胞之间PrP(Sc)的生化方面存在一些差异,这些差异不太可能影响毒株表型。另一方面,源自福冈-1感染组织和细胞的蛋白酶K抗性PrP核心片段略大于源自钱德勒感染样本的片段。此外,福冈-1感染而非钱德勒感染在脑组织和GT1-7细胞中都产生了一个额外的低分子量片段,约为13 kDa。这种持续感染不同毒株的细胞培养模型将为理解朊病毒多样性的分子基础提供新的见解。