Korth Carsten, Kaneko Kiyotoshi, Groth Darlene, Heye Norbert, Telling Glenn, Mastrianni James, Parchi Piero, Gambetti Pierluigi, Will Robert, Ironside James, Heinrich Cornelia, Tremblay Patrick, DeArmond Stephen J, Prusiner Stanley B
Institute for Neurodegenerative Diseases and Department of Neurology, University of California, San Francisco, CA 94143, USA.
Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4784-9. doi: 10.1073/pnas.2627989100. Epub 2003 Apr 8.
Transgenic (Tg) mouse lines that express chimeric mouse-human prion protein (PrP), designated MHu2M, are susceptible to prions from patients with sporadic Creutzfeldt-Jakob disease (sCJD). With the aim of decreasing the incubation time to fewer than 200 days, we constructed transgenes in which one or more of the nine human residues in MHu2M were changed to mouse. The construct with murine residues at positions 165 and 167 was expressed in Tg(MHu2M,M165V,E167Q) mice and resulted in shortening the incubation time to approximately 110 days for prions from sCJD patients. The construct with a murine residue at position 96 resulted in lengthening the incubation time to more than 280 days for sCJD prions. When murine residues 96, 165, and 167 were expressed, the abbreviated incubation times for sCJD prions were abolished. Variant CJD prions showed prolonged incubation times between 300 and 700 days in Tg(MHu2M) mice on first passage and incubation times of approximately 350 days in Tg(MHu2M,M165V,E167Q) mice. On second and third passages of variant CJD prions in Tg(MHu2M) mice, multiple strains of prions were detected based on incubation times and the sizes of the protease-resistant, deglycosylated PrP(Sc) fragments. Our discovery of a previously undescribed chimeric transgene with abbreviated incubation times for sCJD prions should facilitate studies on the prion species barrier and human prion diversity.
表达嵌合型小鼠 - 人朊病毒蛋白(PrP)(命名为MHu2M)的转基因(Tg)小鼠品系对散发性克雅氏病(sCJD)患者的朊病毒敏感。为了将潜伏期缩短至200天以内,我们构建了转基因,其中MHu2M中的九个人类残基中的一个或多个被替换为小鼠残基。在Tg(MHu2M,M165V,E167Q)小鼠中表达在第165和167位带有鼠源残基的构建体,使得sCJD患者的朊病毒潜伏期缩短至约110天。在第96位带有鼠源残基的构建体导致sCJD朊病毒的潜伏期延长至超过280天。当表达第96、165和167位的鼠源残基时,sCJD朊病毒缩短的潜伏期消失。变异型CJD朊病毒在Tg(MHu2M)小鼠首次传代时的潜伏期延长至300至700天之间,在Tg(MHu2M,M165V,E167Q)小鼠中的潜伏期约为350天。在Tg(MHu2M)小鼠中对变异型CJD朊病毒进行第二次和第三次传代时,根据潜伏期以及蛋白酶抗性、去糖基化PrP(Sc)片段的大小检测到多种朊病毒株。我们发现了一种以前未描述的嵌合转基因,其对sCJD朊病毒具有缩短的潜伏期,这应该有助于对朊病毒种间屏障和人类朊病毒多样性的研究。