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经鼠类库鲁病斑块证实的克雅氏病阳性传播。

Positive transmission of Creutzfeldt-Jakob disease verified by murine kuru plaques.

作者信息

Kitamoto T, Tateishi J, Sawa H, Doh-Ura K

机构信息

Department of Neuropathology, Kyushu University, Fukuoka, Japan.

出版信息

Lab Invest. 1989 Apr;60(4):507-12.

PMID:2468821
Abstract

Kuru plaque is a pathognomonic feature in the brain of patients with Creutzfeldt-Jakob disease (CJD) and in the brain of CJD-infected mice. Kuru plaques from CJD-infected mice were immunolabeled with rabbit anti-murine prion protein (PrP) absorbed with human PrP, but not so with mouse anti-human PrP. Therefore, the murine kuru plaque is composed of the host (mouse) PrP and can be distinguished antigenically from human PrP. Immunostaining using the anti-murine PrP and formic acid enhancement on tissue sections revealed not only birefringent kuru plaques but also nonbirefringent diffuse and small PrP accumulations. This immunohistochemical detection of kuru plaques provides more positive evidence than heretofore employed histochemical approaches. There were kuru plaques in brains of the first passage mice inoculated with tissues from 30 (91%) of 33 patients with CJD, the 3 negative patients belonging to a type of Gerstmann-Sträussler syndrome. Tissues from 6 other demented patients did not produce kuru plaques. In the evaluation of spongiform changes, mice inoculated with tissues from 23 (70%) of 33 patients were considered cases of successful transmission. In some mice, kuru plaques were present in the absence of spongiform changes. Further inoculations from 9 mice with kuru plaques but no spongiform changes were successful in almost all mice. Therefore, mice with murine kuru plaques in the absence of spongiform changes are also infectious. Thus, the presence of murine-specific kuru plaques can serve as another hallmark of a successful transmission.

摘要

库鲁氏斑是克雅氏病(CJD)患者大脑以及感染CJD的小鼠大脑中的特征性病变。用经人朊蛋白吸附的兔抗鼠朊蛋白(PrP)对感染CJD小鼠的库鲁氏斑进行免疫标记,但用鼠抗人PrP则无法标记。因此,鼠源库鲁氏斑由宿主(小鼠)PrP组成,在抗原性上可与人PrP区分开来。使用抗鼠PrP进行免疫染色并在组织切片上进行甲酸增强处理,不仅揭示了双折射的库鲁氏斑,还发现了非双折射的弥漫性和小的PrP聚集物。这种对库鲁氏斑的免疫组织化学检测比以往采用的组织化学方法提供了更多阳性证据。接种33例CJD患者中30例(91%)的组织的第一代传代小鼠大脑中有库鲁氏斑,3例阴性患者属于格斯特曼-施特劳斯勒综合征类型。其他6例痴呆患者的组织未产生库鲁氏斑。在评估海绵状病变时,接种33例患者中23例(70%)的组织的小鼠被认为是成功传播的病例。在一些小鼠中,没有海绵状病变时也存在库鲁氏斑。对9只只有库鲁氏斑而无海绵状病变的小鼠进行进一步传代,几乎所有小鼠都成功了。因此,没有海绵状病变但有鼠源库鲁氏斑的小鼠也具有传染性。因此,鼠特异性库鲁氏斑的存在可作为成功传播的另一个标志。

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