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免疫组化和超微结构证据表明泛神经型克雅氏病患者的白质退化发病机制:奇异星形细胞中诱导型一氧化氮合酶的过表达。

Immunohistochemical and ultrastructural evidence for the pathogenesis of white matter degeneration in patients with panencephalopathic-type Creutzfeldt-Jakob disease: Inducible nitric oxide synthase overexpression in bizarre astrocytes.

机构信息

Division of Neuropathology, Faculty of Medicine, Tottori University, Yonago, Japan.

School of Medicine, Hiroshima University, Hiroshima, Japan.

出版信息

Neuropathology. 2020 Aug;40(4):319-327. doi: 10.1111/neup.12646. Epub 2020 Apr 1.

Abstract

Excessive production of nitric oxide (NO) due to the overinduction of inducible nitric oxide synthase (iNOS) has a severe cytotoxic effect, which may relate to the pathogenesis of neurodegenerative disorders. In this study, we report the novel finding that iNOS is overinduced in a large number of bizarre astrocytes in the white matter of patients with panencephalopathic (PE)-type Creutzfeldt-Jakob disease (CJD). This study was carried out on brain tissue from seven patients with PE-type CJD. As controls, 12 normal individuals and nine patients with cerebral infarction were examined. We identified a large number of bizarre astrocytes in the degenerative cerebral white matter in PE-type CJD. Using immunohistochemistry, only bizarre astrocytes in PE-type CJD showed strong immunoreactivity for both iNOS and superoxide dismutase 1 (SOD1). Ultrastructural examination demonstrated that these bizarre astrocytes contained many free polyribosome-like granules. No significant iNOS immunoreactivity was observed in either the astrocytes of patients with cerebral infarcts or in the normal controls. This study suggests that the iNOS-overexpressing astrocytes, especially iNOS-overexpressing bizarre astrocytes, could play an important role in the development of white matter lesions in PE-type CJD. Our data also suggest that the bizarre astrocytes could be protecting themselves from the cytotoxicity of NO by producing SOD1. These immunohistochemical findings are supported by the ultrastructural observation of numerous polyribosome granules restricted to the cytoplasm of these bizarre astrocytes.

摘要

由于诱导型一氧化氮合酶(iNOS)的过度诱导,导致一氧化氮(NO)的过度产生具有严重的细胞毒性作用,这可能与神经退行性疾病的发病机制有关。在这项研究中,我们报告了一个新的发现,即在泛脑病(PE)型克雅氏病(CJD)患者的白质中大量出现奇异星形胶质细胞过度诱导 iNOS。这项研究是在 7 名 PE 型 CJD 患者的脑组织上进行的。作为对照,检查了 12 名正常个体和 9 名脑梗死患者。我们在 PE 型 CJD 的退行性脑白质中发现了大量奇异星形胶质细胞。使用免疫组织化学,只有在 PE 型 CJD 中奇异星形胶质细胞对 iNOS 和超氧化物歧化酶 1(SOD1)均表现出强烈的免疫反应性。超微结构检查表明,这些奇异星形胶质细胞含有许多游离的多核糖体样颗粒。在脑梗死患者的星形胶质细胞或正常对照中均未观察到明显的 iNOS 免疫反应性。这项研究表明,iNOS 过度表达的星形胶质细胞,特别是 iNOS 过度表达的奇异星形胶质细胞,可能在 PE 型 CJD 白质病变的发展中发挥重要作用。我们的数据还表明,奇异星形胶质细胞可能通过产生 SOD1 来保护自己免受 NO 的细胞毒性。这些免疫组织化学发现得到了超微结构观察的支持,即在这些奇异星形胶质细胞的细胞质中观察到许多多核糖体颗粒。

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