• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

皮质基底节变性和核上性麻痹中的嗜银丝状结构。

Argyrophilic thread-like structure in corticobasal degeneration and supranuclear palsy.

作者信息

Ikeda K, Akiyama H, Haga C, Kondo H, Arima K, Oda T

机构信息

Department of Neuropathology, Tokyo Institute of Psychiatry, Japan.

出版信息

Neurosci Lett. 1994 Jun 20;174(2):157-9. doi: 10.1016/0304-3940(94)90010-8.

DOI:10.1016/0304-3940(94)90010-8
PMID:7526285
Abstract

Massive argyrophilic thread-like structures (ATS) are observed in corticobasal degeneration and, in varied degrees, in some cases of progressive supranuclear palsy. Immunohistochemically, ATS has a full length of phosphorylated tau epitopes without ubiquitin. Gallyas- and immuno-electron microscopic observation revealed that ATS is a cytoskeletal abnormality occurred in both the inner and outer loop of the oligodendroglia. tau-Positive oligodendroglial tangles were distributed in the same region as ATS.

摘要

在皮质基底节变性中观察到大量嗜银丝状结构(ATS),在某些进行性核上性麻痹病例中也不同程度地观察到。免疫组织化学显示,ATS全长具有磷酸化tau表位,无泛素。加利亚斯染色和免疫电子显微镜观察显示,ATS是少突胶质细胞内环和外环均出现的细胞骨架异常。tau阳性的少突胶质细胞缠结分布在与ATS相同的区域。

相似文献

1
Argyrophilic thread-like structure in corticobasal degeneration and supranuclear palsy.皮质基底节变性和核上性麻痹中的嗜银丝状结构。
Neurosci Lett. 1994 Jun 20;174(2):157-9. doi: 10.1016/0304-3940(94)90010-8.
2
Corticobasal degeneration: widespread argentophilic threads and glia in addition to neurofibrillary tangles. Similarities of cytoskeletal abnormalities in corticobasal degeneration and progressive supranuclear palsy.皮质基底节变性:除神经原纤维缠结外,还存在广泛的嗜银细丝和胶质细胞。皮质基底节变性与进行性核上性麻痹细胞骨架异常的相似性。
J Neurol Sci. 1996 Jun;138(1-2):66-77. doi: 10.1016/0022-510x(95)00347-5.
3
Corticobasal degeneration: a disease with widespread appearance of abnormal tau and neurofibrillary tangles, and its relation to progressive supranuclear palsy.皮质基底节变性:一种广泛出现异常tau蛋白和神经原纤维缠结的疾病及其与进行性核上性麻痹的关系。
Acta Neuropathol. 1994;88(2):113-21. doi: 10.1007/BF00294503.
4
[Neuropathology of corticobasal degeneration].[皮质基底节变性的神经病理学]
No To Shinkei. 1996 Jun;48(6):521-32.
5
Intracellular processing of aggregated tau differs between corticobasal degeneration and progressive supranuclear palsy.在皮质基底节变性和进行性核上性麻痹中,聚集tau蛋白的细胞内加工过程存在差异。
Neuroreport. 2001 Apr 17;12(5):935-8. doi: 10.1097/00001756-200104170-00014.
6
Corticobasal degeneration presenting with progressive spasticity.
Neurology. 2007 Mar 6;68(10):791-2. doi: 10.1212/01.wnl.0000256729.99951.44.
7
Ultrastructural characterization of the tau-immunoreactive tubules in the oligodendroglial perikarya and their inner loop processes in progressive supranuclear palsy.
Acta Neuropathol. 1997 Jun;93(6):558-66. doi: 10.1007/s004010050652.
8
Does corticobasal degeneration exist? A clinicopathological re-evaluation.皮质基底节变性是否存在?临床病理再评估。
Brain. 2010 Jul;133(Pt 7):2045-57. doi: 10.1093/brain/awq123.
9
[Glial abnormalities in progressive supranuclear palsy and corticobasal degeneration].[进行性核上性麻痹和皮质基底节变性中的胶质细胞异常]
Zhonghua Bing Li Xue Za Zhi. 2004 Apr;33(2):125-9.
10
Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: tau pathologies with exclusively "exon 10" isoforms.进行性核上性麻痹和皮质基底节变性中的神经原纤维变性:仅含“第10外显子”异构体的tau蛋白病变
J Neurochem. 1999 Mar;72(3):1243-9. doi: 10.1046/j.1471-4159.1999.0721243.x.

引用本文的文献

1
Spread of pathological human Tau from neurons to oligodendrocytes and loss of high-firing pyramidal neurons in aging mice.病理性人 Tau 从神经元向少突胶质细胞的传播以及衰老小鼠中高放电锥体神经元的丢失。
Cell Rep. 2022 Nov 15;41(7):111646. doi: 10.1016/j.celrep.2022.111646.
2
Tau Isoform-Driven CBD Pathology Transmission in Oligodendrocytes in Humanized Tau Mice.人源化tau小鼠少突胶质细胞中tau异构体驱动的CBD病理传播
Front Neurol. 2021 Jan 15;11:589471. doi: 10.3389/fneur.2020.589471. eCollection 2020.
3
Cellular Biology of Tau Diversity and Pathogenic Conformers.
Tau多样性与致病构象体的细胞生物学
Front Neurol. 2020 Nov 12;11:590199. doi: 10.3389/fneur.2020.590199. eCollection 2020.
4
Tau and Axonal Transport Misregulation in Tauopathies.tau 蛋白和轴突运输失调在 tau 病中的作用。
Adv Exp Med Biol. 2019;1184:81-95. doi: 10.1007/978-981-32-9358-8_7.
5
Axonal Degeneration in Tauopathies: Disease Relevance and Underlying Mechanisms.tau蛋白病中的轴突退化:疾病相关性及潜在机制
Front Neurosci. 2017 Oct 17;11:572. doi: 10.3389/fnins.2017.00572. eCollection 2017.
6
Pathology of Neurodegenerative Diseases.神经退行性疾病的病理学
Cold Spring Harb Perspect Biol. 2017 Jul 5;9(7):a028035. doi: 10.1101/cshperspect.a028035.
7
Filamentous aggregations of phosphorylated α-synuclein in Schwann cells (Schwann cell cytoplasmic inclusions) in multiple system atrophy.多发性系统萎缩中 Schwann 细胞(施旺细胞质包涵体)内磷酸化的α-突触核蛋白丝聚集物。
Acta Neuropathol Commun. 2015 May 21;3:29. doi: 10.1186/s40478-015-0208-0.
8
Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.进行性核上性麻痹全基因组关联的常见变异和表达数量性状位点评估。
Neurobiol Aging. 2014 Jun;35(6):1514.e1-12. doi: 10.1016/j.neurobiolaging.2014.01.010. Epub 2014 Jan 13.
9
Transgenic mouse model of tau pathology in astrocytes leading to nervous system degeneration.星形胶质细胞中tau病理导致神经系统退化的转基因小鼠模型。
J Neurosci. 2005 Apr 6;25(14):3539-50. doi: 10.1523/JNEUROSCI.0081-05.2005.
10
Biochemical analysis of tau proteins in argyrophilic grain disease, Alzheimer's disease, and Pick's disease : a comparative study.嗜银颗粒病、阿尔茨海默病和皮克病中tau蛋白的生化分析:一项比较研究。
Am J Pathol. 2002 Oct;161(4):1135-41. doi: 10.1016/s0002-9440(10)64390-8.