• 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

运动神经元病中前角神经元内由泛素免疫细胞化学定位所定义的丝状包涵体。

A filamentous inclusion body within anterior horn neurones in motor neurone disease defined by immunocytochemical localisation of ubiquitin.

作者信息

Lowe J, Lennox G, Jefferson D, Morrell K, McQuire D, Gray T, Landon M, Doherty F J, Mayer R J

机构信息

Department of Pathology, Nottingham University Medical School, Queens Medical Centre, U.K.

出版信息

Neurosci Lett. 1988 Nov 22;94(1-2):203-10. doi: 10.1016/0304-3940(88)90296-0.

DOI:10.1016/0304-3940(88)90296-0
PMID:2853853
Abstract

Using an immunocytochemical method to localise antibodies to ubiquitin, filamentous inclusion bodies were seen in spinal anterior horn neurones in cases of motor neurone disease (MND) but not in any control cases. These inclusion bodies appeared to be closely associated with classical Bunina bodies and immuno-electron microscopy suggested that they were based on arrays of straight 10-15 nm filaments together with some granular material. These observations link the protein ubiquitin with a chronic neurodegenerative disease and extend previous observations of a close association between filamentous inclusion bodies and ubiquitin. Ubiquitin-filament inclusions should be regarded as a new hallmark in the histological diagnosis of MND.

摘要

运用免疫细胞化学方法对泛素抗体进行定位,在运动神经元病(MND)患者的脊髓前角神经元中发现了丝状包涵体,而在任何对照病例中均未发现。这些包涵体似乎与典型的布宁纳小体密切相关,免疫电子显微镜显示它们基于10 - 15纳米的直丝阵列以及一些颗粒物质。这些观察结果将蛋白质泛素与一种慢性神经退行性疾病联系起来,并扩展了先前关于丝状包涵体与泛素密切关联的观察。泛素丝包涵体应被视为MND组织学诊断中的一个新标志。

相似文献

1
A filamentous inclusion body within anterior horn neurones in motor neurone disease defined by immunocytochemical localisation of ubiquitin.运动神经元病中前角神经元内由泛素免疫细胞化学定位所定义的丝状包涵体。
Neurosci Lett. 1988 Nov 22;94(1-2):203-10. doi: 10.1016/0304-3940(88)90296-0.
2
Inclusion bodies in motor cortex and brainstem of patients with motor neurone disease are detected by immunocytochemical localisation of ubiquitin.通过泛素的免疫细胞化学定位检测运动神经元疾病患者运动皮层和脑干中的包涵体。
Neurosci Lett. 1989 Oct 23;105(1-2):7-13. doi: 10.1016/0304-3940(89)90003-7.
3
Ubiquitin deposits in anterior horn cells in motor neurone disease.运动神经元病中前角细胞内的泛素沉积。
Neurosci Lett. 1988 Nov 11;93(2-3):197-203. doi: 10.1016/0304-3940(88)90081-x.
4
Skein-like inclusions in the anterior horn cells in motor neuron disease.
J Neurol Sci. 1991 Sep;105(1):14-21. doi: 10.1016/0022-510x(91)90112-k.
5
Lewy body-like hyaline inclusions in sporadic motor neuron disease are ubiquitinated.散发性运动神经元病中的路易小体样透明包涵体发生了泛素化。
Acta Neuropathol. 1989;77(4):391-6. doi: 10.1007/BF00687373.
6
Ubiquitinated filamentous inclusions in spinal cord of patients with motor neuron disease.运动神经元病患者脊髓中的泛素化丝状包涵体。
Neurosci Lett. 1990 Jun 22;114(1):5-10. doi: 10.1016/0304-3940(90)90419-a.
7
Immunocytochemical and ultrastructural studies of lower motor neurons in amyotrophic lateral sclerosis.肌萎缩侧索硬化症中运动神经元的免疫细胞化学及超微结构研究
Ann Neurol. 1990 Feb;27(2):137-48. doi: 10.1002/ana.410270208.
8
Sporadic motor neuron disease with Lewy body-like hyaline inclusions.
Acta Neuropathol. 1989;78(5):555-60. doi: 10.1007/BF00687719.
9
Motor neuron disease/amyotrophic lateral sclerosis--lessons from ubiquitin.运动神经元病/肌萎缩侧索硬化症——来自泛素的启示
Pathol Res Pract. 1993 Sep;189(8):902-12. doi: 10.1016/S0344-0338(11)81102-7.
10
Ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis. Morphology, distribution, and specificity.
Brain. 1991 Apr;114 ( Pt 2):775-88. doi: 10.1093/brain/114.2.775.

引用本文的文献

1
Epigenetics in the formation of pathological aggregates in amyotrophic lateral sclerosis.表观遗传学在肌萎缩侧索硬化症病理聚集体形成中的作用
Front Mol Neurosci. 2024 Sep 3;17:1417961. doi: 10.3389/fnmol.2024.1417961. eCollection 2024.
2
Protein aggregation and therapeutic strategies in SOD1- and TDP-43- linked ALS.与超氧化物歧化酶1(SOD1)和TDP - 43相关的肌萎缩侧索硬化症中的蛋白质聚集及治疗策略
Front Mol Biosci. 2024 May 24;11:1383453. doi: 10.3389/fmolb.2024.1383453. eCollection 2024.
3
Nitric Oxide/Nitric Oxide Synthase System in the Pathogenesis of Neurodegenerative Disorders-An Overview.
神经退行性疾病发病机制中的一氧化氮/一氧化氮合酶系统——综述
Antioxidants (Basel). 2023 Mar 20;12(3):753. doi: 10.3390/antiox12030753.
4
Frontotemporal lobar degeneration with TAR DNA-binding protein 43 (TDP-43): its journey of more than 100 years.额颞叶变性伴 TAR DNA 结合蛋白 43(TDP-43):跨越百年的历程。
J Neurol. 2022 Aug;269(8):4030-4054. doi: 10.1007/s00415-022-11073-3. Epub 2022 Mar 23.
5
DNA damage in embryonic neural stem cell determines FTLDs' fate via early-stage neuronal necrosis.胚胎神经干细胞中的 DNA 损伤通过早期神经元坏死决定 FTLDs 的命运。
Life Sci Alliance. 2021 Jun 15;4(7). doi: 10.26508/lsa.202101022. Print 2021 Jul.
6
Upper Motor Neuron Disorders: Primary Lateral Sclerosis, Upper Motor Neuron Dominant Amyotrophic Lateral Sclerosis, and Hereditary Spastic Paraplegia.上运动神经元疾病:原发性侧索硬化症、上运动神经元为主型肌萎缩侧索硬化症和遗传性痉挛性截瘫。
Brain Sci. 2021 May 11;11(5):611. doi: 10.3390/brainsci11050611.
7
Phenotypic diversity in ALS and the role of poly-conformational protein misfolding.ALS 中的表型多样性和多构象蛋白错误折叠的作用。
Acta Neuropathol. 2021 Jul;142(1):41-55. doi: 10.1007/s00401-020-02222-x. Epub 2020 Sep 15.
8
Amyotrophic lateral sclerosis with appearance of many skein-like inclusions in anterior horn cells.肌萎缩侧索硬化症,前角细胞出现许多线团样包涵体。
Int J Clin Exp Pathol. 2019 Nov 1;12(11):4156-4161. eCollection 2019.
9
Prion-Like Propagation of Protein Misfolding and Aggregation in Amyotrophic Lateral Sclerosis.肌萎缩侧索硬化症中蛋白质错误折叠和聚集的朊病毒样传播
Front Mol Neurosci. 2019 Nov 1;12:262. doi: 10.3389/fnmol.2019.00262. eCollection 2019.
10
Using proteomics to identify ubiquitin ligase-substrate pairs: how novel methods may unveil therapeutic targets for neurodegenerative diseases.利用蛋白质组学鉴定泛素连接酶-底物对:新方法如何揭示神经退行性疾病的治疗靶点。
Cell Mol Life Sci. 2019 Jul;76(13):2499-2510. doi: 10.1007/s00018-019-03082-9. Epub 2019 Mar 27.