• 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

MNZTASi001-A的产生,这是一种源自原发性进行性多发性硬化症患者的人多能干细胞系。

Generation of MNZTASi001-A, a human pluripotent stem cell line from a person with primary progressive multiple sclerosis.

作者信息

Mehta Ashish, Lu Peter, Taylor Bruce V, Charlesworth Jac, Cook Anthony L, Burdon Kathryn P, Hewitt Alex W, Young Kaylene M

机构信息

Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.

Wicking Dementia Research and Education Centre, University of Tasmania, Hobart, Australia.

出版信息

Stem Cell Res. 2021 Dec;57:102568. doi: 10.1016/j.scr.2021.102568. Epub 2021 Oct 12.

DOI:10.1016/j.scr.2021.102568
PMID:34678664
Abstract

Multiple sclerosis (MS) is a chronic autoimmune and neurodegenerative disease that results in immune cell infiltration of the central nervous system (CNS) and demyelination in young adults. Substantial progress has been made in developing disease modifying therapies for people with relapsing-remitting MS, but options remain limited for people with primary progressive MS (PPMS). PPMS accounts for ∼15% of MS diagnoses. Herein, we generated a human induced pluripotent stem cell line (hiPSC) from a person with clinically definite PPMS. This disease-specific hiPSC line will be useful for studying PPMS in vitro, allowing the generation of immune and CNS cell types.

摘要

多发性硬化症(MS)是一种慢性自身免疫性神经退行性疾病,会导致免疫细胞浸润中枢神经系统(CNS)并在年轻人中引发脱髓鞘。在为复发缓解型MS患者开发疾病修正疗法方面已取得了重大进展,但对于原发性进展型MS(PPMS)患者而言,治疗选择仍然有限。PPMS约占MS诊断病例的15%。在此,我们从一名临床确诊为PPMS的患者身上生成了一种人诱导多能干细胞系(hiPSC)。这种疾病特异性hiPSC系将有助于在体外研究PPMS,从而能够生成免疫细胞和CNS细胞类型。

相似文献

1
Generation of MNZTASi001-A, a human pluripotent stem cell line from a person with primary progressive multiple sclerosis.MNZTASi001-A的产生,这是一种源自原发性进行性多发性硬化症患者的人多能干细胞系。
Stem Cell Res. 2021 Dec;57:102568. doi: 10.1016/j.scr.2021.102568. Epub 2021 Oct 12.
2
Generation of RRMS and PPMS specific iPSCs as a platform for modeling Multiple Sclerosis.生成 RRMS 和 PPMS 特异性 iPSCs 作为多发性硬化症建模的平台。
Stem Cell Res. 2021 May;53:102319. doi: 10.1016/j.scr.2021.102319. Epub 2021 Apr 15.
3
Transcriptional abnormalities in induced pluripotent stem cell-derived oligodendrocytes of individuals with primary progressive multiple sclerosis.原发性进行性多发性硬化症患者诱导多能干细胞来源的少突胶质细胞中的转录异常。
Front Cell Neurosci. 2022 Sep 28;16:972144. doi: 10.3389/fncel.2022.972144. eCollection 2022.
4
Translocator Protein Ligand PIGA1138 Reduces Disease Symptoms and Severity in Experimental Autoimmune Encephalomyelitis Model of Primary Progressive Multiple Sclerosis.转位蛋白配体 PIGA1138 可减轻原发性进行性多发性硬化实验性自身免疫性脑脊髓炎模型的疾病症状和严重程度。
Mol Neurobiol. 2022 Mar;59(3):1744-1765. doi: 10.1007/s12035-022-02737-2. Epub 2022 Jan 11.
5
Genetic differences between primary progressive and relapsing-remitting multiple sclerosis: The impact of immune-related genes variability.原发性进行性和复发缓解型多发性硬化症之间的遗传差异:免疫相关基因变异性的影响。
Mult Scler Relat Disord. 2019 Apr;29:130-136. doi: 10.1016/j.msard.2019.01.033. Epub 2019 Jan 24.
6
Disease-Modifying Treatment in Progressive Multiple Sclerosis.进展性多发性硬化症的疾病修正治疗
Curr Treat Options Neurol. 2018 Apr 7;20(5):12. doi: 10.1007/s11940-018-0496-3.
7
Serious infections in patients with relapsing and progressive forms of multiple sclerosis: A German claims data study.复发型和进展型多发性硬化症患者的严重感染:一项德国索赔数据研究。
Mult Scler Relat Disord. 2022 Dec;68:104245. doi: 10.1016/j.msard.2022.104245. Epub 2022 Oct 17.
8
A comparison of serum inflammatory parameters in progressive forms of multiple sclerosis.多发性硬化进行性形式的血清炎症参数比较。
Mult Scler Relat Disord. 2023 Nov;79:105004. doi: 10.1016/j.msard.2023.105004. Epub 2023 Sep 11.
9
Generation and characterisation of four multiple sclerosis iPSC lines from a single family.从一个家族中产生并鉴定出四个多发性硬化症 iPSC 系。
Stem Cell Res. 2022 Jul;62:102828. doi: 10.1016/j.scr.2022.102828. Epub 2022 Jun 5.
10
CXCL10 and CXCL13 chemokines in patients with relapsing remitting and primary progressive multiple sclerosis.CXCL10 和 CXCL13 趋化因子在复发缓解型和原发性进展型多发性硬化症患者中的作用。
J Neurol Sci. 2017 Sep 15;380:22-26. doi: 10.1016/j.jns.2017.06.048. Epub 2017 Jun 30.

引用本文的文献

1
From Molecules to Models: miRNAs and Advanced Human Platforms of Neurodegeneration and Repair in Multiple Sclerosis.从分子到模型:微小RNA与多发性硬化症神经退行性变和修复的先进人类平台
Int J Mol Sci. 2025 Sep 8;26(17):8740. doi: 10.3390/ijms26178740.
2
Brain organoid methodologies to explore mechanisms of disease in progressive multiple sclerosis.用于探索进展性多发性硬化症疾病机制的脑类器官方法
Front Cell Neurosci. 2024 Dec 18;18:1488691. doi: 10.3389/fncel.2024.1488691. eCollection 2024.
3
Research progress of autoimmune diseases based on induced pluripotent stem cells.
基于诱导多能干细胞的自身免疫性疾病研究进展。
Front Immunol. 2024 Apr 24;15:1349138. doi: 10.3389/fimmu.2024.1349138. eCollection 2024.
4
Induced pluripotent stem cell derived pericytes respond to mediators of proliferation and contractility.诱导多能干细胞衍生的周细胞对增殖和收缩的介质有反应。
Stem Cell Res Ther. 2024 Mar 3;15(1):59. doi: 10.1186/s13287-024-03671-x.