• 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

NGN2、ASCL1、SOX2 和 MSI1 诱导人成纤维细胞向神经前体细胞表型转变过程中的早期转录组变化的快照:RNA-Seq 研究。

A Snapshot of Early Transcriptional Changes Accompanying the Pro-Neural Phenotype Switch by NGN2, ASCL1, SOX2, and MSI1 in Human Fibroblasts: An RNA-Seq Study.

机构信息

Federal Center for Brain and Neurotechnologies, Federal Medical and Biological Agency of Russia, 117513 Moscow, Russia.

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.

出版信息

Int J Mol Sci. 2024 Nov 18;25(22):12385. doi: 10.3390/ijms252212385.

DOI:10.3390/ijms252212385
PMID:39596450
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11594342/
Abstract

Direct pro-neural reprogramming is a conversion of differentiated somatic cells to neural cells without an intermediate pluripotency stage. It is usually achieved via ectopic expression (EE) of certain transcription factors (TFs) or other reprogramming factors (RFs). Determining the transcriptional changes (TCs) caused by particular RFs in a given cell line enables an informed approach to reprogramming initiation. Here, we characterized TCs in the human fibroblast cell line LF1 on the 5th day after EE of the single well-known pro-neural RFs NGN2, ASCL1, SOX2, and MSI1. As assessed by expression analysis of the bona fide neuronal markers nestin and beta-III tubulin, all four RFs initiated pro-neuronal phenotype conversion; analysis by RNA-seq revealed striking differences in the resulting TCs, although some pathways were overlapping. ASCL1 and SOX2 were not sufficient to induce significant pro-neural phenotype switches using our EE system. NGN2 induced TCs indicative of cell phenotype changes towards neural crest cells, neural stem cells, mature neurons, as well as radial glia, astrocytes, and oligodendrocyte precursors and their mature forms. MSI1 mainly induced a switch towards early stem-like cells, such as radial glia.

摘要

直接诱导多能性重编程是一种将分化的体细胞直接转化为神经细胞的过程,而无需经过中间的多能性阶段。通常,通过异位表达(ectopic expression,EE)某些转录因子(transcription factors,TFs)或其他重编程因子(reprogramming factors,RFs)来实现这一过程。确定特定 RF 在给定细胞系中引起的转录变化(transcriptional changes,TCs)可以为重编程的启动提供一种明智的方法。在这里,我们在 LF1 人成纤维细胞系中,在 EE 单个已知的神经前体 RFs(NGN2、ASCL1、SOX2 和 MSI1)后的第 5 天,对 TCs 进行了特征描述。通过对巢蛋白和 β-III 微管蛋白等真正神经元标志物的表达分析,这四种 RF 都启动了向神经前体细胞表型的转化;RNA-seq 分析显示,尽管一些途径存在重叠,但在产生的 TCs 中存在显著差异。在我们的 EE 系统中,ASCL1 和 SOX2 不足以诱导明显的神经前体表型转换。NGN2 诱导的 TCs 表明细胞表型向神经嵴细胞、神经干细胞、成熟神经元以及放射状胶质细胞、星形胶质细胞和少突胶质细胞前体细胞及其成熟形式转变。MSI1 主要诱导向早期干细胞样细胞(如放射状胶质细胞)的转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/02614d3f3de9/ijms-25-12385-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/952d1892710f/ijms-25-12385-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/b9bf5452de94/ijms-25-12385-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/e7e8885d9da9/ijms-25-12385-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/5c618b2a2fce/ijms-25-12385-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/02614d3f3de9/ijms-25-12385-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/952d1892710f/ijms-25-12385-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/b9bf5452de94/ijms-25-12385-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/e7e8885d9da9/ijms-25-12385-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/5c618b2a2fce/ijms-25-12385-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c092/11594342/02614d3f3de9/ijms-25-12385-g005.jpg

相似文献

1
A Snapshot of Early Transcriptional Changes Accompanying the Pro-Neural Phenotype Switch by NGN2, ASCL1, SOX2, and MSI1 in Human Fibroblasts: An RNA-Seq Study.NGN2、ASCL1、SOX2 和 MSI1 诱导人成纤维细胞向神经前体细胞表型转变过程中的早期转录组变化的快照:RNA-Seq 研究。
Int J Mol Sci. 2024 Nov 18;25(22):12385. doi: 10.3390/ijms252212385.
2
Examining the fundamental biology of a novel population of directly reprogrammed human neural precursor cells.探究新型直接重编程人类神经前体细胞群体的基础生物学。
Stem Cell Res Ther. 2019 Jun 13;10(1):166. doi: 10.1186/s13287-019-1255-4.
3
Direct pericyte-to-neuron reprogramming via unfolding of a neural stem cell-like program.通过展开类似神经干细胞的程序实现直接的周细胞到神经元的重编程。
Nat Neurosci. 2018 Jul;21(7):932-940. doi: 10.1038/s41593-018-0168-3. Epub 2018 Jun 18.
4
Neurogenin 2 enhances the generation of patient-specific induced neuronal cells.神经生成素2可增强患者特异性诱导神经元细胞的生成。
Brain Res. 2015 Jul 30;1615:51-60. doi: 10.1016/j.brainres.2015.04.027. Epub 2015 Apr 24.
5
Concise review: the involvement of SOX2 in direct reprogramming of induced neural stem/precursor cells.简明综述:SOX2 在诱导性神经干细胞/前体细胞的直接重编程中的作用。
Stem Cells Transl Med. 2013 Aug;2(8):579-83. doi: 10.5966/sctm.2012-0179. Epub 2013 Jul 1.
6
SOX2 reprograms resident astrocytes into neural progenitors in the adult brain.SOX2 将成年大脑中的星形胶质细胞重编程为神经祖细胞。
Stem Cell Reports. 2015 May 12;4(5):780-94. doi: 10.1016/j.stemcr.2015.03.006. Epub 2015 Apr 23.
7
CEND1 and NEUROGENIN2 Reprogram Mouse Astrocytes and Embryonic Fibroblasts to Induced Neural Precursors and Differentiated Neurons.CEND1 和 NEUROGENIN2 将小鼠星形胶质细胞和胚胎成纤维细胞重编程为诱导性神经前体细胞和分化神经元。
Stem Cell Reports. 2015 Sep 8;5(3):405-18. doi: 10.1016/j.stemcr.2015.07.012. Epub 2015 Aug 28.
8
Making neurons, made easy: The use of Neurogenin-2 in neuronal differentiation.轻松制造神经元:Neurogenin-2 在神经元分化中的应用。
Stem Cell Reports. 2022 Jan 11;17(1):14-34. doi: 10.1016/j.stemcr.2021.11.015. Epub 2021 Dec 30.
9
Dissecting direct reprogramming from fibroblast to neuron using single-cell RNA-seq.利用单细胞RNA测序剖析从成纤维细胞到神经元的直接重编程过程。
Nature. 2016 Jun 16;534(7607):391-5. doi: 10.1038/nature18323. Epub 2016 Jun 8.
10
Generation of induced neuronal cells by the single reprogramming factor ASCL1.由单一重编程因子ASCL1生成诱导神经元细胞。
Stem Cell Reports. 2014 Aug 12;3(2):282-96. doi: 10.1016/j.stemcr.2014.05.020. Epub 2014 Jul 4.