• 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

早期 T 细胞发育途径:表观遗传和转录因子之间的串扰。

The Route of Early T Cell Development: Crosstalk between Epigenetic and Transcription Factors.

机构信息

Department of Human Genetics, Leiden University Medical Centre (LUMC), 2300 RC Leiden, The Netherlands.

Department of Immunology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

出版信息

Cells. 2021 Apr 30;10(5):1074. doi: 10.3390/cells10051074.

DOI:10.3390/cells10051074
PMID:33946533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8147249/
Abstract

Hematopoietic multipotent progenitors seed the thymus and then follow consecutive developmental stages until the formation of mature T cells. During this process, phenotypic changes of T cells entail stage-specific transcriptional programs that underlie the dynamic progression towards mature lymphocytes. Lineage-specific transcription factors are key drivers of T cell specification and act in conjunction with epigenetic regulators that have also been elucidated as crucial players in the establishment of regulatory networks necessary for proper T cell development. In this review, we summarize the activity of transcription factors and epigenetic regulators that together orchestrate the intricacies of early T cell development with a focus on regulation of T cell lineage commitment.

摘要

造血多能祖细胞定植于胸腺,然后经历连续的发育阶段,直至成熟 T 细胞的形成。在此过程中,T 细胞的表型变化需要特定于阶段的转录程序,这些程序是向成熟淋巴细胞动态进展的基础。谱系特异性转录因子是 T 细胞特化的关键驱动因素,它们与表观遗传调节剂协同作用,这些调节剂也被阐明为建立适当 T 细胞发育所需的调控网络的关键因素。在这篇综述中,我们总结了转录因子和表观遗传调节剂的活性,它们共同协调早期 T 细胞发育的复杂性,重点是 T 细胞谱系决定的调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a727/8147249/8d9882a0be24/cells-10-01074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a727/8147249/ad86144516ca/cells-10-01074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a727/8147249/8d9882a0be24/cells-10-01074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a727/8147249/ad86144516ca/cells-10-01074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a727/8147249/8d9882a0be24/cells-10-01074-g002.jpg

相似文献

1
The Route of Early T Cell Development: Crosstalk between Epigenetic and Transcription Factors.早期 T 细胞发育途径:表观遗传和转录因子之间的串扰。
Cells. 2021 Apr 30;10(5):1074. doi: 10.3390/cells10051074.
2
Genetic and epigenetic control of early lymphocyte development.早期淋巴细胞发育的遗传和表观遗传控制。
Curr Top Microbiol Immunol. 2014;381:1-20. doi: 10.1007/82_2014_370.
3
Epigenetic Dynamics in the Function of T-Lineage Regulatory Factor Bcl11b.Bcl11b 转录因子功能中的表观遗传动态
Front Immunol. 2021 Apr 14;12:669498. doi: 10.3389/fimmu.2021.669498. eCollection 2021.
4
Mi-2/NuRD chromatin remodeling complexes regulate B and T-lymphocyte development and function.Mi-2/NuRD染色质重塑复合物调控B淋巴细胞和T淋巴细胞的发育与功能。
Immunol Rev. 2014 Sep;261(1):126-40. doi: 10.1111/imr.12209.
5
Epigenetic events during B lymphocyte development.B 淋巴细胞发育过程中的表观遗传事件。
Epigenetics. 2009 Oct 1;4(7):462-8. doi: 10.4161/epi.4.7.10052.
6
From hematopoietic progenitors to B cells: mechanisms of lineage restriction and commitment.从造血祖细胞到 B 细胞:谱系限制和定向的机制。
Curr Opin Immunol. 2010 Apr;22(2):177-84. doi: 10.1016/j.coi.2010.02.003. Epub 2010 Mar 6.
7
Dynamic Transcriptome, DNA Methylome, and DNA Hydroxymethylome Networks During T-Cell Lineage Commitment.T 细胞谱系定向过程中的动态转录组、DNA 甲基化组和 DNA 羟甲基化组网络。
Mol Cells. 2018 Nov 30;41(11):953-963. doi: 10.14348/molcells.2018.0213. Epub 2018 Nov 1.
8
An early T cell lineage commitment checkpoint dependent on the transcription factor Bcl11b.早期 T 细胞谱系决定检查点依赖于转录因子 Bcl11b。
Science. 2010 Jul 2;329(5987):89-93. doi: 10.1126/science.1188989.
9
At the crossroads: diverse roles of early thymocyte transcriptional regulators.十字路口:早期胸腺细胞转录调节因子的多样作用
Immunol Rev. 2006 Feb;209:191-211. doi: 10.1111/j.0105-2896.2006.00352.x.
10
Deciphering the Complexity of 3D Chromatin Organization Driving Lymphopoiesis and Lymphoid Malignancies.解析驱动淋巴发生和淋巴恶性肿瘤的三维染色质组织复杂性。
Front Immunol. 2021 May 14;12:669881. doi: 10.3389/fimmu.2021.669881. eCollection 2021.

引用本文的文献

1
The Proteomics of T-Cell and Early T-Cell Precursor (ETP) Acute Lymphocytic Leukemia: Prognostic Patterns in Adult and Pediatric-ETP ALL.T细胞和早期T细胞前体(ETP)急性淋巴细胞白血病的蛋白质组学:成人和儿童ETP急性淋巴细胞白血病的预后模式
Cancers (Basel). 2024 Dec 19;16(24):4241. doi: 10.3390/cancers16244241.
2
SATB1 prevents immune cell infiltration by regulating chromatin organization and gene expression of a chemokine gene cluster in T cells.SATB1 通过调节 T 细胞中趋化因子基因簇的染色质组织和基因表达来防止免疫细胞浸润。
Commun Biol. 2024 Oct 11;7(1):1304. doi: 10.1038/s42003-024-07021-8.
3
Decreased TCF1 and BCL11B expression predicts poor prognosis for patients with chronic lymphocytic leukemia.

本文引用的文献

1
Epigenetic Regulators as the Gatekeepers of Hematopoiesis.表观遗传调控因子作为造血作用的守门人
Trends Genet. 2020 Oct 21. doi: 10.1016/j.tig.2020.09.015.
2
Transcription factors regulate early T cell development via redeployment of other factors: Functional dynamics of constitutively required factors in cell fate decisions.转录因子通过重新分配其他因子来调节早期 T 细胞发育:细胞命运决定中固有必需因子的功能动态。
Bioessays. 2021 May;43(5):e2000345. doi: 10.1002/bies.202000345. Epub 2021 Feb 24.
3
Runx1 and Runx3 drive progenitor to T-lineage transcriptome conversion in mouse T cell commitment via dynamic genomic site switching.
TCF1 和 BCL11B 表达降低预示慢性淋巴细胞白血病患者预后不良。
Front Immunol. 2022 Sep 23;13:985280. doi: 10.3389/fimmu.2022.985280. eCollection 2022.
4
Integration of Transcriptome and Interactome Predicts an ETP-ALL-Specific Transcriptional Footprint that Decodes its Developmental Propensity.转录组与相互作用组的整合预测了一种ETP-ALL特异性转录足迹,该足迹可解码其发育倾向。
Front Cell Dev Biol. 2022 May 13;10:899752. doi: 10.3389/fcell.2022.899752. eCollection 2022.
5
Human Transcriptome Array Analysis Identifies CDR2 as a Novel Suppressed Gene for Kawasaki Disease.人类转录组阵列分析确定CDR2为川崎病的一个新的受抑制基因。
Diagnostics (Basel). 2022 Jan 19;12(2):240. doi: 10.3390/diagnostics12020240.
Runx1 和 Runx3 通过动态基因组位点转换驱动祖细胞向 T 细胞谱系转录组转换,从而促进小鼠 T 细胞的定型。
Proc Natl Acad Sci U S A. 2021 Jan 26;118(4). doi: 10.1073/pnas.2019655118.
4
Multi-scale Dynamical Modeling of T Cell Development from an Early Thymic Progenitor State to Lineage Commitment.多尺度动力学模型研究从早期胸腺祖细胞状态到谱系定型的 T 细胞发育
Cell Rep. 2021 Jan 12;34(2):108622. doi: 10.1016/j.celrep.2020.108622.
5
Loss of MBD2 affects early T cell development by inhibiting the WNT signaling pathway.MBD2 的缺失通过抑制 WNT 信号通路影响早期 T 细胞的发育。
Exp Cell Res. 2021 Jan 1;398(1):112400. doi: 10.1016/j.yexcr.2020.112400. Epub 2020 Nov 30.
6
How transcription factors drive choice of the T cell fate.转录因子如何驱动 T 细胞命运的选择。
Nat Rev Immunol. 2021 Mar;21(3):162-176. doi: 10.1038/s41577-020-00426-6. Epub 2020 Sep 11.
7
Pioneer Transcription Factors Initiating Gene Network Changes.先驱转录因子引发基因网络变化。
Annu Rev Genet. 2020 Nov 23;54:367-385. doi: 10.1146/annurev-genet-030220-015007. Epub 2020 Sep 4.
8
Functional definition of a transcription factor hierarchy regulating T cell lineage commitment.调控T细胞谱系定向的转录因子层级结构的功能定义。
Sci Adv. 2020 Jul 31;6(31):eaaw7313. doi: 10.1126/sciadv.aaw7313. eCollection 2020 Jul.
9
UHRF1 Controls Thymocyte Fate Decisions through the Epigenetic Regulation of EGR1 Expression.UHRF1 通过表观遗传调控 EGR1 表达控制胸腺细胞命运决定。
J Immunol. 2020 Jun 15;204(12):3248-3261. doi: 10.4049/jimmunol.1901471. Epub 2020 May 1.
10
Epigenetics of T cell fate decision.T细胞命运决定的表观遗传学
Curr Opin Immunol. 2020 Apr;63:43-50. doi: 10.1016/j.coi.2020.01.002. Epub 2020 Feb 15.