• 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

人 T 细胞发育过程中的 Notch 信号通路。

Notch signaling during human T cell development.

机构信息

Department of Clinical Chemistry, Microbiology and Immunology, Ghent University Hospital, Ghent University, 9000 Ghent, Belgium.

出版信息

Curr Top Microbiol Immunol. 2012;360:75-97. doi: 10.1007/82_2012_230.

DOI:10.1007/82_2012_230
PMID:22692833
Abstract

Notch signaling is critical during multiple stages of T cell development in both mouse and human. Evidence has emerged in recent years that this pathway might regulate T-lineage differentiation differently between both species. Here, we review our current understanding of how Notch signaling is activated and used during human T cell development. First, we set the stage by describing the developmental steps that make up human T cell development before describing the expression profiles of Notch receptors, ligands, and target genes during this process. To delineate stage-specific roles for Notch signaling during human T cell development, we subsequently try to interpret the functional Notch studies that have been performed in light of these expression profiles and compare this to its suggested role in the mouse.

摘要

Notch 信号通路在人和小鼠的 T 细胞发育的多个阶段都至关重要。近年来的证据表明,该通路可能在两种物种之间调节 T 细胞谱系分化的方式存在差异。在这里,我们综述了目前对于 Notch 信号通路在人类 T 细胞发育过程中如何被激活和使用的理解。首先,我们在描述 Notch 受体、配体和靶基因在这一过程中的表达谱之前,先描述了组成人类 T 细胞发育的发育步骤。为了阐明 Notch 信号在人类 T 细胞发育过程中的特定阶段的作用,我们随后尝试根据这些表达谱来解释已完成的 Notch 功能研究,并将其与在小鼠中的作用进行比较。

相似文献

1
Notch signaling during human T cell development.人 T 细胞发育过程中的 Notch 信号通路。
Curr Top Microbiol Immunol. 2012;360:75-97. doi: 10.1007/82_2012_230.
2
Stage-specific and differential notch dependency at the alphabeta and gammadelta T lineage bifurcation.αβ和γδ T细胞谱系分化过程中的阶段特异性和差异性Notch依赖性
Immunity. 2006 Jul;25(1):105-16. doi: 10.1016/j.immuni.2006.05.010. Epub 2006 Jun 29.
3
Notch receptor-ligand interactions during T cell development, a ligand endocytosis-driven mechanism.Notch 受体-配体相互作用在 T 细胞发育过程中,是一种配体内吞驱动的机制。
Curr Top Microbiol Immunol. 2012;360:19-46. doi: 10.1007/82_2012_225.
4
Notch regulation of early thymocyte development.Notch 调控早期胸腺细胞发育。
Semin Immunol. 2010 Oct;22(5):261-9. doi: 10.1016/j.smim.2010.04.015. Epub 2010 Jul 13.
5
Biomaterial-based notch signaling for the differentiation of hematopoietic stem cells into T cells.基于生物材料的Notch信号传导促进造血干细胞分化为T细胞。
J Biomed Mater Res A. 2006 Dec 1;79(3):689-97. doi: 10.1002/jbm.a.30916.
6
Delta-like 4-mediated Notch signaling is required for early T-cell development in a three-dimensional thymic structure.Delta样4介导的Notch信号对于三维胸腺结构中早期T细胞发育是必需的。
Eur J Immunol. 2015 Aug;45(8):2252-62. doi: 10.1002/eji.201445123. Epub 2015 Jun 3.
7
Ongoing Dll4-Notch signaling is required for T-cell homeostasis in the adult thymus.持续的 Dll4-Notch 信号传导是成年胸腺中 T 细胞稳态所必需的。
Eur J Immunol. 2011 Aug;41(8):2207-16. doi: 10.1002/eji.201041343. Epub 2011 Jul 4.
8
TCR and Notch signaling in CD4 and CD8 T-cell development.CD4和CD8 T细胞发育过程中的TCR和Notch信号传导。
Immunol Rev. 2006 Feb;209:274-83. doi: 10.1111/j.0105-2896.2006.00358.x.
9
Differential requirements for Wnt and Notch signaling in hematopoietic versus thymic niches.造血微环境与胸腺微环境中 Wnt 和 Notch 信号的差异需求。
Ann N Y Acad Sci. 2012 Aug;1266:78-93. doi: 10.1111/j.1749-6632.2012.06626.x.
10
Immunology. Keeping a tight leash on Notch.免疫学。严格控制Notch信号通路。
Science. 2007 May 11;316(5826):840-2. doi: 10.1126/science.1143336.

引用本文的文献

1
T Cell Development: From T-Lineage Specification to Intrathymic Maturation.T细胞发育:从T细胞谱系特化到胸腺内成熟
Adv Exp Med Biol. 2025;1471:81-137. doi: 10.1007/978-3-031-77921-3_4.
2
Unlocking the potential of iPSC-derived immune cells: engineering iNK and iT cells for cutting-edge immunotherapy.释放诱导多能干细胞衍生免疫细胞的潜力:工程化诱导自然杀伤细胞和诱导性T细胞用于前沿免疫疗法。
Front Immunol. 2024 Aug 30;15:1457629. doi: 10.3389/fimmu.2024.1457629. eCollection 2024.
3
Intrathymic dendritic cell-biased precursors promote human T cell lineage specification through IRF8-driven transmembrane TNF.
胸腺内树突状细胞偏向前体细胞通过 IRF8 驱动的跨膜 TNF 促进人类 T 细胞谱系特化。
Nat Immunol. 2023 Mar;24(3):474-486. doi: 10.1038/s41590-022-01417-6. Epub 2023 Jan 26.
4
In Vitro Model Systems to Study Human T Cell Development.体外模型系统研究人类 T 细胞发育。
Methods Mol Biol. 2023;2580:335-354. doi: 10.1007/978-1-0716-2740-2_21.
5
Identification and Purification of Human T Cell Precursors.人 T 细胞前体的鉴定与纯化。
Methods Mol Biol. 2023;2580:315-333. doi: 10.1007/978-1-0716-2740-2_20.
6
The immune landscape of human thymic epithelial tumors.人类胸腺上皮肿瘤的免疫景观。
Nat Commun. 2022 Sep 17;13(1):5463. doi: 10.1038/s41467-022-33170-7.
7
Small RNA-Seq Reveals Similar miRNA Transcriptome in Children and Young Adults with T-ALL and Indicates miR-143-3p as Novel Candidate Tumor Suppressor in This Leukemia.Small RNA-Seq 揭示儿童和青年 T-ALL 患者 miRNA 转录组相似,并表明 miR-143-3p 是这种白血病的新型候选肿瘤抑制因子。
Int J Mol Sci. 2022 Sep 4;23(17):10117. doi: 10.3390/ijms231710117.
8
Transcriptional dynamics and epigenetic regulation of E and ID protein encoding genes during human T cell development.人类 T 细胞发育过程中 E 和 ID 蛋白编码基因的转录动态和表观遗传调控。
Front Immunol. 2022 Jul 28;13:960918. doi: 10.3389/fimmu.2022.960918. eCollection 2022.
9
Patterns of Differentially Expressed circRNAs in Human Thymocytes.人类胸腺细胞中差异表达的环状RNA模式
Noncoding RNA. 2022 Mar 30;8(2):26. doi: 10.3390/ncrna8020026.
10
A DL-4- and TNFα-based culture system to generate high numbers of nonmodified or genetically modified immunotherapeutic human T-lymphoid progenitors.一种基于 DL-4 和 TNFα 的培养系统,可生成大量未经修饰或基因修饰的免疫治疗性人 T 淋巴细胞祖细胞。
Cell Mol Immunol. 2021 Jul;18(7):1662-1676. doi: 10.1038/s41423-021-00706-8. Epub 2021 Jun 11.