Generation of four human induced pluripotent stem cell lines from functionally distinct T cell lineages with defined or undefined T cell receptor specificity

IF 0.7 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Marcel Finke , Christopher Kressler , Kristin Fischer , Valeria Fernández Vallone , Ulrik Stervbo , Julian Uszkoreit , Nina Babel , Leila Amini , Michael Schmueck-Henneresse , Harald Stachelscheid , Julia K. Polansky
{"title":"Generation of four human induced pluripotent stem cell lines from functionally distinct T cell lineages with defined or undefined T cell receptor specificity","authors":"Marcel Finke ,&nbsp;Christopher Kressler ,&nbsp;Kristin Fischer ,&nbsp;Valeria Fernández Vallone ,&nbsp;Ulrik Stervbo ,&nbsp;Julian Uszkoreit ,&nbsp;Nina Babel ,&nbsp;Leila Amini ,&nbsp;Michael Schmueck-Henneresse ,&nbsp;Harald Stachelscheid ,&nbsp;Julia K. Polansky","doi":"10.1016/j.scr.2025.103813","DOIUrl":null,"url":null,"abstract":"<div><div>T lymphocytes are key contributors to the adaptive immune system. During development, tightly regulated T cell receptor (TCR) gene rearrangement determines antigen specificity and maturation into distinct lineages with pro- or anti-inflammatory functions. From two male donors, we generated four hiPSC lines from isolated T cell lineages (CD4+ conventional helper, CD4+ regulatory, CD8+ cytotoxic). Two lines harbor genetically pre-rearranged TCRs specific to an allogeneic cell line. All lines were generated by integration-free reprogramming using Sendai virus and underwent characterization and quality control. They represent a valuable platform to investigate how a rearranged and pre-selected TCR influences lymphoid differentiation and function.</div></div>","PeriodicalId":21843,"journal":{"name":"Stem cell research","volume":"88 ","pages":"Article 103813"},"PeriodicalIF":0.7000,"publicationDate":"2025-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stem cell research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1873506125001631","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

T lymphocytes are key contributors to the adaptive immune system. During development, tightly regulated T cell receptor (TCR) gene rearrangement determines antigen specificity and maturation into distinct lineages with pro- or anti-inflammatory functions. From two male donors, we generated four hiPSC lines from isolated T cell lineages (CD4+ conventional helper, CD4+ regulatory, CD8+ cytotoxic). Two lines harbor genetically pre-rearranged TCRs specific to an allogeneic cell line. All lines were generated by integration-free reprogramming using Sendai virus and underwent characterization and quality control. They represent a valuable platform to investigate how a rearranged and pre-selected TCR influences lymphoid differentiation and function.
从功能不同的T细胞系中产生四种人类诱导多能干细胞系,具有定义或未定义的T细胞受体特异性
T淋巴细胞是适应性免疫系统的关键贡献者。在发育过程中,严格调控的T细胞受体(TCR)基因重排决定了抗原特异性和成熟成具有促炎或抗炎功能的不同谱系。从两名男性供体中,我们从分离的T细胞系(CD4+常规辅助细胞,CD4+调节细胞,CD8+细胞毒性细胞)中产生了四个hiPSC系。两种细胞系含有同种异体细胞系特有的基因预先重排的tcr。所有系均通过仙台病毒无整合重编程生成,并进行了鉴定和质量控制。它们为研究重排和预先选择的TCR如何影响淋巴细胞分化和功能提供了一个有价值的平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Stem cell research
Stem cell research 生物-生物工程与应用微生物
CiteScore
2.20
自引率
8.30%
发文量
338
审稿时长
55 days
期刊介绍: Stem Cell Research is dedicated to publishing high-quality manuscripts focusing on the biology and applications of stem cell research. Submissions to Stem Cell Research, may cover all aspects of stem cells, including embryonic stem cells, tissue-specific stem cells, cancer stem cells, developmental studies, stem cell genomes, and translational research. Stem Cell Research publishes 6 issues a year.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信