A190:进化小鼠调节性t细胞中foxp3依赖性和非依赖性基因表达的调控机制

A. Glasner, Y. Zhong, J. V. D. Veeken, A. Rudensky
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引用次数: 0

摘要

表达叉头盒转录因子(Foxp3)的T调节细胞(Treg)是重要的免疫调节细胞,通过控制效应T细胞的活性在肿瘤和转移中起关键作用。谱系指定转录因子(TFs)建立细胞身份并维持细胞特异性转录程序。Foxp3是控制Treg细胞各种发育和功能模式的关键主控TF。人类和小鼠的Foxp3缺乏会导致危及生命的自身免疫性疾病,而Foxp3在CD4+ t细胞中的强制表达赋予了抑制功能。然而,我们对胸腺分化过程中Treg细胞的调控,以及周围成熟的Treg细胞,无论是依赖还是独立的Foxp3,仍然缺乏了解。单核苷酸多态性(snp)可能发生在编码基因或非编码基因组调控区域,并可能导致严重的表型后果。我们最近试图将snp与人类Treg转录组和表观遗传特征的差异联系起来。然而,这类研究受到其内在相关性和snp数量有限的限制。在这里,我们使用进化距离较远的小鼠菌株C57Bl/6 (B6)、CAST/EiJ (CAST)和SPRET/EiJ (SPRET),来鉴定Treg细胞及其前体在分化和各种条件下转录和表观遗传程序中的等位基因特异性失衡和功能差异。利用Foxp3报告基因和条件敲除(conditional knockout, KO)系统,结合进化远缘小鼠的体内杂交,采用RNA-seq、ATAC-seq和Chip-seq等高通量基因组方法,探讨Treg细胞分化和功能的遗传和分子机制。这些研究可能为开发新的治疗方法来治疗癌症和转移铺平道路。引文格式:Ariella Glasner, Yi Zhong, Joris Van Der Veeken, Alexander Rudensky。进化远缘小鼠调节性t细胞中foxp3依赖性和非依赖性基因表达的调控机制[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志,2019;7(2增刊):摘要nr A190。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract A190: Mechanisms governing Foxp3-dependent and -independent gene expression in regulatory T-cells in evolutionary distant mice
T regulatory (Treg) cells expressing the forkhead box transcription factor (Foxp3) are important regulators of immunity and play a key role in cancer and metastasis by controlling the activity of effector T-cells. Lineage-specifying transcription factors (TFs) establish cell identity and maintain cell specific transcriptional programs. Foxp3 is a key master TF controlling various Treg cell developmental and functional modalities. Foxp3 deficiency in humans and mice causes a life threatening autoimmune disease, and the enforced expression of Foxp3 in CD4+ T-cells confers suppressor functions. However, our understanding of Treg cell regulation during differentiation in the thymus, and in mature Treg cells in the periphery, whether Foxp3 dependent or independent, is still lacking. Single-nucleotide polymorphism (SNPs) may occur within coding genes or noncoding genomic regulatory areas and can have severe phenotypic consequences. We have recently attempted to link SNPs with differential Treg transcriptomic and epigenetic features in humans. However, such studies are limited by their intrinsic correlative nature, and by the limited number of SNPs. Here we use evolutionally distant mice strains C57Bl/6 (B6), CAST/EiJ (Cast) and SPRET/EiJ (Spret), to identify allele-specific imbalances and functional differences in the transcriptional and epigenetic programs during differentiation and in various conditions of Treg cells and their precursors. Using Foxp3 reporter and conditional knockout (KO) systems combined with interbreeding of the evolutionary distant mice strains in vivo, we explore the genetic and molecular mechanisms of Treg cell differentiation and function, employing high-throughput genomic methods including RNA-seq, ATAC-seq and Chip-seq. Such studies may pave a way for the development of novel therapeutic approaches to treat cancer and metastasis. Citation Format: Ariella Glasner, Yi Zhong, Joris Van Der Veeken, Alexander Rudensky. Mechanisms governing Foxp3-dependent and -independent gene expression in regulatory T-cells in evolutionary distant mice [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A190.
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