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胸腺细胞中对T细胞受体、Notch和阳性选择信号作出反应的不同转录程序。

Distinct transcriptional programs in thymocytes responding to T cell receptor, Notch, and positive selection signals.

作者信息

Huang Yina H, Li Dongling, Winoto Astar, Robey Ellen A

机构信息

Department of Molecular and Cell Biology, Division of Immunology and Cancer Research Laboratory, 475 LSA, University of California, Berkeley, CA 94720, USA.

出版信息

Proc Natl Acad Sci U S A. 2004 Apr 6;101(14):4936-41. doi: 10.1073/pnas.0401133101. Epub 2004 Mar 25.

Abstract

T cell antigen receptor (TCR) signaling is necessary but not sufficient to promote the positive selection of CD4+CD8+ thymocytes into CD4+ or CD8+ mature T cells. Notch signaling has also been implicated as a potential regulator of both CD4/CD8 T cell development and TCR signaling. However, the relationship between positive selection, TCR signaling, and Notch remains unclear. Here we use DNA microarray analysis to compare gene expression changes in CD4+CD8+ double-positive thymocytes undergoing positive selection, TCR stimulation, and Notch activation. We find that the genes induced during positive selection can be resolved into two distinct sets. One set, which we term "TCR-induced," is also induced by in vitro TCR stimulation and contains a large proportion of transcription factors. A second set, which we term "positive-selection-induced," is not induced by in vitro TCR simulation and contains a large proportion of genes involved in signal transduction pathways. Genes induced by Notch activity overlap substantially with genes induced during positive selection. We also find that Notch activity potentiates the effects of TCR stimulation on gene expression. These results help to identify TCR- and positive-selection-specific transcriptional events and help to clarify the relationship between positive selection and Notch.

摘要

T细胞抗原受体(TCR)信号传导对于促进CD4+CD8+胸腺细胞阳性选择成为CD4+或CD8+成熟T细胞是必要的,但并不充分。Notch信号传导也被认为是CD4/CD8 T细胞发育和TCR信号传导的潜在调节因子。然而,阳性选择、TCR信号传导和Notch之间的关系仍不清楚。在此,我们使用DNA微阵列分析来比较经历阳性选择、TCR刺激和Notch激活的CD4+CD8+双阳性胸腺细胞中的基因表达变化。我们发现,在阳性选择过程中诱导的基因可分为两个不同的组。一组我们称为“TCR诱导型”,也可由体外TCR刺激诱导,且包含很大比例的转录因子。另一组我们称为“阳性选择诱导型”,不由体外TCR模拟诱导,且包含很大比例的参与信号转导途径的基因。Notch活性诱导的基因与阳性选择过程中诱导的基因有很大重叠。我们还发现,Notch活性增强了TCR刺激对基因表达的影响。这些结果有助于识别TCR和阳性选择特异性的转录事件,并有助于阐明阳性选择与Notch之间的关系。

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