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J Exp Med. 2011 Oct 24;208(11):2183-91. doi: 10.1084/jem.20102191. Epub 2011 Sep 26.
2
T-cell tolerance and the multi-functional role of IL-2R signaling in T-regulatory cells.T 细胞耐受与 IL-2R 信号在 T 调节细胞中的多功能作用。
Immunol Rev. 2011 May;241(1):63-76. doi: 10.1111/j.1600-065X.2011.01004.x.
3
Signaling in thymic selection.胸腺选择中的信号转导。
Curr Opin Immunol. 2011 Apr;23(2):207-12. doi: 10.1016/j.coi.2010.12.017. Epub 2011 Jan 15.
4
Becoming self-aware: the thymic education of regulatory T cells.成为有自我意识的:调节性 T 细胞的胸腺教育。
Curr Opin Immunol. 2011 Apr;23(2):213-9. doi: 10.1016/j.coi.2010.11.010. Epub 2010 Dec 14.
5
A tale of two TRAPs: LAT and LAB in the regulation of lymphocyte development, activation, and autoimmunity.两段 TRAP:LAT 和 LAB 在淋巴细胞发育、激活和自身免疫中的调节作用。
Immunol Res. 2011 Apr;49(1-3):97-108. doi: 10.1007/s12026-010-8197-3.
6
Graded attenuation of TCR signaling elicits distinct autoimmune diseases by altering thymic T cell selection and regulatory T cell function.TCR 信号的分级衰减通过改变胸腺 T 细胞选择和调节性 T 细胞功能引发不同的自身免疫性疾病。
J Immunol. 2010 Aug 15;185(4):2295-305. doi: 10.4049/jimmunol.1000848. Epub 2010 Jul 19.
7
The role of the LAT-PLC-gamma1 interaction in T regulatory cell function.LAT-PLC-gamma1 相互作用在调节性 T 细胞功能中的作用。
J Immunol. 2010 Mar 1;184(5):2476-86. doi: 10.4049/jimmunol.0902876. Epub 2010 Feb 3.
8
Phospholipase C{gamma}1 is essential for T cell development, activation, and tolerance.PLCγ1 对于 T 细胞的发育、激活和耐受是必需的。
J Exp Med. 2010 Feb 15;207(2):309-18. doi: 10.1084/jem.20090880. Epub 2010 Feb 1.
9
Unaltered negative selection and Treg development of self-reactive thymocytes in TCR transgenic Fyn-deficient mice.TCR 转基因 Fyn 缺陷型小鼠中自身反应性胸腺细胞的未改变的阴性选择和 Treg 发育。
Eur J Immunol. 2010 Feb;40(2):539-47. doi: 10.1002/eji.200939645.
10
A hypomorphic allele of ZAP-70 reveals a distinct thymic threshold for autoimmune disease versus autoimmune reactivity.ZAP-70的一个低表达等位基因揭示了自身免疫性疾病与自身免疫反应性的不同胸腺阈值。
J Exp Med. 2009 Oct 26;206(11):2527-41. doi: 10.1084/jem.20082902. Epub 2009 Oct 19.

T 细胞受体信号转导调控胸腺内天然调节性 T 细胞的发育。

T cell receptor signaling that regulates the development of intrathymic natural regulatory T cells.

机构信息

Center for Agricultural Biomaterials, Seoul National University, Seoul 151-921, Korea.

出版信息

Immune Netw. 2011 Dec;11(6):336-41. doi: 10.4110/in.2011.11.6.336. Epub 2011 Dec 31.

DOI:10.4110/in.2011.11.6.336
PMID:22346772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3275701/
Abstract

T cell receptor (TCR) signaling plays a critical role in T cell development, survival and differentiation. In the thymus, quantitative and/or qualitative differences in TCR signaling determine the fate of developing thymocytes and lead to positive and negative selection. Recently, it has been suggested that self-reactive T cells, escape from negative selection, should be suppressed in the periphery by regulatory T cells (Tregs) expressing Foxp3 transcription factor. Foxp3 is a master factor that is critical for not only development and survival but also suppressive activity of Treg. However, signals that determine Treg fate are not completely understood. The availability of mutant mice which harbor mutations in TCR signaling mediators will certainly allow to delineate signaling events that control intrathymic (natural) Treg (nTreg) development. Thus, we summarize the recent progress on the role of TCR signaling cascade components in nTreg development from the studies with murine model.

摘要

T 细胞受体(TCR)信号在 T 细胞的发育、存活和分化中起着关键作用。在胸腺中,TCR 信号的数量和/或质量差异决定了发育中的胸腺细胞的命运,并导致阳性和阴性选择。最近,有人提出,逃避负选择的自身反应性 T 细胞应该被表达 Foxp3 转录因子的调节性 T 细胞(Treg)在周围组织中抑制。Foxp3 是一个关键的主调控因子,不仅对 Treg 的发育和存活至关重要,而且对其抑制活性也至关重要。然而,决定 Treg 命运的信号还不完全清楚。TCR 信号转导介质突变小鼠的出现,必将有助于描绘控制胸腺内(天然)调节性 T 细胞(nTreg)发育的信号事件。因此,我们从鼠模型的研究中总结了 TCR 信号级联成分在 nTreg 发育中的作用的最新进展。