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Cutting edge: A double-mutant knockin of the CD28 YMNM and PYAP motifs reveals a critical role for the YMNM motif in regulation of T cell proliferation and Bcl-xL expression.前沿:CD28 YMNM 和 PYAP 基序的双突变敲入揭示了 YMNM 基序在调节 T 细胞增殖和 Bcl-xL 表达中的关键作用。
J Immunol. 2014 Apr 15;192(8):3465-9. doi: 10.4049/jimmunol.1301240. Epub 2014 Mar 17.
2
Targeted knock-in mice expressing mutations of CD28 reveal an essential pathway for costimulation.表达CD28突变的靶向敲入小鼠揭示了共刺激的一条重要途径。
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本文引用的文献

1
CTLA4Ig inhibits effector T cells through regulatory T cells and TGF-β.CTLA4Ig 通过调节性 T 细胞和 TGF-β 抑制效应 T 细胞。
J Immunol. 2013 Sep 15;191(6):3082-9. doi: 10.4049/jimmunol.1300830. Epub 2013 Aug 16.
2
CD28 promotes CD4+ T cell clonal expansion during infection independently of its YMNM and PYAP motifs.CD28 在感染过程中通过其 YMNM 和 PYAP 基序独立促进 CD4+ T 细胞克隆扩增。
J Immunol. 2012 Sep 15;189(6):2909-17. doi: 10.4049/jimmunol.1103231. Epub 2012 Aug 15.
3
An enigmatic tail of CD28 signaling.CD28 信号的神秘尾巴。
Cold Spring Harb Perspect Biol. 2010 Aug;2(8):a002436. doi: 10.1101/cshperspect.a002436. Epub 2010 Jun 9.
4
CTLA4-Ig inhibits allergic airway inflammation by a novel CD28-independent, nitric oxide synthase-dependent mechanism.CTLA4-Ig通过一种新的不依赖CD28、依赖一氧化氮合酶的机制抑制过敏性气道炎症。
Eur J Immunol. 2010 Jul;40(7):1985-94. doi: 10.1002/eji.200940282.
5
CD28 facilitates the generation of Foxp3(-) cytokine responsive regulatory T cell precursors.CD28 有助于 Foxp3(-)细胞因子反应性调节性 T 细胞前体的生成。
J Immunol. 2010 Jun 1;184(11):6007-13. doi: 10.4049/jimmunol.1000019. Epub 2010 Apr 26.
6
The clinical utility of inhibiting CD28-mediated costimulation.抑制CD28介导的共刺激的临床应用。
Immunol Rev. 2009 May;229(1):307-21. doi: 10.1111/j.1600-065X.2009.00780.x.
7
Targeted knock-in mice expressing mutations of CD28 reveal an essential pathway for costimulation.表达CD28突变的靶向敲入小鼠揭示了共刺激的一条重要途径。
Mol Cell Biol. 2009 Jul;29(13):3710-21. doi: 10.1128/MCB.01869-08. Epub 2009 Apr 27.
8
CD28 interaction with filamin-A controls lipid raft accumulation at the T-cell immunological synapse.CD28与细丝蛋白A的相互作用控制脂质筏在T细胞免疫突触处的积累。
Nat Cell Biol. 2006 Nov;8(11):1270-6. doi: 10.1038/ncb1492. Epub 2006 Oct 22.
9
A dose-dependent requirement for the proline motif of CD28 in cellular and humoral immunity revealed by a targeted knockin mutant.靶向敲入突变体揭示CD28脯氨酸基序在细胞免疫和体液免疫中的剂量依赖性需求。
J Exp Med. 2006 Sep 4;203(9):2121-33. doi: 10.1084/jem.20052230. Epub 2006 Aug 14.
10
Abatacept for rheumatoid arthritis refractory to tumor necrosis factor alpha inhibition.阿巴西普用于对肿瘤坏死因子α抑制治疗无效的类风湿关节炎。
N Engl J Med. 2005 Sep 15;353(11):1114-23. doi: 10.1056/NEJMoa050524.

前沿:CD28 YMNM 和 PYAP 基序的双突变敲入揭示了 YMNM 基序在调节 T 细胞增殖和 Bcl-xL 表达中的关键作用。

Cutting edge: A double-mutant knockin of the CD28 YMNM and PYAP motifs reveals a critical role for the YMNM motif in regulation of T cell proliferation and Bcl-xL expression.

机构信息

Department of Internal Medicine, Washington University School of Medicine, St Louis, MO 63110.

出版信息

J Immunol. 2014 Apr 15;192(8):3465-9. doi: 10.4049/jimmunol.1301240. Epub 2014 Mar 17.

DOI:10.4049/jimmunol.1301240
PMID:24639356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3994466/
Abstract

CD28 is a critical regulator of T cell function, augmenting proliferation, cytokine secretion, and cell survival. Our previous work using knockin mice expressing point mutations in CD28 demonstrated that the distal proline motif was primarily responsible for much of CD28 function, whereas in marked contrast to prior studies, mutation of the PI3K-binding motif had little discernible effect. In this study, we examined the phenotype of mice in which both motifs are simultaneously mutated. We found that mutation of the PYAP motif unmasks a critical role for the proximal tyrosine motif in regulating T cell proliferation and expression of Bcl-xL but not cytokine secretion. In addition, we demonstrated that, although function is more severely impaired in the double mutant than in either single mutant, there remained residual CD28-dependent responses, definitively establishing that additional motifs can partially mediate CD28 function.

摘要

CD28 是 T 细胞功能的关键调节因子,可增强增殖、细胞因子分泌和细胞存活。我们之前使用表达 CD28 点突变的基因敲入小鼠的研究表明,远端脯氨酸基序主要负责 CD28 的大部分功能,而与先前的研究形成鲜明对比的是,PI3K 结合基序的突变几乎没有明显影响。在这项研究中,我们检查了两个基序同时突变的小鼠表型。我们发现,PYAP 基序的突变揭示了近端酪氨酸基序在调节 T 细胞增殖和 Bcl-xL 表达中的关键作用,但对细胞因子分泌没有影响。此外,我们证明,尽管双突变体的功能比单个突变体严重受损,但仍存在残留的 CD28 依赖性反应,明确证实了其他基序可以部分介导 CD28 功能。