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GATA-3 控制着 TCR 和细胞因子信号下游 T 细胞的维持和增殖。

GATA-3 controls the maintenance and proliferation of T cells downstream of TCR and cytokine signaling.

机构信息

Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

出版信息

Nat Immunol. 2013 Jul;14(7):714-22. doi: 10.1038/ni.2623. Epub 2013 May 26.

Abstract

GATA-3 controls T helper type 2 (TH2) differentiation. However, whether GATA-3 regulates the function of mature T cells beyond TH2 determination remains poorly understood. We found that signaling via the T cell antigen receptor (TCR) and cytokine stimulation promoted GATA-3 expression in CD8(+) T cells, which controlled cell proliferation. Although GATA-3-deficient CD8(+) T cells were generated, their peripheral maintenance was impaired, with lower expression of the receptor for interleukin 7 (IL-7R). GATA-3-deficient T cells had defective responses to viral infection and alloantigen. The proto-oncoprotein c-Myc was a critical target of GATA-3 in promoting T cell proliferation. Our study thus demonstrates an essential role for GATA-3 in controlling the maintenance and proliferation of T cells and provides insight into immunoregulation.

摘要

GATA-3 控制辅助性 T 细胞 2 型(TH2)分化。然而,GATA-3 是否调节成熟 T 细胞的功能,超出 TH2 决定,目前仍了解甚少。我们发现,T 细胞抗原受体(TCR)信号和细胞因子刺激促进 CD8(+)T 细胞中 GATA-3 的表达,控制细胞增殖。尽管生成了 GATA-3 缺陷型 CD8(+)T 细胞,但它们的外周维持受到损害,白细胞介素 7(IL-7R)受体的表达降低。GATA-3 缺陷型 T 细胞对病毒感染和同种异体抗原的反应有缺陷。原癌蛋白 c-Myc 是 GATA-3 促进 T 细胞增殖的关键靶标。因此,我们的研究表明 GATA-3 在控制 T 细胞的维持和增殖方面起着至关重要的作用,并为免疫调节提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87a3/3688666/dc40ea297304/nihms473357f1.jpg

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