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IL-2 依赖性 NK 细胞动态平衡的适应性控制。

IL-2-dependent adaptive control of NK cell homeostasis.

机构信息

Howard Hughes Medical Institute, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

出版信息

J Exp Med. 2013 Jun 3;210(6):1179-87. doi: 10.1084/jem.20122571. Epub 2013 May 6.

Abstract

Activation and expansion of T and B lymphocytes and myeloid cells are controlled by Foxp3(+) regulatory T cells (T reg cells), and their deficiency results in a fatal lympho- and myeloproliferative syndrome. A role for T reg cells in the homeostasis of innate lymphocyte lineages remained unknown. Here, we report that T reg cells restrained the expansion of immature CD127(+) NK cells, which had the unique ability to up-regulate the IL2Rα (CD25) in response to the proinflammatory cytokine IL-12. In addition, we observed the preferential accumulation of CD127(+) NK cells in mice bearing progressing tumors or suffering from chronic viral infection. CD127(+) NK cells expanded in an IL-2-dependent manner upon T reg cell depletion and were able to give rise to mature NK cells, indicating that the latter can develop through a CD25(+) intermediate stage. Thus, T reg cells restrain the IL-2-dependent CD4(+) T cell help for CD127(+) immature NK cells. These findings highlight the adaptive control of innate lymphocyte homeostasis.

摘要

T 和 B 淋巴细胞以及髓系细胞的激活和扩增受 Foxp3(+)调节性 T 细胞(Treg 细胞)控制,其缺失会导致致命的淋巴和骨髓增生性综合征。Treg 细胞在固有淋巴细胞谱系的稳态中的作用尚不清楚。在这里,我们报告 Treg 细胞抑制了不成熟 CD127(+)NK 细胞的扩增,后者具有独特的能力,能够在促炎细胞因子 IL-12 的作用下上调 IL2Rα(CD25)。此外,我们观察到携带进展性肿瘤或患有慢性病毒感染的小鼠中 CD127(+)NK 细胞的优先积累。在 Treg 细胞耗竭后,CD127(+)NK 细胞以依赖 IL-2 的方式扩增,并能够产生成熟的 NK 细胞,这表明后者可以通过 CD25(+)中间阶段发育。因此,Treg 细胞抑制了 CD127(+)未成熟 NK 细胞的 IL-2 依赖性 CD4(+)T 细胞辅助作用。这些发现强调了固有淋巴细胞稳态的适应性控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8582/3674698/65155bdeaa91/JEM_20122571_Fig1.jpg

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