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自然杀伤T细胞的转录程序。

The transcriptional programs of iNKT cells.

作者信息

Kim Edy Y, Lynch Lydia, Brennan Patrick J, Cohen Nadia R, Brenner Michael B

机构信息

Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, 15 Francis Street, Boston, MA 02115, United States; Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Smith Building, 5th Floor, 1 Jimmy Fund Way, Boston, MA 02115, United States.

Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Smith Building, 5th Floor, 1 Jimmy Fund Way, Boston, MA 02115, United States; Division of Endocrinology, Diabetes and Hypertension, Brigham and Women's Hospital, 221 Longwood Avenue, Boston, MA 02115, United States.

出版信息

Semin Immunol. 2015 Feb;27(1):26-32. doi: 10.1016/j.smim.2015.02.005. Epub 2015 Apr 2.

Abstract

Invariant natural killer T (iNKT) cells are innate T cells that express a semi-invariant T cell receptor (TCR) and recognize lipid antigens presented by CD1d molecules. As part of innate immunity, iNKT cells rapidly produce large amounts of cytokines after activation and regulate the function of innate and adaptive immune cells in antimicrobial immunity, tumor rejection and inflammatory diseases. Global transcriptional profiling has advanced our understanding of all aspects of iNKT cell biology. In this review, we discuss transcriptional analyses of iNKT cell development, functional subsets of iNKT cells, and global comparisons of iNKT cells to other innate and adaptive immune cells. Global transcriptional analysis revealed that iNKT cells have a transcriptional profile distinct from NK cells and MHC-restricted T cells, both during thymic development and in the periphery. The transcription factors EGR2 and PLZF (and microRNA like miR-150) are key regulators of the iNKT cell transcriptome during development. PLZF is one of several factors that control the homing and maintenance of organ-specific iNKT cell populations. As in MHC-restricted T cells, specific transcription factors are characteristic of functional subsets of iNKT cells, such as the transcription factor T-bet in the NKT1 subset. Exciting future directions for global transcriptional analyses include iNKT cells in disease models, diverse NKT cells and human studies.

摘要

不变自然杀伤T(iNKT)细胞是一种先天性T细胞,其表达半不变的T细胞受体(TCR),并识别由CD1d分子呈递的脂质抗原。作为固有免疫的一部分,iNKT细胞在激活后迅速产生大量细胞因子,并在抗微生物免疫、肿瘤排斥和炎症性疾病中调节固有免疫细胞和适应性免疫细胞的功能。全基因组转录谱分析推动了我们对iNKT细胞生物学各个方面的理解。在这篇综述中,我们讨论了iNKT细胞发育的转录分析、iNKT细胞的功能亚群以及iNKT细胞与其他固有免疫细胞和适应性免疫细胞的整体比较。全基因组转录分析表明,无论是在胸腺发育过程中还是在外周,iNKT细胞都具有与自然杀伤(NK)细胞和MHC限制性T细胞不同的转录谱。转录因子早期生长反应蛋白2(EGR2)和早幼粒细胞白血病锌指蛋白(PLZF,以及如miR-150这样的微小RNA)是iNKT细胞发育过程中转录组的关键调节因子。PLZF是控制器官特异性iNKT细胞群体归巢和维持的几个因子之一。与MHC限制性T细胞一样,特定的转录因子是iNKT细胞功能亚群的特征,例如NKT1亚群中的转录因子T-盒转录因子(T-bet)。全基因组转录分析令人兴奋的未来方向包括疾病模型中的iNKT细胞、不同的NKT细胞以及人类研究。

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