Division of Biology, University of California San Diego, La Jolla, CA 92093.
J Immunol. 2014 Mar 1;192(5):2227-36. doi: 10.4049/jimmunol.1302904. Epub 2014 Jan 27.
Disease outcome is known to be influenced by defined subsets of invariant NKT (iNKT) cells residing in distinct locations within peripheral tissue. However, the factors governing the development of these unique iNKT sublineages during thymic development are unknown. In this study we explored the mechanism by which E protein transcription factors and their negative regulators, the Id proteins, control the development of iNKT sublineages after positive selection. We found that E proteins directly bound the promyelocytic leukemia zinc finger (PLZF) promoter and were required for expression of this lineage-defining transcription factor and for the maturation and expansion of thymic iNKT cells. Moreover, expression of the negative regulators of E proteins, Id2 and Id3, defined distinct iNKT cell sublineages. Id3 was expressed in PLZF(high) NKT2 cells and loss of Id3 allowed for increased thymic iNKT cell expansion and abundance of the PLZF(+) NKT2 sublineage. Id2 was expressed in T-BET(+) NKT1 cells, and both Id proteins were required for the formation of this sublineage. Thus, we provide insight into E and Id protein regulation of iNKT cell proliferation and differentiation to specific sublineages during development in the thymus.
疾病的转归已知受到外周组织中不同位置的固有自然杀伤 T(iNKT)细胞特定亚群的影响。然而,在胸腺发育过程中,决定这些独特 iNKT 亚群发育的因素尚不清楚。在这项研究中,我们探讨了 E 蛋白转录因子及其负调控因子 ID 蛋白在阳性选择后控制 iNKT 亚群发育的机制。我们发现 E 蛋白直接结合早幼粒细胞白血病锌指(PLZF)启动子,对于该谱系定义转录因子的表达以及胸腺 iNKT 细胞的成熟和扩增是必需的。此外,E 蛋白负调控因子 ID2 和 ID3 的表达定义了不同的 iNKT 细胞亚群。ID3 在 PLZF(high)NKT2 细胞中表达,ID3 的缺失允许胸腺 iNKT 细胞的扩增增加和 PLZF(+)NKT2 亚群的丰度增加。ID2 在 T-BET(+)NKT1 细胞中表达,这两种 ID 蛋白对于该亚群的形成都是必需的。因此,我们提供了在胸腺发育过程中 E 和 ID 蛋白对 iNKT 细胞增殖和分化为特定亚群的调控的深入了解。