自然杀伤性T细胞
生物
细胞生物学
效应器
颗粒酶B
细胞分化
抑制因子
干扰素
T细胞
转录因子
免疫学
免疫系统
基因
遗传学
作者
Klaas P. J. M. van Gisbergen,Natasja A. M. Kragten,Kirsten M. L. Hertoghs,Felix M. Wensveen,Stipan Jonjić,Jörg Hamann,Martijn A. Nolte,René A. W. van Lier
摘要
The transcriptional repressor Blimp-1 mediates the terminal differentiation of many cell types, including T cells. Here we identified Hobit (Znf683) as a previously unrecognized homolog of Blimp-1 that was specifically expressed in mouse natural killer T cells (NKT cells). Through studies of Hobit-deficient mice, we found that Hobit was essential for the formation of mature thymic NKT cells. In the periphery, Hobit repressed the accumulation of interferon-γ (IFN-γ)-producing NK1.1(lo) NKT cells at steady state. After antigenic stimulation, Hobit repressed IFN-γ expression, whereas after innate stimulation, Hobit induced granzyme B expression. Thus, reminiscent of the function of Blimp-1 in other lymphocytes, Hobit controlled the maintenance of quiescent, fully differentiated NKT cells and regulated their immediate effector functions.
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