先天性淋巴细胞
关贸总协定3
生物
免疫学
转录因子
先天免疫系统
白细胞介素33
花粉热
胸腺基质淋巴细胞生成素
细胞因子
细胞生物学
关贸总协定
抄写(语言学)
RAR相关孤儿受体γ
GATA转录因子
增强子
转录调控
锌指
基因
免疫系统
白细胞介素
过敏
遗传学
作者
Jenny Mjösberg,Jochem H. Bernink,Korneliusz Golebski,Julien J. Karrich,Charlotte P. Peters,Bianca Blom,Anje A. te Velde,Wytske J. Fokkens,Cornelis M. van Drunen,Hergen Spits
出处
期刊:Immunity
[Elsevier]
日期:2012-10-01
卷期号:37 (4): 649-659
被引量:553
标识
DOI:10.1016/j.immuni.2012.08.015
摘要
Type 2 innate lymphoid cells (ILC2s) are part of a large family of ILCs that are important effectors in innate immunity, lymphoid organogenesis, and tissue remodeling. ILC2s mediate parasite expulsion but also contribute to airway inflammation, emphasizing the functional similarity between these cells and Th2 cells. Consistent with this, we report that the transcription factor GATA3 was highly expressed by human ILC2s. CRTH2(+) ILC2s were enriched in nasal polyps of patients with chronic rhinosinusitis, a typical type 2-mediated disease. Nasal polyp epithelial cells expressed TSLP, which enhanced STAT5 activation, GATA3 expression, and type 2 cytokine production in ILC2s. Ectopic expression of GATA3 in Lin(-)CD127(+)CRTH2(-) cells resulted in induction of CRTH2 and the capacity to produce high amounts of type 2 cytokines in response to TSLP plus IL-33. Hence, we identify GATA3, potently regulated by TSLP, as an essential transcription factor for the function of human ILC2s.
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