作者
Anne-Laure Flamar, Christoph SN Klose, Jesper B Moeller, Tanel Mahlakõiv, Nicholas J Bessman, Wen Zhang, Saya Moriyama, Vladislava Stokic-Trtica, Lucille C Rankin, Gregory Garbès Putzel, Hans-Reimer Rodewald, Zhengxiang He, Lili Chen, Sergio A Lira, Gerard Karsenty, David Artis
发表日期
2020/4/14
期刊
Immunity
卷号
52
期号
4
页码范围
606-619. e6
出版商
Elsevier
简介
Group 2 innate lymphoid cells (ILC2s) regulate immunity, inflammation, and tissue homeostasis. Two distinct subsets of ILC2s have been described: steady-state natural ILC2s and inflammatory ILC2s, which are elicited following helminth infection. However, how tissue-specific cues regulate these two subsets of ILC2s and their effector functions remains elusive. Here, we report that interleukin-33 (IL-33) promotes the generation of inflammatory ILC2s (ILC2INFLAM) via induction of the enzyme tryptophan hydroxylase 1 (Tph1). Tph1 expression was upregulated in ILC2s upon activation with IL-33 or following helminth infection in an IL-33-dependent manner. Conditional deletion of Tph1 in lymphocytes resulted in selective impairment of ILC2INFLAM responses and increased susceptibility to helminth infection. Further, RNA sequencing analysis revealed altered gene expression in Tph1 deficient ILC2s including …
引用总数
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