先天性淋巴细胞
先天免疫系统
生物
免疫学
乙酰胆碱
免疫系统
淋巴系统
免疫
淋巴细胞生成
蠕虫
细胞生物学
内分泌学
干细胞
造血
作者
Luke B. Roberts,Corinna Schnoeller,Rita Berkachy,Matthew Darby,Jamie Pillaye,Menno J. Oudhoff,N. Parmar,Claire Mackowiak,Delphine Sedda,Valérie Quesniaux,Bernhard Ryffel,Vaux Rachel,Kleoniki Gounaris,Sylvie Berrard,David R. Withers,William Horsnell,Murray E. Selkirk
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2021-03-04
卷期号:6 (57)
被引量:89
标识
DOI:10.1126/sciimmunol.abd0359
摘要
Innate lymphoid cells (ILCs) are critical mediators of immunological and physiological responses at mucosal barrier sites. Whereas neurotransmitters can stimulate ILCs, the synthesis of small-molecule neurotransmitters by these cells has only recently been appreciated. Group 2 ILCs (ILC2s) are shown here to synthesize and release acetylcholine (ACh) during parasitic nematode infection. The cholinergic phenotype of pulmonary ILC2s was associated with their activation state, could be induced by in vivo exposure to extracts of Alternaria alternata or the alarmin cytokines interleukin-33 (IL-33) and IL-25, and was augmented by IL-2 in vitro. Genetic disruption of ACh synthesis by murine ILC2s resulted in increased parasite burdens, lower numbers of ILC2s, and reduced lung and gut barrier responses to Nippostrongylus brasiliensis infection. These data demonstrate a functional role for ILC2-derived ACh in the expansion of ILC2s for maximal induction of type 2 immunity.
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