Current overview of the role of neuropeptides in ILC2s and future directions

被引:8
作者
Irie, Misato [1 ]
Sasahara, Kotaro [1 ]
Artis, David [2 ,3 ]
Kabata, Hiroki [1 ]
机构
[1] Keio Univ, Sch Med, Dept Med, Div Pulm Med, Shinanomachi 35,Shinjuku Ku, Tokyo 1608582, Japan
[2] Cornell Univ, Jill Roberts Inst Res Inflammatory Bowel Dis, Div Gastroenterol & Hepatol,Weill Cornell Med, Joan & Sanford I Weill Dept Med,Dept Microbiol &, New York, NY 10021 USA
[3] Cornell Univ, Weill Cornell Med, Friedman Ctr Nutr & Inflammat, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
Group 2 innate lymphoid cells; IL-33; Neuro-immune interactions; Neurons Type 2 inflammation; INNATE LYMPHOID-CELLS; NEGATIVE REGULATION; MECHANISMS;
D O I
10.1016/j.alit.2022.03.002
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
The neural and immune systems are closely connected, and recently, their molecular mechanisms and relationships with diseases have attracted substantial attention. Particularly, it has been increasingly reported that ILC2s, which produce type 2 cytokines independent of acquired immunity, are regulated by neuropeptides such as catecholamines, acetylcholine, vasoactive intestinal peptide, neuromedins, and calcitonin gene-related peptide. However, the regulatory mechanisms in this regard are only partially understood, implying that further studies are still needed to clarify the complete mechanisms and processes. In this review, we summarize current reports on the regulatory effect of neuropeptides on ILC2s, some of which have conflicting results, possibly owing to the complexity of G-protein coupled receptors. By summarizing the current evidence, we hope to be able to identify what is currently unknown as well as what needs to be clarified in the future. Copyright (c) 2022, Japanese Society of Allergology. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:294 / 300
页数:7
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