Cutting Edge: Notch Signaling Promotes the Plasticity of Group-2 Innate Lymphoid Cells

被引:105
作者
Zhang, Kangning [1 ]
Xu, Xingyuan [1 ,2 ]
Pasha, Muhammad Asghar [3 ]
Siebel, Christian W. [4 ]
Costello, Angelica [1 ]
Haczku, Angela [5 ]
MacNamara, Katherine [1 ]
Liang, Tingbo [2 ]
Zhu, Jinfang [6 ]
Bhandoola, Avinash [7 ]
Maillard, Ivan [8 ,9 ]
Yang, Qi [1 ]
机构
[1] Albany Med Coll, Dept Immunol & Microbial Dis, 47 New Scotland Ave,MC-151, Albany, NY 12208 USA
[2] Zhejiang Univ, Dept Hepatobiliary & Pancreat Surg, Affiliated Hosp 2, Hangzhou 310009, Zhejiang, Peoples R China
[3] Albany Med Coll, Dept Med, Div Allergy & Immunol, Albany, NY 12203 USA
[4] Genentech Inc, Dept Discovery Oncol, San Francisco, CA 94080 USA
[5] Univ Calif Davis, Div Pulm Crit Care & Sleep Med, Dept Internal Med, Translat Lung Biol Ctr, Davis, CA 95616 USA
[6] NIAID, Mol & Cellular Immunoregulat Unit, Immunol Lab, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[7] NCI, T Cell Biol & Dev Unit, Lab Genome Integr, Ctr Canc Res,NIH, Bethesda, MD 20892 USA
[8] Univ Michigan, Inst Life Sci, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
[9] Univ Michigan, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
FUNCTIONAL PLASTICITY; LYMPHOCYTES; EXPRESSION;
D O I
10.4049/jimmunol.1601421
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The mechanisms underlying lymphocyte lineage stabil-ity and plasticity remain elusive. Recent work indicates that innate lymphoid cells (ILC) possess substantial plasticity. Whereas natural ILC2 (nILC2) produce type-2 cytokines, plastic inflammatory ILC2 (iILC2) can coproduce both type-2 cytokines and the ILC3-characteristic cytokine, IL-17. Mechanisms that elicit this lineage plasticity, and the importance in health and disease, remain unclear. In this study we show that iILC2 are potent inducers of airway inflammation in response to acute house dust mite challenge. We find that Notch signaling induces lineage plasticity of ma-ture ILC2 and drives the conversion of nILC2 into iILC2. Acute blockade of Notch signaling abolished functional iILC2, but not nILC2, in vivo. Exposure of isolated nILC2 to Notch ligands induced Rorc ex-pression and elicited dual IL-13/ IL-17 production, con-verting nILC2 into iILC2. Together these results reveal a novel role for Notch signaling in eliciting ILC2 plasticity and driving the emergence of highly proinflammatory innate lymphocytes.
引用
收藏
页码:1798 / 1803
页数:6
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