Non-redundant functions of group 2 innate lymphoid cells

被引:68
|
作者
Jarick, Katja J. [1 ,2 ,3 ]
Topczewska, Patrycja M. [1 ,2 ,3 ]
Jakob, Manuel O. [1 ,2 ,3 ]
Yano, Hiroshi [4 ,5 ,6 ]
Arifuzzaman, Mohammad [4 ,5 ,6 ]
Gao, Xuemei [1 ,2 ,3 ]
Boulekou, Sotiria [1 ,2 ,3 ]
Stokic-Trtica, Vladislava [1 ,2 ,3 ]
Leclere, Pierre S. [1 ,2 ,3 ]
Preusser, Alexandra [1 ,2 ,3 ]
Rompe, Zoe A. [1 ,2 ,3 ]
Stamm, Anton [1 ,2 ,3 ]
Tsou, Amy M. [4 ,7 ]
Chu, Coco [4 ]
Heinrich, Frederik R. [8 ]
Guerra, Gabriela M. [8 ]
Durek, Pawel [8 ]
Ivanov, Andranik [9 ]
Beule, Dieter [9 ]
Helfrich, Sofia [1 ,2 ,3 ]
Duerr, Claudia U. [1 ,2 ,3 ]
Kuehl, Anja A. [2 ,3 ,10 ]
Stehle, Christina [2 ,8 ,11 ,12 ]
Romagnani, Chiara [2 ,8 ,11 ,12 ,13 ]
Mashreghi, Mir-Farzin [8 ]
Diefenbach, Andreas [1 ,2 ,3 ,8 ]
Artis, David [4 ,5 ,6 ,14 ]
Klose, Christoph S. N. [1 ,2 ,3 ]
机构
[1] Charite Univ Med Berlin, Dept Microbiol Infect Dis & Immunol, Berlin, Germany
[2] Free Univ Berlin, Berlin, Germany
[3] Humboldt Univ, Berlin, Germany
[4] Weill Corneall Med, Jill Roberts Inst Res Inflammatory Bower Dis, New York, NY USA
[5] Cornell Univ, Weill Cornell Med, Joan & Sanford I Weill Dept Med, Div Gastroenterol & Hepatol, New York, NY 10021 USA
[6] Cornell Univ, Weill Cornell Med, Dept Microbiol & Immunol, New York, NY 10021 USA
[7] Weill Cornell Med, Div Pediat Gastroenterol Hepatot & Nutr, New York, NY USA
[8] Inst Leibniz Assoc, Deutsch Rheuma Forschungszentrum DRFZ, Berlin, Germany
[9] Charite Univ Med Berlin, Berlin Inst Hlth, Core Unit Bioinformat, Berlin, Germany
[10] Charite Univ Med Berlin, iPATH Bertin Core Unit, Berlin, Germany
[11] Charite Univ Med Berlin, Berlin, Germany
[12] Humboldt Univ, Dept Gastroenterol Infect Dis & Rheumatol, Hindenburgdamm 30, D-12203 Berlin, Germany
[13] Leibniz Sci Campus Chron Inflammat, Berlin, Germany
[14] Cornell Univ, Weill Cornell Med, Friedman Ctr Nutr & Inflammat, Joan & Sanford I Weill Dept Med,Dept Microbiol &, New York, NY 10021 USA
基金
瑞士国家科学基金会; 欧洲研究理事会; 美国国家卫生研究院;
关键词
TRANSCRIPTION FACTOR GATA3; DIFFERENTIATION; INFLAMMATION; REDUNDANCY; EXPRESSION; PROTEINS; IMMUNITY; MICE;
D O I
10.1038/s41586-022-05395-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Protective immunity relies on the interplay of innate and adaptive immune cells with complementary and redundant functions. Innate lymphoid cells (ILCs) have recently emerged as tissue-resident, innate mirror images of the T cell system, with which they share lineage-specifying transcription factors and effector machinery(1). Located at barrier surfaces, ILCs are among the first responders against invading pathogens and thus could potentially determine the outcome of the immune response(2). However, so far it has not been possible to dissect the unique contributions of ILCs to protective immunity owing to limitations in specific targeting of ILC subsets. Thus, all of the available data have been generated either in mice lacking the adaptive immune system or with tools that also affect other immune cell subsets. In addition, it has been proposed that ILCs might be dispensable for a proper immune response because other immune cells could compensate for their absence(3-7). Here we report the generation of a mouse model based on the neuromedin U receptor 1 (Nmur1) promoter as a driver for simultaneous expression of Cre recombinase and green fluorescent protein, which enables gene targeting in group 2 ILCs (ILC2s) without affecting other innate and adaptive immune cells. Using Cre-mediated gene deletion of Id2 and Gata3 in Nmur1-expressing cells, we generated mice with a selective and specific deficiency in ILC2s. ILC2-deficient mice have decreased eosinophil counts at steady state and are unable to recruit eosinophils to the airways in models of allergic asthma. Further, ILC2-deficient mice do not mount an appropriate immune and epithelial type 2 response, resulting in a profound defect in worm expulsion and a non-protective type 3 immune response. In total, our data establish non-redundant functions for ILC2s in the presence of adaptive immune cells at steady state and during disease and argue for a multilayered organization of the immune system on the basis of a spatiotemporal division of labour.
引用
收藏
页码:794 / +
页数:30
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