Transcription factor RORα is critical for nuocyte development

被引:469
作者
Wong, See Heng [1 ]
Walker, Jennifer A. [1 ]
Jolin, Helen E. [1 ]
Drynan, Lesley F. [1 ]
Hams, Emily [2 ]
Camelo, Ana [1 ]
Barlow, Jillian L. [1 ]
Neill, Daniel R. [1 ]
Panova, Veera [1 ]
Koch, Ute
Radtke, Freddy [3 ]
Hardman, Clare S. [1 ]
Hwang, You Yi [1 ]
Fallon, Padraic G. [2 ,4 ,5 ]
McKenzie, Andrew N. J. [1 ]
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[2] Trinity Coll Dublin, Inst Mol Med, Sch Med, Dublin, Ireland
[3] Ecole Polytech Fed Lausanne, Inst Suisse Rech Expt Canc, Lausanne, Switzerland
[4] Trinity Coll Dublin, Trinity Biomed Sci Inst, Sch Med, Dublin, Ireland
[5] Our Ladys Childrens Hosp, Natl Childrens Res Ctr, Dublin, Ireland
基金
爱尔兰科学基金会; 英国医学研究理事会;
关键词
INNATE LYMPHOID-CELLS; DELTA-LIKE; 4; T-CELLS; GAMMA-T; DENDRITIC CELLS; RECEPTOR-ALPHA; STEM-CELLS; NOTCH; DIFFERENTIATION; IL-4;
D O I
10.1038/ni.2208
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nuocytes are essential in innate type 2 immunity and contribute to the exacerbation of asthma responses. Here we found that nuocytes arose in the bone marrow and differentiated from common lymphoid progenitors, which indicates they are distinct, previously unknown members of the lymphoid lineage. Nuocytes required interleukin 7 (IL-7), IL-33 and Notch signaling for development in vitro. Pro-T cell progenitors at double-negative stage 1 (DN1) and DN2 maintained nuocyte potential in vitro, although the thymus was not essential for nuocyte development. Notably, the transcription factor ROR alpha was critical for the development of nuocytes and their role in the expulsion of parasitic worms.
引用
收藏
页码:229 / U43
页数:9
相关论文
共 50 条
[1]   Instruction of distinct CD4 T helper cell fates by different notch ligands on antigen-presenting cells [J].
Amsen, D ;
Blander, JM ;
Lee, GR ;
Tanigaki, K ;
Honjo, T ;
Flavell, RA .
CELL, 2004, 117 (04) :515-526
[2]   Interleukin 25 promotes the initiation of proallergic type 2 responses [J].
Angkasekwinai, Pornpimon ;
Park, Heon ;
Wang, Yui-Hsi ;
Wang, Yi-Hong ;
Chang, Seon Hee ;
Corry, David B. ;
Liu, Yong-Jun ;
Zhu, Zhou ;
Dong, Chen .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (07) :1509-1517
[3]   Innate IL-13-producing nuocytes arise during allergic lung inflammation and contribute to airways hyperreactivity [J].
Barlow, Jillian L. ;
Bellosi, Agustin ;
Hardman, Clare S. ;
Drynan, Lesley F. ;
Wong, See Heng ;
Cruickshank, James P. ;
McKenzie, Andrew N. J. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2012, 129 (01) :191-U275
[4]   Innate lymphoid cells drive interleukin-23-dependent innate intestinal pathology [J].
Buonocore, Sofia ;
Ahern, Philip P. ;
Uhlig, Holm H. ;
Ivanov, Ivaylo I. ;
Littman, Dan R. ;
Maloy, Kevin J. ;
Powrie, Fiona .
NATURE, 2010, 464 (7293) :1371-1375
[5]   A human natural killer cell subset provides an innate source of IL-22 for mucosal immunity [J].
Cella, Marina ;
Fuchs, Anja ;
Vermi, William ;
Facchetti, Fabio ;
Otero, Karel ;
Lennerz, Jochen K. M. ;
Doherty, Jason M. ;
Mills, Jason C. ;
Colonna, Marco .
NATURE, 2009, 457 (7230) :722-725
[6]   Innate lymphoid cells mediate influenza-induced airway hyper-reactivity independently of adaptive immunity [J].
Chang, Ya-Jen ;
Kim, Hye Young ;
Albacker, Lee A. ;
Baumgarth, Nicole ;
McKenzie, Andrew N. J. ;
Smith, Dirk E. ;
DeKruyff, Rosemarie H. ;
Umetsu, Dale T. .
NATURE IMMUNOLOGY, 2011, 12 (07) :631-U186
[7]   Human fetal lymphoid tissue-inducer cells are interleukin 17-producing precursors to RORC+ CD127+ natural killer-like cells [J].
Cupedo, Tom ;
Crellin, Natasha K. ;
Papazian, Natalie ;
Rombouts, Elwin J. ;
Weijer, Kees ;
Grogan, Jane L. ;
Fibbe, Willem E. ;
Cornelissen, Jan J. ;
Spits, Hergen .
NATURE IMMUNOLOGY, 2009, 10 (01) :66-74
[8]   Lymphocyte development and function in the absence of retinoic acid-related orphan receptor α [J].
Dzhagalov, I ;
Giguère, V ;
He, YW .
JOURNAL OF IMMUNOLOGY, 2004, 173 (05) :2952-2959
[9]   Identification of an interleukin (IL)-25-dependent cell population that provides IL-4, IL-5, and IL-13 at the onset of helminth expulsion [J].
Fallon, PG ;
Ballantyne, SJ ;
Mangan, NE ;
Barlow, JL ;
Dasvarma, A ;
Hewett, DR ;
McIlgorm, A ;
Jolin, HE ;
McKenzie, ANJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (04) :1105-1116
[10]   IL-4 induces characteristic Th2 responses even in the combined absence of IL-5, IL-9, and IL-13 [J].
Fallon, PG ;
Jolin, HE ;
Smith, P ;
Emson, CL ;
Townsend, MJ ;
Fallon, R ;
Smith, P ;
McKenzie, ANJ .
IMMUNITY, 2002, 17 (01) :7-17