Shared and distinct transcriptional programs underlie the hybrid nature of iNKT cells

被引:110
作者
Cohen, Nadia R. [1 ]
Brennan, Patrick J. [1 ]
Shay, Tal [2 ]
Watts, Gerald F. [1 ]
Brigl, Manfred [1 ,3 ]
Kang, Joonsoo [4 ]
Brenner, Michael B. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med,Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
[2] Broad Inst MIT & Harvard, Cambridge, MA USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Pathol, Boston, MA 02115 USA
[4] Univ Massachusetts, Sch Med, Dept Pathol, Worcester, MA 01605 USA
基金
美国国家卫生研究院;
关键词
INVARIANT NKT CELLS; KILLER T-CELLS; INTRAEPITHELIAL LYMPHOCYTES; GENE-EXPRESSION; DENDRITIC CELLS; MICROBIAL INFECTION; TERMINAL MATURATION; EFFECTOR FUNCTIONS; IMMUNE-RESPONSES; VIRAL-INFECTION;
D O I
10.1038/ni.2490
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Invariant natural killer T cells (iNKT cells) are innate-like T lymphocytes that act as critical regulators of the immune response. To better characterize this population, we profiled gene expression in iNKT cells during ontogeny and in peripheral subsets as part of the Immunological Genome Project. High-resolution comparative transcriptional analyses defined developmental and subset-specific programs of gene expression by iNKT cells. In addition, we found that iNKT cells shared an extensive transcriptional program with NK cells, similar in magnitude to that shared with major histocompatibility complex (MHC)-restricted T cells. Notably, the program shared by NK cells and iNKT cells also operated constitutively in gamma delta T cells and in adaptive T cells after activation. Together our findings highlight a core effector program regulated distinctly in innate and adaptive lymphocytes.
引用
收藏
页码:90 / 99
页数:10
相关论文
共 56 条
[31]   Regulation of NKT cells by Ly49: Analysis of primary NKT cells and generation of NKT cell line [J].
Maeda, M ;
Lohwasser, S ;
Yamamura, T ;
Takei, F .
JOURNAL OF IMMUNOLOGY, 2001, 167 (08) :4180-4186
[32]   PREDOMINANT EXPRESSION OF INVARIANT V(ALPHA)14(+) TCR ALPHA-CHAIN IN NK1.1(+) T-CELL POPULATIONS [J].
MAKINO, Y ;
KANNO, R ;
ITO, T ;
HIGASHINO, K ;
TANIGUCHI, M .
INTERNATIONAL IMMUNOLOGY, 1995, 7 (07) :1157-1161
[33]   Differential Expression of Ly6C and T-bet Distinguish Effector and Memory Th1 CD4+ Cell Properties during Viral Infection [J].
Marshall, Heather D. ;
Chandele, Anmol ;
Jung, Yong Woo ;
Meng, Hailong ;
Poholek, Amanda C. ;
Parish, Ian A. ;
Rutishauser, Rachel ;
Cui, Weiguo ;
Kleinstein, Steven H. ;
Craft, Joe ;
Kaech, Susan M. .
IMMUNITY, 2011, 35 (04) :633-646
[34]   Tracking the response of natural killer T cells to a glycolipid antigen using CD1d tetramers [J].
Matsuda, JL ;
Naidenko, OV ;
Gapin, L ;
Nakayama, T ;
Taniguchi, M ;
Wang, CR ;
Koezuka, Y ;
Kronenberg, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (05) :741-753
[35]   T-bet concomitantly controls migration, survival, and effector functions during the development of Vα14i NKT cells [J].
Matsuda, JL ;
Zhang, QJ ;
Ndonye, R ;
Richardson, SK ;
Howell, AR ;
Gapin, L .
BLOOD, 2006, 107 (07) :2797-2805
[36]   Homeostasis of Vα14i NKT cells [J].
Matsuda, JL ;
Gapin, L ;
Sidobre, S ;
Kieper, WC ;
Tan, JYT ;
Ceredig, R ;
Surh, CD ;
Kronenberg, M .
NATURE IMMUNOLOGY, 2002, 3 (10) :966-974
[37]   The Role of the Basic Helix-Loop-Helix Transcription Factor Dec1 in the Regulatory T Cells [J].
Miyazaki, Kazuko ;
Miyazaki, Masaki ;
Guo, Yun ;
Yamasaki, Norimasa ;
Kanno, Masamoto ;
Honda, Zen-ichiro ;
Oda, Hideaki ;
Kawamoto, Hiroshi ;
Honda, Hiroaki .
JOURNAL OF IMMUNOLOGY, 2010, 185 (12) :7330-7339
[38]   γδ T cell subsets: A link between TCR and function? [J].
O'Brien, Rebecca L. ;
Born, Willi K. .
SEMINARS IN IMMUNOLOGY, 2010, 22 (04) :193-198
[39]   IFN-γ-mediated negative feedback regulation of NKT-cell function by CD94/NKG2 [J].
Ota, T ;
Takeda, K ;
Akiba, H ;
Hayakawa, Y ;
Ogasawara, K ;
Ikarashi, Y ;
Miyake, S ;
Wakasugi, H ;
Yamamura, T ;
Kronenberg, M ;
Raulet, DH ;
Kinoshita, K ;
Yagita, H ;
Smyth, MJ ;
Okumura, K .
BLOOD, 2005, 106 (01) :184-192
[40]   Activation of invariant NKT cells by toll-like receptor 9-stimulated dendritic cells requires type I interferon and charged Glycosphingolipids [J].
Paget, Christophe ;
Mallevaey, Thierry ;
Speak, Anneliese O. ;
Torres, David ;
Fontaine, Josette ;
Sheehan, Kathleen C. F. ;
Capron, Monique ;
Ryffel, Bernhard ;
Faveeuw, Christelle ;
de Moraes, Maria Leite ;
Platt, Frances ;
Trottein, Francois .
IMMUNITY, 2007, 27 (04) :597-609