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

被引:106
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
[1]   Functional interactions between dendritic cells and NK cells during viral infection [J].
Andrews, DM ;
Scalzo, AA ;
Yokoyama, WM ;
Smyth, MJ ;
Degli-Esposti, MA .
NATURE IMMUNOLOGY, 2003, 4 (02) :175-181
[2]   MOUSE NK1(+) T-CELLS [J].
BENDELAC, A .
CURRENT OPINION IN IMMUNOLOGY, 1995, 7 (03) :367-374
[3]   The biology of NKT cells [J].
Bendelac, Albert ;
Savage, Paul B. ;
Teyton, Luc .
ANNUAL REVIEW OF IMMUNOLOGY, 2007, 25 :297-336
[4]   Invariant natural killer T cells recognize lipid self antigen induced by microbial danger signals [J].
Brennan, Patrick J. ;
Tatituri, Raju V. V. ;
Brigl, Manfred ;
Kim, Edy Y. ;
Tuli, Amit ;
Sanderson, Joseph P. ;
Gadola, Stephan D. ;
Hsu, Fong-Fu ;
Besra, Gurdyal S. ;
Brenner, Michael B. .
NATURE IMMUNOLOGY, 2011, 12 (12) :1202-U97
[5]   Mechanism of CD1d-restricted natural killer T cell activation during microbial infection [J].
Brigl, M ;
Bry, L ;
Kent, SC ;
Gumperz, JE ;
Brenner, MB .
NATURE IMMUNOLOGY, 2003, 4 (12) :1230-1237
[6]   Innate and cytokine-driven signals, rather than microbial antigens, dominate in natural killer T cell activation during microbial infection [J].
Brigl, Manfred ;
Tatituri, Raju V. V. ;
Watts, Gerald F. M. ;
Bhowruth, Veemal ;
Leadbetter, Elizabeth A. ;
Barton, Nathaniel ;
Cohen, Nadia R. ;
Hsu, Fong-Fu ;
Besra, Gurdyal S. ;
Brenner, Michael B. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2011, 208 (06) :1163-1177
[7]   How invariant natural killer T cells respond to infection by recognizing microbial or endogenous lipid antigens [J].
Brigl, Manfred ;
Brenner, Michael B. .
SEMINARS IN IMMUNOLOGY, 2010, 22 (02) :79-86
[8]   Harnessing invariant NKT cells in vaccination strategies [J].
Cerundolo, Vincenzo ;
Silk, Jonathan D. ;
Masri, S. Hajar ;
Salio, Mariolina .
NATURE REVIEWS IMMUNOLOGY, 2009, 9 (01) :28-38
[9]   Antigen Presentation by CD1: Lipids, T Cells, and NKT Celts in Microbial Immunity [J].
Cohen, Nadia R. ;
Garg, Salil ;
Brenner, Michael B. .
ADVANCES IN IMMUNOLOGY, VOL 102, 2009, 102 :1-94
[10]   In vivo evidence for a dependence on interleukin 15 for survival of natural killer cells [J].
Cooper, MA ;
Bush, JE ;
Fehniger, TA ;
VanDeusen, JB ;
Waite, RE ;
Liu, Y ;
Aguila, HL ;
Caligiuri, MA .
BLOOD, 2002, 100 (10) :3633-3638