Unique Receptor Repertoire in Mouse Uterine NK cells

被引:113
作者
Yadi, Hakim [1 ,4 ]
Burke, Shannon [1 ,4 ]
Madeja, Zofia [2 ,4 ]
Hemberger, Myriam [2 ,4 ]
Moffett, Ashley [3 ,4 ]
Colucci, Francesco [1 ,4 ]
机构
[1] Babraham Inst, Lab Lymphocyte Signalling & Dev, Cambridge CB22 3AT, England
[2] Babraham Inst, Lab Dev Genet & Imprinting, Cambridge CB22 3AT, England
[3] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[4] Univ Cambridge, Ctr Trophoblast Res, Cambridge, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
D O I
10.4049/jimmunol.181.9.6140
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Uterine NK (uNK) cells are a prominent feature of the uterine mucosa and regulate placentation. NK cell activity is regulated by a balance of activating and inhibitory receptors, however the receptor repertoire of mouse uNK cells is unknown. We describe herein two distinct subsets of CD3(-)CD122(+) NK cells in the mouse uterus (comprising decidua and mesometrial lymphoid aggregate of pregnancy) at mid-gestation: a small subset indistinguishable from peripheral NK cells, and a larger subset that expresses NKp46 and Ly49 receptors, but not NK1.1 or DX5. This larger subset reacts with Dolichus biflores agglutinin, a marker of uNK cells in the mouse, and is adjacent to the invading trophoblast. By multiparametric analysis we show that the phenotype of uNK cells is unique and unprecedented in terms of adhesion, activation, and MHC binding potential. Thus, the Ly49 repertoire and the expression of other differentiation markers strikingly distinguish uNK cells from peripheral NK cells, suggesting that a selection process shapes the receptor repertoire of mouse uNK cells. The Journal of Immunology, 2008, 181: 6140-6147.
引用
收藏
页码:6140 / 6147
页数:8
相关论文
共 43 条
[1]   Cutting edge:: The mouse NK cell-associated antigen recognized by DX5 moncoclonal antibody is CD49b (α2 integrin, very late antigen-2) [J].
Arase, H ;
Saito, T ;
Phillips, JH ;
Lanier, LL .
JOURNAL OF IMMUNOLOGY, 2001, 167 (03) :1141-1144
[2]   Interferon γ contributes to initiation of uterine vascular modification, decidual integrity, and uterine natural killer cell maturation during normal murine pregnancy [J].
Ashkar, AA ;
Di Santo, JP ;
Croy, BA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (02) :259-269
[3]   The uterine NK cell population requires IL-15 but these cells are not required for pregnancy nor the resolution of a Listeria monocytogenes infection [J].
Barber, EM ;
Pollard, JW .
JOURNAL OF IMMUNOLOGY, 2003, 171 (01) :37-46
[4]   IL-21 induces the functional maturation of murine NK cells [J].
Brady, J ;
Hayakawa, Y ;
Smyth, MJ ;
Nutt, SL .
JOURNAL OF IMMUNOLOGY, 2004, 172 (04) :2048-2058
[5]   What does it take to make a natural killer? [J].
Colucci, F ;
Caligiuri, MA ;
Di Santo, JP .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (05) :413-425
[6]   Natural killer cell activation in mice and men: different triggers for similar weapons? [J].
Colucci, F ;
Di Santo, JP ;
Leibson, PJ .
NATURE IMMUNOLOGY, 2002, 3 (09) :807-813
[7]  
Croy BA, 2006, IMMUNOL REV, V214, P161
[8]  
DAMJANOV A, 1992, J REPROD FERTIL, V95, P679
[9]   Natural killer cell developmental pathways: A question of balance [J].
Di Santo, James P. .
ANNUAL REVIEW OF IMMUNOLOGY, 2006, 24 :257-286
[10]   Decidual NK cells regulate key developmental processes at the human fetal-maternal interface [J].
Hanna, Jacob ;
Goldman-Wohl, Debra ;
Hamani, Yaron ;
Avraham, Inbal ;
Greenfield, Caryn ;
Natanson-Yaron, Shira ;
Prus, Diana ;
Cohen-Daniel, Leonor ;
Arnon, Tal I. ;
Manaster, Irit ;
Gazit, Roi ;
Yutkin, Vladimir ;
Benharroch, Daniel ;
Porgador, Angel ;
Keshet, Eli ;
Yagel, Simcha ;
Mandelboim, Ofer .
NATURE MEDICINE, 2006, 12 (09) :1065-1074