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The Journal of Immunology, 2008, 181, 6140 -6147
Copyright © 2008 by The American Association of Immunologists, Inc.

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Unique Receptor Repertoire in Mouse Uterine NK cells1

Hakim Yadi*,§, Shannon Burke*,§, Zofia Madeja{dagger},§, Myriam Hemberger{dagger},§, Ashley Moffett{ddagger},§ and Francesco Colucci2,*,§

* Laboratory of Lymphocyte Signalling and Development and {dagger} Laboratory of Developmental Genetics and Imprinting, The Babraham Institute, Cambridge, United Kingdom; and {ddagger} Department of Pathology, and § Centre for Trophoblast Research, University of Cambridge, Cambridge, United Kingdom

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 CD3CD122+ 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 costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

1 This work was supported by grants to F.C. from the Medical Research Council, United Kingdom, and a Babraham Institute Synergy Grant to M.H. and F.C.

2 Address correspondence and reprint requests to Dr. Francesco Colucci, Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, CB22 3AT, Cambridge, United Kingdom. E-mail address: francesco.colucci{at}bbsrc.ac.uk

3 Abbreviations used in this paper: uNK, uterine NK; DAPI, 4',6-diamidino-2-phenylindole; gd, gestation day; DBA, Dolichos biflores agglutinin; Lin, lineage; MLAp, mesometrial lymphoid aggregate of pregnancy; PAS, periodic acid-Schiff.




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