Literature DB >> 10556824

MHC class Ia molecules alone control NK-mediated bone marrow graft rejection.

K Grigoriadou1, C Ménard, B Pérarnau, F A Lemonnier.   

Abstract

Mice with functionally deleted genes encoding MHC class I heavy (H-2K(b), H-2D(b)) and light (beta2-microglobulin) chains were used in bone marrow cell transfer experiments to study the role of class Ia and Ib molecules in NK cell function. Absence of H-2K(b) and absence of H-2D(b) on bone marrow cells resulted in complete and in almost complete NK-mediated rejection, respectively. Absence of either H-2 class Ib (at least when expressed in H-2 class Ia-deficient mice) or cell surface class Ia free heavy chains did not result in bone marrow rejection. Thus, in C57BL/6 adult mice, the inactivation of NK cells required for bone marrow cell engraftment relies entirely upon-H-2 class Ia molecules. These results imply the existence of an inhibitory receptor which recognizes either directly or indirectly H-2D(b) molecules and further suggest that in C57BL/6 mice the NK cells which do not express a H-2K(b) specific inhibitory receptor necessarily express an H-2D(b)-specific one.

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Year:  1999        PMID: 10556824     DOI: 10.1002/(SICI)1521-4141(199911)29:11<3683::AID-IMMU3683>3.0.CO;2-B

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  8 in total

1.  A subset of natural killer cells achieves self-tolerance without expressing inhibitory receptors specific for self-MHC molecules.

Authors:  Nadine C Fernandez; Emmanuel Treiner; Russell E Vance; Amanda M Jamieson; Suzanne Lemieux; David H Raulet
Journal:  Blood       Date:  2005-02-22       Impact factor: 22.113

2.  Mouse NK cell-mediated rejection of bone marrow allografts exhibits patterns consistent with Ly49 subset licensing.

Authors:  Kai Sun; Maite Alvarez; Erik Ames; Isabel Barao; Mingyi Chen; Dan L Longo; Doug Redelman; William J Murphy
Journal:  Blood       Date:  2011-12-19       Impact factor: 22.113

3.  HLA-A*01:03, HLA-A*24:02, HLA-B*08:01, HLA-B*27:05, HLA-B*35:01, HLA-B*44:02, and HLA-C*07:01 monochain transgenic/H-2 class I null mice: novel versatile preclinical models of human T cell responses.

Authors:  Rachid Boucherma; Hédia Kridane-Miledi; Romain Bouziat; Michael Rasmussen; Tanja Gatard; Francina Langa-Vives; Brigitte Lemercier; Annick Lim; Marion Bérard; Lbachir Benmohamed; Søren Buus; Ronald Rooke; François A Lemonnier
Journal:  J Immunol       Date:  2013-06-17       Impact factor: 5.422

4.  HLA reduces killer cell Ig-like receptor expression level and frequency in a humanized mouse model.

Authors:  Jeroen van Bergen; Allan Thompson; Melissa van Pel; Christelle Retière; Daniela Salvatori; David H Raulet; John Trowsdale; Frits Koning
Journal:  J Immunol       Date:  2013-02-06       Impact factor: 5.422

5.  Cutting edge: viral infection breaks NK cell tolerance to "missing self".

Authors:  Joseph C Sun; Lewis L Lanier
Journal:  J Immunol       Date:  2008-12-01       Impact factor: 5.422

6.  Distinct KIR/HLA compound genotypes affect the kinetics of human antiviral natural killer cell responses.

Authors:  Golo Ahlenstiel; Maureen P Martin; Xiaojiang Gao; Mary Carrington; Barbara Rehermann
Journal:  J Clin Invest       Date:  2008-03       Impact factor: 14.808

Review 7.  Regulation of NK cell responsiveness to achieve self-tolerance and maximal responses to diseased target cells.

Authors:  Nathalie T Joncker; David H Raulet
Journal:  Immunol Rev       Date:  2008-08       Impact factor: 12.988

8.  Natural killer cell education in mice with single or multiple major histocompatibility complex class I molecules.

Authors:  Sofia Johansson; Maria Johansson; Eleftheria Rosmaraki; Gustaf Vahlne; Ramit Mehr; Mali Salmon-Divon; François Lemonnier; Klas Kärre; Petter Höglund
Journal:  J Exp Med       Date:  2005-04-04       Impact factor: 14.307

  8 in total

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