Volume 181, Issue 1 pp. 149-157

Rat natural killer cell receptor systems and recognition of MHC class I molecules

Bent Rolstad

Corresponding Author

Bent Rolstad

Department of Anatomy, Institute of Basic Medical Sciences, University of Oslo, Blindern, Oslo, Norway

Correspondence to: Bent Rolstad
Department of Anatomy
Institute of Basic Medical Sciences
University of Oslo
P.O. Box 1105 Blindern
N-0317 Oslo
Norway
Fax: 47 22851278
e-mail: [email protected]Search for more papers by this author
Christian Naper

Christian Naper

Department of Anatomy, Institute of Basic Medical Sciences, University of Oslo, Blindern, Oslo, Norway

Immunology/Arthritis Section, Veterans Administration Medical Center, University of California, San Francisco, San Francisco, California, USA

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Guro Løvik

Guro Løvik

Department of Anatomy, Institute of Basic Medical Sciences, University of Oslo, Blindern, Oslo, Norway

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John Torgils Vaage

John Torgils Vaage

Department of Anatomy, Institute of Basic Medical Sciences, University of Oslo, Blindern, Oslo, Norway

Institute of Immunology, Rikshospitalet, The University Hospital of Oslo, Oslo, Norway

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James C. Ryan

James C. Ryan

Immunology/Arthritis Section, Veterans Administration Medical Center, University of California, San Francisco, San Francisco, California, USA

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Eva Bäckman-Petersson

Eva Bäckman-Petersson

Department of Immunology, The Babraham Institute, Babraham Hall, Cambridge UK

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Ralf D. Kirsch

Ralf D. Kirsch

Department of Immunology, The Babraham Institute, Babraham Hall, Cambridge UK

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Geoffrey W. Butcher

Geoffrey W. Butcher

Department of Immunology, The Babraham Institute, Babraham Hall, Cambridge UK

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First published: 04 January 2002
Citations: 30

Abstract

Summary: Rat natural killer (NK) cells recognize MHC-I molecules encoded by both the classical (RT1-A) and non-classical (RT1-C/E/M) MHC class I (MHC-I) regions. We have identified a receptor, the STOK2 antigen, which belongs to the Ly-49 family of killer cell lectin-like receptors, and we have localized the gene encoding it to the rat natural killer cell gene complex. We have also shown that it inhibits NK cytotoxicity when recognizing its cognate MHC-I ligand RT1-A1c on a target cell. This is the first inhibitory Ly-49–MHC-I interaction identified in the rat and highlights the great similarity between rat and mouse Ly-49 receptors and their MHC ligands. However, the mode of rat NK-cell recognition of target cells indicates that positive recognition of allo-MHC determinants, especially those encoded by the RT1-C/E/M region, is a prevalent feature. NK cells recruited to the peritoneum as a consequence of alloimmunization display positive recognition of allodeterminants. In one case, NK cells activated in this way have been shown to be specific for the immunizing, non-classical class I molecule RT1-Eu. These findings show that allospecific NK cells sometimes show features reminiscent of the adaptive immune response.

This research was supported by grants from the Norwegian Cancer Society, the Research Council of Norway, the Anders Jahre's Fund, the UK BBSRC to RDK (PhD studentship) and GWB (Competitive Strategic Grant). EBP also acknowledges support from The Swedish Foundation for International Cooperation in Research and Higher Education, The Knut and Alice Wallenberg Foundation and the Swedish Institute.

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