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Blood, 1 August 2004, Vol. 104, No. 3, pp. 781-783.
Prepublished online as a Blood First Edition Paper on April 6, 2004; DOI 10.1182/blood-2003-10-3468.


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Submitted October 10, 2003
Accepted March 22, 2004

Role of a NK receptor, KLRE-1, in bone marrow allograft rejection: analysis with KLRE-1 deficient mice

Eiko Shimizu, Junzo Koike, Hiroshi Wakao, Ken-ichiro Seino, Haruhiko Koseki, Terutaka Kakiuchi, Toshinori Nakayama*, and Masaru Taniguchi

Molecular Immunology, Chiba University Graduate School of Medicine, Chiba, Chiba, Japan
Laboratory for Immune Regulation, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa, Japan
Molecular Embryology, Chiba University Graduate School of Medicine, Chiba, Chiba, Japan; Laboratory for Developmental Genetics, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa, Japan
Department of Immunology, Toho University School of Medicine, Ota-ku, Tokyo, Japan
Medical Immunology, Chiba University Graduate School of Medicine, Chiba, Chiba, Japan
Molecular Immunology, Chiba University Graduate School of Medicine, Chiba, Chiba, Japan; Laboratory for Immune Regulation, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa, Japan

* Corresponding author; email: nakayama{at}faculty.chiba-u.jp.

Natural killer (NK) cells play a pivotal role in the immune reaction during the bone marrow allograft rejection. Little is known, however about the molecular mechanisms underlying the NK cell-mediated allograft recognition and rejection. In this report, we assessed the role of a recently identified NK receptor, KLRE-1, by generating knockout mice. KLRE-1-deficient mice were born at an expected frequency and showed no aberrant phenotype on growth and lymphoid development. Nevertheless, KLRE-1-deficient cells showed a severely compromised allogeneic cytotoxic activity as compared to the wild type cells. Furthermore, allogeneic bone marrow transfer culminated in colony formation in the spleen of KLRE-1-deficient mice, whereas no colony formation was observed in wild type recipient mice. These results demonstrate that KLRE-1 is a receptor mediating recognition and rejection of allogeneic target cells in the host immune system.


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