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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.
Submitted October 10, 2003
Molecular Immunology, Chiba University Graduate School of Medicine, Chiba, Chiba, 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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| Copyright © 2004 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||