A defective Il15 allele underlies the deficiency in natural killer cell activity in nonobese diabetic mice |
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Authors: | Hirotsugu Suwanai Martha Angela Wilcox Diane Mathis Christophe Benoist |
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Affiliation: | aSection on Immunology and Immunogenetics, Joslin Diabetes Center, Boston, MA 02215; and;bDepartment of Pathology, Harvard Medical School, The Broad Institute and The Harvard Stem Cell Institute, Boston, MA 02115 |
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Abstract: | The nonobese diabetic (NOD) mouse strain has a genetic deficiency in natural killer (NK) cells. This defect underlies this strain''s utility in several experimental settings; in particular, it promotes engraftment of human tissue in NOD hosts during the generation of “humanized” mouse models. We have mapped the major NK-cell defect in the NOD vs. C57BL/6 (B6) strain to an inadequately expressed Il15 allele. Treatment of NOD mice with a reagent that specifically enhances interleukin (IL)-15 bioavailability normalized NK-cell numbers and activity in the absence of nonspecific stimulation. These findings raise the possibility of exploiting reagents that impact the IL-15 receptor pathway to facilitate construction of humanized mouse models on non-NOD genetic backgrounds. |
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Keywords: | type 1 diabetes gene mapping cytotoxicity genetic variation |
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