NKp46 plays a cell-intrinsic role in regulating ILC1 development.

Abstract

<p>(A) Scheme of BM transplantation using BM cells of CD45.2 <i>Ncr1</i><sup>gfp/gfp</sup> mice or <i>Ncr1</i><sup>+/+</sup> littermate controls as donor cells to inject into CD45.1 recipients via tail vein. Development of ILC subsets was analyzed 2 weeks after transplantation. (B) Percentages of CD45.2<sup>+</sup> NK cells or CD45.2<sup>+</sup> ILC1s were analyzed by flow cytometric analysis in the liver of CD45.1 recipients, which were engrafted with BM cells of <i>Ncr1</i><sup>gfp/gfp</sup> mice (<i>n</i> = 5) or <i>Ncr1</i><sup>+/+</sup> littermates (<i>n</i> = 4). (C) Percentages of CD45.2<sup>+</sup> NK cells or CD45.2<sup>+</sup> ILC1s were analyzed in the spleen or BM of CD45.1 recipient mice, which were engrafted with BM cells of <i>Ncr1</i><sup>gfp/gfp</sup> mice (<i>n</i> = 5) or their <i>Ncr1</i><sup>+/+</sup> littermates (<i>n</i> = 4). (D and E) Data shown are representative dot plots of flow cytometric analysis (left panel) and summary data (right panel) of CD45.2<sup>+</sup>ILC2 (D) or CD45.2<sup>+</sup> ILC3 (E) in SI in CD45.1 recipients, which were engrafted with BM cells of <i>Ncr1</i><sup>gfp/gfp</sup> mice (<i>n</i> = 4) or their <i>Ncr1</i><sup>+/+</sup> littermates (<i>n</i> = 4). Error bars, standard deviations; ***, <i>p</i> < 0.001; **, <i>p</i> < 0.01; *, <i>p</i> < 0.05. The numerical data for panels B, C, D and E can be found in <a href="http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.2004867#pbio.2004867.s007" target="_blank">S1 Data</a>. Lin<sup>─</sup>, CD3<sup>─</sup>CD19<sup>─</sup>; BM, bone marrow; ILC, innate lymphoid cells; <i>Ncr1</i>, natural cytotoxicity receptor 1; NK, natural killer; RORγt, retinoic acid receptor (RAR) related orphan receptor gamma t; SI, small intestine.</p

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