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. Author manuscript; available in PMC: 2014 Oct 17.
Published in final edited form as: Nature. 2014 Feb 9;508(7496):397–401. doi: 10.1038/nature13047

Figure 1. ILC lineage tracing in PLZFGFPcre reporter mice.

Figure 1

a-c, Top rows, expression of eGFP by indicated cell-types of PLZFGFPcre+/+ mice (filled grey) and WT (open); Bottom rows, YFP expression in radiation chimeras reconstituted with YFPLinSca-1+cKit+ (LSK) bone marrow cells from PLZFGFPcre+/− ROSA26-YFP mice. CLP and iILC2 from bone marrow (BM); B & T and NK from spleen; NKT from thymus (eGFP), divided in early stage 1-2 and late stage 3, and from spleen (YFP); ILC2 from lung; DX5+ and DX5 NK cells from liver; ILC1 from intestinal IEL; LTi and ILC3 from LPL. BM iILC2 and lung ILC2 were identified as LinCD25+IL-7Rα+Thy1.2+; LPL ILC2 as CD3εCD19CD25+KLRG1+; LPL NCR+ ILC3 as CD3εCD19NKp46+NK1.1; LPL CD4 LTi cells as CD3εCD19IL-7Rα+KLRG1CCR6+CD4; LPL CD4+ LTi cells as CD3εCD19CCR6+CD4+; and IEL ILC1 as CD3εCD19NKp46+NK1.1+CD160+. FACS identification of the remaining subsets is defined in the methods section. d, summary of results (mean ± s.e.m). Data representative of 3-9 individual mice analyzed in at least 2 independent experiments.