Skip to main content
. 2019 Jan 8;9:3108. doi: 10.3389/fimmu.2018.03108

Figure 1.

Figure 1

Loss of JAK1 in NKp46+ cells leads to an almost complete absence of peripheral NK cells. (A) Frequency (left panel) and total numbers (right panel) of Lin(CD3CD19Ly-6GTer119) CD122+ NK cells in the bone marrow were assessed by flow cytometry. (B) Bone marrow LinCD122+ cells were further divided into NK precursors (NKPs: NKp46NK1.1), immature NK cells (iNKs: NKp46NK1.1+), and mature NK cells (mNKs: NKp46+NK1.1+). (C) Frequency of CD3NKp46+ NK cells in the spleen was assessed by flow cytometry and representative plots are shown. (D,E) Frequency (left panel) and total numbers (right panel) of CD3NKp46+ NK cells in the (D) spleen and (E) blood were assessed by flow cytometry. (F) Frequency of conventional NK cells (CD3NK1.1+NKp46+CD49b+, left panel) and ILC1 cells (CD3NK1.1+NKp46+CD49a+, right panel) was analyzed in the liver of Jak1WT, Jak1fl/+Ncr1Cre, and Jak1fl/flNcr1Cre mice by flow cytometry. (A,B,D–F) Bar graphs represent mean ± SEM of 1–2 independent experiments; n = 3–11. *p < 0.05, **p < 0.01, ***p < 0.001.