(A) Histograms of Ly49H expression on splenic
Ly49H+ NK cells (gating strategy in Figure S1A) from uninfected (UI)
and MCMV-infected WT mice at day 7 PI (D7). Data are representative of at least
five independent experiments with 5–10 mice per experiment.
(B-C) Experimental schematic (B). Ly49H+ NK
cells were transferred into
Klra8−/−
mice, and their phenotype analyzed following MCMV infection of the recipients.
(C) Histograms of Ly49H expression on Ly49H+ NK cells from blood of
UI WT mice (shaded gray) versus at day 7 PI (top left) and day 29 PI (bottom
left) (black lines). Quantification of Ly49H median fluorescence intensity (MFI)
on Ly49H+ NK cells at indicated days PI relative to UI WT mice bled
on the same day (right). Data are representative of three independent
experiments with 10–25 mice per experiment.
(D) As in (C), histograms (left) and MFI (right) of NK1.1
on Ly49H+ NK cells from blood of UI WT mice and at day 28 PI. Data
are representative of at least three independent experiments with 3–9
mice per experiment.
(E) WT mice were infected with MCMV,
MCMV-Δm157, Listeria monocytogenes
(L.m.) or UI. Data is represented as Ly49H MFI on
Ly49H+ NK cells from blood at day 7 PI for indicated infections
relative to UI. Data are representative of two independent experiments with
2–5 mice per group.
(F) As in (B), except splenocytes from WT and indicated
knock-out (KO) mice were co-transferred. Data is represented as Ly49H MFI on KO
Ly49H+ NK cells relative to WT from blood at day 7 PI. Data are
representative of two to four independent experiments with 2–5 mice per
group. Groups with a ratio < 1 were compared against 1 using a one sample
t test.
Groups were compared using an unpaired, two-tailed Student’s t
test (D) or against 1 using a one sample t test (E). In (C), each timepoint was
compared against 1 using a one sample t test, and against each other using a
paired two-tailed t test. Data are presented as the mean ± SEM. *p
< 0.05; ****p < 0.0001. See also Figure S1.