Fig. 1.
Fig. 1. The number of peritoneal mast cells is decreased in γc− and Jak3− mice. / (A) Peritoneal mast cells were recovered by lavage and counted in 8- to 12-week-old wild-type (WT), γc-deficient (γc−), and Jak3-deficient (Jak3−) mice. Peritoneal mast cells were identified morphologically on cytospin cell preparations stained with Wright-Giemsa solution. Data are means ± SD for 6 to 8 mice in each group. The mean values for γc− mice and Jak3− mice are significantly different from the mean value for WT mice, *P < .01. (B) Expression of IgE receptors on c-kit+ peritoneal cells. IgE receptors on peritoneal mast cells were quantified by first incubating the cells recovered by peritoneal lavage with mouse IgE, then labeling with anti-IgE FITC, and analyzing by FACS gating on c-kit+ cells. Shown are representative FACS profiles of IgE receptor staining and control staining (dashed lines) on c-kit+ peritoneal cells from WT, γc−, and Jak3− mice (n = 6-8 mice in each group).

The number of peritoneal mast cells is decreased in γc and Jak3 mice.

(A) Peritoneal mast cells were recovered by lavage and counted in 8- to 12-week-old wild-type (WT), γc-deficient (γc), and Jak3-deficient (Jak3) mice. Peritoneal mast cells were identified morphologically on cytospin cell preparations stained with Wright-Giemsa solution. Data are means ± SD for 6 to 8 mice in each group. The mean values for γc mice and Jak3 mice are significantly different from the mean value for WT mice, *P < .01. (B) Expression of IgE receptors on c-kit+ peritoneal cells. IgE receptors on peritoneal mast cells were quantified by first incubating the cells recovered by peritoneal lavage with mouse IgE, then labeling with anti-IgE FITC, and analyzing by FACS gating on c-kit+ cells. Shown are representative FACS profiles of IgE receptor staining and control staining (dashed lines) on c-kit+ peritoneal cells from WT, γc, and Jak3 mice (n = 6-8 mice in each group).

Close Modal

or Create an Account

Close Modal
Close Modal