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. 2022 Nov 3;13:6603. doi: 10.1038/s41467-022-34080-4

Fig. 5. RIPK1 Y383F mice develop systemic inflammation and emergency hematopoiesis.

Fig. 5

a Representative images of spleen tissue and statistical results of spleen weight from Ripk1+/+ (n = 5) and Ripk1Y383F/Y383F (n = 5) female mice at age of 6 weeks. b Flow cytometry and statistical analysis of neutrophils (CD11b+Ly6G+) and monocytes (CD11b+Ly6C+) in the spleen of Ripk1+/+ (n = 5) and Ripk1Y383F/Y383F (n = 5) mice at 8 weeks of age. c Immunohistochemical staining of CD11b, Ly6G, CD45 or F4/80 in liver sections of Ripk1+/+ and Ripk1Y383F/Y383F littermate mice at age of 8 weeks (Scale bar, 100 μm). Flow cytometry and statistical analysis in bone marrow for the indicated hematopoietic populations: LKs, LSKs, HSCs (d) and GMPs, MEPs, CMPs (e) from Ripk1+/+ (n = 5) and Ripk1Y383F/Y383F (n = 5) mice at age of 8 weeks. f Images of spleen tissue and statistical analysis of spleen weight in Ripk1+/+ » WT (n = 5) and Ripk1Y383F/Y383F » WT (n = 5) transplant mice at age of 8 weeks. g Flow cytometry and statistical analysis of neutrophils in the spleen from Ripk1+/+ » WT (n = 5) and Ripk1Y383F/Y383F » WT (n = 5) transplant mice at age of 8 weeks. Data are represented as mean ± SEM. Statistical significance was determined using a two-tailed unpaired t test. n.s. p > 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001. Source data are provided with this paper.