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Fig. 1 | Journal of Biomedical Science

Fig. 1

From: IL-33 receptor (ST2) deficiency downregulates myeloid precursors, inflammatory NK and dendritic cells in early phase of sepsis

Fig. 1

Deletion of ST2 accelerates CLP induced polymicrobial sepsis and affects granulocytes influx into peritoneal cavity. Clinical score and survival rate of septic ST2−/− and WT mice was monitored every 6 h. a ST2−/− mice exhibit significantly increased clinical score during first 18 h following CLP. b Survival rate of septic ST2−/− and WT mice was analyzed by Fisher’s exact test for each time point. ST2−/− mice had significantly decreased survival rate at 36, 42 and 48 h following CLP (n = 22 mice per group). c Significantly decreased number of peritoneal cells in septic ST2−/− in comparison with WT mice 12 h following CLP. The number of peritoneal neutrophils (CD11b+Ly6G+) (d), eosinophils (CD11b+Siglec-F+) (e), mast cells (CD117+FcεRI+) (f) and macrophages (g) 12 h following CLP. Data are presented as mean ± SE, n = 4–7 mice per group. *p < 0.05, **p < 0.01

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