Fig. 3: Concomitant with diminished Th2 and ILC2 responses, MIF deficiency leads to impaired eosinophil recruitment and alternative macrophage polarisation in the peritoneal cavity. | Mucosal Immunology

Fig. 3: Concomitant with diminished Th2 and ILC2 responses, MIF deficiency leads to impaired eosinophil recruitment and alternative macrophage polarisation in the peritoneal cavity.

From: The IL-25-dependent tuft cell circuit driven by intestinal helminths requires macrophage migration inhibitory factor (MIF)

Fig. 3

Mice of both genotypes were infected with 400 L3 N. brasiliensis larvae by s.c. injection, and samples recovered at day 6 for cellular and ELISA analysis, using the gating strategy described in Fig. S3B. a Total peritoneal lavage cells recovered from infected mice (n = 8) and naive controls (n = 7), combined data from two independent experiments. b Siglec-F+ eosinophils recovered from infected mice (n = 5) and naive controls (n = 3) enumerated by flow cytometry. Alternatively activated CD11b+F4/80+ macrophages evaluated by expression of RELMα (c), and Chil3/Ym1 (d) in samples from infected mice (n = 5) and naive controls (n = 3), enumerated by flow cytometry. e, f Concentrations of RELMα (j) and Chil3/Ym1 (k) in the peritoneal lavage fluid measured by ELISA, in samples from infected mice (n = 3–4) and naive controls (n = 3). Data are presented as arithmetic means and standard errors, and bf are representative of at least two individually performed experiments; data were statistically analysed by unpaired t tests. *P < 0.05, **P < 0.01.

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