Fig. 3.
Fig. 3. Neutrophil recruitment to PAG-induced granulomas is dependent on MC-derived TNFα. / (A) Time course of PMN influx after injection of PAG inKit+/+ and KitW/KitW-vmice. Data were pooled from 10 or more mice per genotype and time point–tested in at least 7 independent experiments. (B) Impaired recruitment of PMNs to CGs inKitW/KitW-v mice is MC dependent. The dermis of KitW/KitW-v mice was reconstituted with connective tissue–type MCs from normalKit+/+ mice before PAG injection, and PMN numbers were determined 12 hours after injection of PAG. Data were pooled from 8 or more mice per genotype in at least 4 independent experiments. (C) PMN recruitment in cutaneous granuloma formation is strongly dependent on the presence of TNFα. Numbers of infiltrating PMNs were determined in PAG-injected skin of mice deficient in TNFα and in wild-type mice. Data were pooled from 5 or more mice per genotype and time point in 3 independent experiments. (D) PMN recruitment was fully restored in skin of TNF+/+ MC-reconstitutedKitW/KitW-v mice. Before PAG injection, the dermis of KitW/KitW-vmice was reconstituted with MCs from TNFα+/+ mice or TNFα-deficient mice, and numbers of PMNs were assessed 12 hours thereafter. Data were pooled from 8 or more mice per genotype in 2 independent experiments. All data in Figure 3 are shown as means ± SEMs (× 106 cells/granuloma). For all panels in Figure3, *P < .05, ***P < .005, ***P < .001.

Neutrophil recruitment to PAG-induced granulomas is dependent on MC-derived TNFα.

(A) Time course of PMN influx after injection of PAG inKit+/+ and KitW/KitW-vmice. Data were pooled from 10 or more mice per genotype and time point–tested in at least 7 independent experiments. (B) Impaired recruitment of PMNs to CGs inKitW/KitW-v mice is MC dependent. The dermis of KitW/KitW-v mice was reconstituted with connective tissue–type MCs from normalKit+/+ mice before PAG injection, and PMN numbers were determined 12 hours after injection of PAG. Data were pooled from 8 or more mice per genotype in at least 4 independent experiments. (C) PMN recruitment in cutaneous granuloma formation is strongly dependent on the presence of TNFα. Numbers of infiltrating PMNs were determined in PAG-injected skin of mice deficient in TNFα and in wild-type mice. Data were pooled from 5 or more mice per genotype and time point in 3 independent experiments. (D) PMN recruitment was fully restored in skin of TNF+/+ MC-reconstitutedKitW/KitW-v mice. Before PAG injection, the dermis of KitW/KitW-vmice was reconstituted with MCs from TNFα+/+ mice or TNFα-deficient mice, and numbers of PMNs were assessed 12 hours thereafter. Data were pooled from 8 or more mice per genotype in 2 independent experiments. All data in Figure 3 are shown as means ± SEMs (× 106 cells/granuloma). For all panels in Figure3, *P < .05, ***P < .005, ***P < .001.

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