Figure 5
Figure 5. Neutrophil recruitment in a model of LPS-induced lung inflammation and thioglycollate-induced peritonitis is partially dependent on Gαi2 in neutrophils. (A) Neutrophil recruitment into the alveolar compartments of the lung with or without LPS inhalation (24 hours) was determined by flow cytometry. Gnai2−/− mice, Gnai2+/+ mice, and Gnai2−/− → Gnai2+/+ chimeric mice showed different recruitment patterns of neutrophils in the alveolar compartment (n = 4). Data are means plus or minus SEM. (B) Peritoneal neutrophil influx 4 hours after injection of 4% thioglycollate into Gnai2−/− mice (4 mice), Gnai2−/− mice (3 mice), Gnai2−/− → Gnai2+/+ chimeric mice (5 mice), and Gnai2+/+ → Gnai2+/+ mice (5 mice). Total number of neutrophils (× 106) in the peritoneal cavity counted using Kimura-stained samples. Horizontal bars are means of 5 replicates. *P < .05 versus other groups; #P < .05.

Neutrophil recruitment in a model of LPS-induced lung inflammation and thioglycollate-induced peritonitis is partially dependent on Gαi2 in neutrophils. (A) Neutrophil recruitment into the alveolar compartments of the lung with or without LPS inhalation (24 hours) was determined by flow cytometry. Gnai2−/− mice, Gnai2+/+ mice, and Gnai2−/−Gnai2+/+ chimeric mice showed different recruitment patterns of neutrophils in the alveolar compartment (n = 4). Data are means plus or minus SEM. (B) Peritoneal neutrophil influx 4 hours after injection of 4% thioglycollate into Gnai2−/− mice (4 mice), Gnai2−/− mice (3 mice), Gnai2−/−Gnai2+/+ chimeric mice (5 mice), and Gnai2+/+Gnai2+/+ mice (5 mice). Total number of neutrophils (× 106) in the peritoneal cavity counted using Kimura-stained samples. Horizontal bars are means of 5 replicates. *P < .05 versus other groups; #P < .05.

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