Figure 3
Figure 3. Loss of ArhGAP15 causes increased in vitro and in vivo neutrophil migration. (A) Boyden chamber chemotaxis analysis of ArhGAP15+/+ and ArhGAP15−/− neutrophils; n = 5/genotype. (B) Representative fluorescence-activated cell sorter analysis of neutrophil CD88 and CXCR2 expression; n = 3/genotype. (C) Neutrophil recruitment to air pouches after saline (Co) or IL-8 injection; n = 6/genotype. (D-E) Peritoneal total cell recruitment and cellular subpopulation (MØ macrophages, NØ neutrophils, and LY lymphocytes) analysis after intraperitoneal administration of 1 × 107 colony-forming unit of E. coli; n = 14/genotype. #P < .05. *P < .01. **P < .001.

Loss of ArhGAP15 causes increased in vitro and in vivo neutrophil migration. (A) Boyden chamber chemotaxis analysis of ArhGAP15+/+ and ArhGAP15−/− neutrophils; n = 5/genotype. (B) Representative fluorescence-activated cell sorter analysis of neutrophil CD88 and CXCR2 expression; n = 3/genotype. (C) Neutrophil recruitment to air pouches after saline (Co) or IL-8 injection; n = 6/genotype. (D-E) Peritoneal total cell recruitment and cellular subpopulation (MØ macrophages, NØ neutrophils, and LY lymphocytes) analysis after intraperitoneal administration of 1 × 107 colony-forming unit of E. coli; n = 14/genotype. #P < .05. *P < .01. **P < .001.

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