Figure 7
Figure 7. Leukocyte recruitment in cremasteric postcapillary venules of TNFα-treated chimeric mice. (A) The leukocyte rolling flux, (B) rolling velocity, (C) adhesion, and (D) emigration are shown. WT and PI3Kγ-/- mice were reconstituted with PI3Kγ-/- and WT bone marrow, indicated as PI3Kγ-/-→WT and WT→ PI3Kγ-/-, respectively. Leukocyte recruitment was induced by intrascrotal injection of TNFα (0.5 μg in 200 μL saline) and the recruitment parameters determined in cremasteric venules from these chimeric mice (n = 5 in each group) at 4 hours, 4.5 hours, and 5 hours. **P < .01 as compared with groups of opposite chimeric mice. Error bars represent means plus or minus SEM.

Leukocyte recruitment in cremasteric postcapillary venules of TNFα-treated chimeric mice. (A) The leukocyte rolling flux, (B) rolling velocity, (C) adhesion, and (D) emigration are shown. WT and PI3Kγ-/- mice were reconstituted with PI3Kγ-/- and WT bone marrow, indicated as PI3Kγ-/-→WT and WT→ PI3Kγ-/-, respectively. Leukocyte recruitment was induced by intrascrotal injection of TNFα (0.5 μg in 200 μL saline) and the recruitment parameters determined in cremasteric venules from these chimeric mice (n = 5 in each group) at 4 hours, 4.5 hours, and 5 hours. **P < .01 as compared with groups of opposite chimeric mice. Error bars represent means plus or minus SEM.

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