Fig. 4.
Fig. 4. Neutrophil influx into the peritoneal cavity during thioglycolate-induced peritonitis. / Thioglycolate was injected into the peritoneal cavity of 4 to 8 wild-type mice (diamonds) or triple-null mice (squares). Values represent the mean ± SD number of neutrophils recovered from peritoneal lavage at the indicated times. The differences between the triple-selectin–null mice and the wild-type mice were significant (P < .001) at all times studied. Solid circles represent the number of neutrophils collected after intravenous administration of the α4-integrin–blocking mAb PS/2 to triple-null mice 1 hour before and 6 hours after thioglycolate injection. Although we hypothesized that this blocking antibody might reduce neutrophil emigration into the peritoneal cavity, we observed no effect in this model.

Neutrophil influx into the peritoneal cavity during thioglycolate-induced peritonitis.

Thioglycolate was injected into the peritoneal cavity of 4 to 8 wild-type mice (diamonds) or triple-null mice (squares). Values represent the mean ± SD number of neutrophils recovered from peritoneal lavage at the indicated times. The differences between the triple-selectin–null mice and the wild-type mice were significant (P < .001) at all times studied. Solid circles represent the number of neutrophils collected after intravenous administration of the α4-integrin–blocking mAb PS/2 to triple-null mice 1 hour before and 6 hours after thioglycolate injection. Although we hypothesized that this blocking antibody might reduce neutrophil emigration into the peritoneal cavity, we observed no effect in this model.

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