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. 2002 Feb 1;109(3):363–371. doi: 10.1172/JCI13462

Figure 2.

Figure 2

In vitro PMN function and in vivo response to thioglycollate in the absence of DPPI. (a) Bone marrow–derived PMNs from WT and DPPI–/– mice were allowed to migrate across a filter in response to 10–4 M fMLP, 2% zymosan-activated rat serum (ZAS), or 3 μg/ml rhIL-8. The number of cells that migrated was expressed as a percentage of total PMNs. Values represent the mean ± SEM of at least three animals. (b) Superoxide production by PMNs in response to PMA, expressed as nmol of O2 generated per 106 PMNs (n > 3 per genotype). The number of PMNs and macrophages recruited in response to intraperitoneal injection of thioglycollate is normal in DPPI–/– mice at 4 hours (c) 24 hours (d) and 120 hours (e).The slightly lower number of macrophages at 120 hours after thioglycollate injection in the DPPI–/– mice did not reach statistical significance (n = 4–5 mice per genotype). Mph, macrophages.