Fig. 3.
Fig. 3. The circulating life spans of CD18-deficient neutrophils is not increased compared with WT. / C57BL/6-CD45.1 host animals were injected intravenously with mixtures of blood collected from WT and CD18-deficient animals. (A) The numbers of blood neutrophils (Gr-1bright), which were of donor origin (CD45.2+), were determined by counting and flow cytometry at the indicated time points after injection. (B, C) The percentage of donor neutrophils (CD45.2+, Gr-1bright) that were CD18-deficient (CD11a−) was determined by flow cytometry at the indicated time points. The data point at time 0 refers to the percentage of CD18-deficient neutrophils in the original mixture before injection into the host animal. * indicates significant (P < .05) decrease in the percentage of CD18-deficient neutrophils compared with the earlier time points. Each point represents the mean ± SEM for 4 host mice.

The circulating life spans of CD18-deficient neutrophils is not increased compared with WT.

C57BL/6-CD45.1 host animals were injected intravenously with mixtures of blood collected from WT and CD18-deficient animals. (A) The numbers of blood neutrophils (Gr-1bright), which were of donor origin (CD45.2+), were determined by counting and flow cytometry at the indicated time points after injection. (B, C) The percentage of donor neutrophils (CD45.2+, Gr-1bright) that were CD18-deficient (CD11a) was determined by flow cytometry at the indicated time points. The data point at time 0 refers to the percentage of CD18-deficient neutrophils in the original mixture before injection into the host animal. * indicates significant (P < .05) decrease in the percentage of CD18-deficient neutrophils compared with the earlier time points. Each point represents the mean ± SEM for 4 host mice.

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