Figure 6
Figure 6. Flip deletion results in increased neutrophils and decreased macrophages in the peritoneum. Resident (A-B) or thioglycollate elicited (E-F) cells from peritoneal cavities were analyzed by flow cytometry, gaiting on CD11b+ cells. The macrophages (MΦ) were identified as F4/80+, Gr1−, whereas granulocytes (Gran) were identified as F4/80−, Gr1+. (B) The total number of cells, resident macrophages and granulocytes from controls (n = 20) and Flipf/d, LysMc/+ mice (n = 26) are summarized. (C) There was an inverse relationship between the percentage of peritoneal macrophages and granulocytes in the wild-type and Flipf/d, LysMc/+ mice. (D) PCR genotyping of granulocytes and macrophages isolated from peritoneal cavities were performed using the 3 PCR primers indicated in Figure 1. (F) The total number of thioglycollate elicited macrophages and granulocytes at 72 hours (n = 7 for each group) are summarized. *P < .05, **P < .01, and ***P < .001 between groups.

Flip deletion results in increased neutrophils and decreased macrophages in the peritoneum. Resident (A-B) or thioglycollate elicited (E-F) cells from peritoneal cavities were analyzed by flow cytometry, gaiting on CD11b+ cells. The macrophages (MΦ) were identified as F4/80+, Gr1, whereas granulocytes (Gran) were identified as F4/80, Gr1+. (B) The total number of cells, resident macrophages and granulocytes from controls (n = 20) and Flipf/d, LysMc/+ mice (n = 26) are summarized. (C) There was an inverse relationship between the percentage of peritoneal macrophages and granulocytes in the wild-type and Flipf/d, LysMc/+ mice. (D) PCR genotyping of granulocytes and macrophages isolated from peritoneal cavities were performed using the 3 PCR primers indicated in Figure 1. (F) The total number of thioglycollate elicited macrophages and granulocytes at 72 hours (n = 7 for each group) are summarized. *P < .05, **P < .01, and ***P < .001 between groups.

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