Figure 6.
Figure 6. Mac-1 is critical to macrophage migration in vivo to the lymphatics. The GFP+ WT peritoneal macrophages were injected intraperitoneally into the TG-preconditioned WT mice with and without NIF, followed with intraperitoneal injections of PBS or LPS. (A) The number of GFP+ cells within the peritoneum (left) or the draining lymph nodes (right) was determined 4 hours later. The data represent the mean ± SD of 2 independent experiments. (B-D) PKH26-labeled Mac-1-/- peritoneal macrophages were injected intraperitoneally into the TG-preconditioned Mac-1-/- mice, followed by intraperitoneal injections of PBS or LPS. The number of fluorescent Mac-1-/- macrophages within the peritoneum (B), adherent on the peritoneal membrane (C), or within the blood circulation (D) was determined 4 hours later. The data represent the mean ± SD of 2 independent experiments. **P < .01; *P < .05.

Mac-1 is critical to macrophage migration in vivo to the lymphatics. The GFP+ WT peritoneal macrophages were injected intraperitoneally into the TG-preconditioned WT mice with and without NIF, followed with intraperitoneal injections of PBS or LPS. (A) The number of GFP+ cells within the peritoneum (left) or the draining lymph nodes (right) was determined 4 hours later. The data represent the mean ± SD of 2 independent experiments. (B-D) PKH26-labeled Mac-1-/- peritoneal macrophages were injected intraperitoneally into the TG-preconditioned Mac-1-/- mice, followed by intraperitoneal injections of PBS or LPS. The number of fluorescent Mac-1-/- macrophages within the peritoneum (B), adherent on the peritoneal membrane (C), or within the blood circulation (D) was determined 4 hours later. The data represent the mean ± SD of 2 independent experiments. **P < .01; *P < .05.

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