Figure 4
Figure 4. Adoptive transfer of PMNs and recruitment to S aureus–infected wounds. (A) FACS sorting of mature EGFP-PMNs (c-kit−EGFPhighGr-1highCD11bhigh cells) and cytospin image. To avoid any inclusion of cells with proliferative capacity, c-kit+-progenitor cells were gated out. The FACS-sorted cells were intravenously transferred (5 × 106 cells in 0.1 mL of sterile saline) to C57BL/6 mice whose wounds were treated with either sterile saline or S aureus (1 × 107 CFUs), and the kinetics of EGFP-PMNs within the wound were determined (B). (C) The half-life of wound EGFP-PMNs was quantified from EGFP-PMN kinetic data using the equations described in the supplemental Methods. Data are derived from 4 mice in each group and are expressed as means ± SEM. *P < .01 vs saline control group.

Adoptive transfer of PMNs and recruitment to S aureus–infected wounds. (A) FACS sorting of mature EGFP-PMNs (c-kitEGFPhighGr-1highCD11bhigh cells) and cytospin image. To avoid any inclusion of cells with proliferative capacity, c-kit+-progenitor cells were gated out. The FACS-sorted cells were intravenously transferred (5 × 106 cells in 0.1 mL of sterile saline) to C57BL/6 mice whose wounds were treated with either sterile saline or S aureus (1 × 107 CFUs), and the kinetics of EGFP-PMNs within the wound were determined (B). (C) The half-life of wound EGFP-PMNs was quantified from EGFP-PMN kinetic data using the equations described in the supplemental Methods. Data are derived from 4 mice in each group and are expressed as means ± SEM. *P < .01 vs saline control group.

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