PCTR1 promotes Escherichia coli clearance during infection. A–E: Self-resolving inflammation was initiated by injecting E. coli [1 × 105 colony forming units (c.f.u.), i.p.]. Twelve hours after infection, mice were given 30 ng PCTR1/mouse or vehicle control (saline alone, i.p.). A: Quantification of peritoneal macrophages (CD11b+ F4/80+ Ly6G−). B and C: Macrophage phagocytosis of E. coli measured by flow cytometry in the peritoneum (B) and spleen (C). D: Exudate E. coli levels were assessed 24 hours after inoculation. E: PMN cell counts in the peritoneum after E. coli infection. Dotted line represents the Tmax. F: Planaria were surgically injured, kept in water with PCTR1 or vehicle control for 6 days. Dashed lines show the tissue regeneration index. Data are expressed as means ± SEM (A–F). n = 3 to 5 mice per time point (A–E); n = 12 planaria/group (F). *P ≤ 0.05, **P ≤ 0.01, and ***P ≤ 0.001, t-test, compared with E. coli alone; ††P ≤ 0.01 compared with vehicle control; ‡P ≤ 0.05, ‡‡P ≤ 0.01 at 1 nmol/L PCTR1 compared with vehicle. PCTR, protectin conjugates in tissue regeneration; PMN, Polymorphonuclear leukocyte; Ri, time interval between Tmax and T50; Tmax, point when PMN reach maximum; T50, point when PMN numbers reach 50% of maximum; (TRI)max, time to maximum tissue regeneration (Materials and Methods); TRI50, time to 50% tissue regeneration.