Figure 6
Figure 6. H2O2 can mediate the antiproliferative effect of IL4I1. CD45RO+ and CD45RA+ T cells were incubated through a 0.4-μm transwell for 3 hours with mock beads, hIL4I1 beads, or E481A-hIL4I1 beads (A) or in the presence of increasing concentrations of H2O2 (B) or phenylpyruvate (C) and analyzed for 3H-thymidine incorporation. Results are expressed as the average cpm of quadruplicates ± SD. (B-C) CD45RO+ (○) and CD45RA+ (●). A representative experiment (of 4) is shown. *P < .05. (D) Proliferation was assessed on T cells incubated with 50 μM H2O2 or with 10 μL mock beads or hIL4I1 beads through a 0.4-μm transwell for 3 hours with or without preincubation with 1000 U/mL catalase. Results are expressed as the average cpm of sextuplicate samples ± SD. A representative experiment is shown. *P = .04; **P < .005.

H2O2 can mediate the antiproliferative effect of IL4I1. CD45RO+ and CD45RA+ T cells were incubated through a 0.4-μm transwell for 3 hours with mock beads, hIL4I1 beads, or E481A-hIL4I1 beads (A) or in the presence of increasing concentrations of H2O2 (B) or phenylpyruvate (C) and analyzed for 3H-thymidine incorporation. Results are expressed as the average cpm of quadruplicates ± SD. (B-C) CD45RO+ (○) and CD45RA+ (●). A representative experiment (of 4) is shown. *P < .05. (D) Proliferation was assessed on T cells incubated with 50 μM H2O2 or with 10 μL mock beads or hIL4I1 beads through a 0.4-μm transwell for 3 hours with or without preincubation with 1000 U/mL catalase. Results are expressed as the average cpm of sextuplicate samples ± SD. A representative experiment is shown. *P = .04; **P < .005.

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