Journal
FREE RADICAL BIOLOGY AND MEDICINE
Volume 44, Issue 4, Pages 682-691Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2007.10.056
Keywords
free radicals
Funding
- NIGMS NIH HHS [R01 GM077185-01A2, R01 GM077185, R01 GM069589-01A1, R01 GM069589, GM077185, GM069589] Funding Source: Medline
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We have previously reported that H2O2 is actively generated by cells at the wound site and that H2O2-driven redox signaling supports wound angiogenesis and healing. In this study, we have standardized a novel and effective electron paramagnetic resonance spectroscopy-based approach to assess the redox environment of the dermal wound site in vivo. Rac2 regulates inducible NADPH oxidase activation and other functional responses in neutrophils. Using Rac2-deficient mice we sought to investigate the significance of Rac2 in the wound-site redox environment and healing responses. Noninvasive measurements of metabolism of topically applied nitroxide N-15-perdeuterated tempone in murine excisional dermal wounds demonstrated that the wound site is rich in oxidants, the levels of which peak 2 days postwounding in the inflammatory phase. Rac2-deficient mice had threefold lower production of superoxide compared to controls with similar wounds. In these mice, a lower wound-site superoxide level was associated with compromised wound closure. Immunostaining of wound edges harvested during the inflammatory phase showed that the numbers of phagocytic cells recruited to the wound site in Rac2-deficient and control mice were similar, but the amount of lipid peroxidation was significantly lower in Rac2-deficient mice, indicating compromised NADPH oxidase activity. Taken together, the findings of this study support that the wound site is rich in oxidants. Rac2 significantly contributes to oxidant production at the wound site and supports the healing process. (c) 2007 Elsevier Inc. All rights reserved.
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