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Flightless I is a key regulator of the fibroproliferative process in hypertrophic scarring and a target for a novel antiscarring therapy
Author(s) -
Cameron A.M.,
Turner C.T.,
Adams D.H.,
Jackson J.E.,
Melville E.,
Arkell R.M.,
Anderson P.J.,
Cowin A.J.
Publication year - 2016
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.14263
Subject(s) - hypertrophic scar , fibrosis , gelsolin , medicine , myofibroblast , scars , bleomycin , regulator , disfigurement , pathology , surgery , microbiology and biotechnology , actin , chemistry , biology , chemotherapy , biochemistry , gene
Summary Background Hypertrophic scarring carries a large burden of disease, including disfigurement, pain and disability. There is currently no effective medical treatment to reduce or prevent hypertrophic scarring. Flightless I (Flii), a member of the gelsolin family of actin remodelling proteins, is an important negative regulator of wound repair. Objectives The objective of this study was to investigate the role of Flii as a potential regulator of hypertrophic scarring. Methods Using human skin samples and an animal model of bleomycin‐induced hypertrophic scarring in mice that overexpress or have reduced expression of Flii, we investigated its effect on dermal fibrosis and hypertrophic scarring. Results Flii expression was increased in human burns and hypertrophic scars. A similar increase in Flii was observed in hypertrophic scars formed in mice post‐treatment with bleomycin. However, Flii‐deficient (Flii +/− ) mice had reduced scarring in response to bleomycin evidenced by decreased dermal thickness, smaller cross‐sectional scar areas, fewer myofibroblasts and a decreased collagen I/ III ratio. In contrast, bleomycin‐treated Flii‐overexpressing mice (Flii Tg/Tg ) showed increased scar dermal thickness, larger cross‐sectional scar areas, more myofibroblasts and an increased collagen I / III ratio. Injecting developing scars with a Flii neutralizing antibody led to a significant reduction in the size of the scars and a reduction in the collagen I / III ratio. Conclusions This study identifies Flii as a profibrotic agent that contributes to excessive scar formation. Reducing its activity using neutralizing antibodies is a promising approach for reducing hypertrophic scarring.