Literature DB >> 19519830

Attenuation of Flightless I, an actin-remodelling protein, improves burn injury repair via modulation of transforming growth factor (TGF)-beta1 and TGF-beta3.

D H Adams1, N Ruzehaji, X L Strudwick, J E Greenwood, H D Campbell, R Arkell, A J Cowin.   

Abstract

BACKGROUND: The pathophysiological mechanisms involved in burn injury repair are still not fully understood but include processes involving cellular proliferation, migration and adhesion. The actin cytoskeleton is intricately involved in these key wound repair processes. Flightless I (Flii), an actin-remodelling protein and transcriptional regulator, is an important regulator of wound healing.
OBJECTIVES: To investigate the function of Flii gene expression in burn injury repair.
METHODS: Partial-thickness scald wounds were created on Flii heterozygous (Flii(+/-)), wild-type (WT) and Flii transgenic (Flii(Tg/+)) mice. Burns were assessed using histology and immunohistochemistry, real-time quantitative polymerase chain reaction and biochemical analysis.
RESULTS: Flii expression, while upregulated in burn injuries, was significantly lower in the wounds of Flii(+/-) vs. WT vs. Flii(Tg/+) mice and healing was improved in Flii(+/-) mice with their burns healing faster than WT and Flii(Tg/+). Pro-scarring transforming growth factor (TGF)-beta1 protein and gene expression were reduced in Flii(+/-) burns while antiscarring TGF-beta3 was significantly elevated. Anti-alpha-smooth muscle actin (alpha-SMA) was decreased in Flii(+/-) burns suggesting a decrease in contractile myofibroblasts in the developing scars. Although Flii is primarily a nuclear and cytoplasmic protein it is also released by wounded cells. Intradermal injection of Flii-neutralizing antibodies (FliAbs) to WT burn wounds significantly improved their healing, indicating a potential novel approach for treating burns. Decreased TGF-beta1 and elevated TGF-beta3 expression were observed in FliAb-treated burns, which may contribute to their observed improvement in healing.
CONCLUSIONS: Strategies aimed at reducing Flii expression, for example using neutralizing antibodies, may lead to improved burn outcomes.

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Year:  2009        PMID: 19519830     DOI: 10.1111/j.1365-2133.2009.09296.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  19 in total

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Review 2.  Animal models in burn research.

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Authors:  Xanthe L Strudwick; Damian H Adams; Natasha T Pyne; Michael S Samuel; Rachael Z Murray; Allison J Cowin
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5.  Attenuation of flightless I improves wound healing and enhances angiogenesis in a murine model of type 1 diabetes.

Authors:  Nadira Ruzehaji; Zlatko Kopecki; Elizabeth Melville; Sarah L Appleby; Claudine S Bonder; Ruth M Arkell; Robert Fitridge; Allison J Cowin
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Journal:  Burns       Date:  2021-04-20       Impact factor: 2.744

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Authors:  Yiu-Hei Ching; Thomas L Sutton; Yvonne N Pierpont; Martin C Robson; Wyatt G Payne
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9.  Lysosomal secretion of Flightless I upon injury has the potential to alter inflammation.

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10.  The influence of Flightless I on Toll-like-receptor-mediated inflammation in a murine model of diabetic wound healing.

Authors:  Nadira Ruzehaji; Stuart J Mills; Elizabeth Melville; Ruth Arkell; Robert Fitridge; Allison J Cowin
Journal:  Biomed Res Int       Date:  2013-02-18       Impact factor: 3.411

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