Rac inhibition reverses the phenotype of fibrotic fibroblasts

Shi-Wen, X., Liu, S., Eastwood, M., Sonnylal, S., Denton, C.P., Abraham, D.J. and Leask, A. 2009. Rac inhibition reverses the phenotype of fibrotic fibroblasts. PLoS ONE. 4 (10) e7438. https://doi.org/10.1371/journal.pone.0007438

TitleRac inhibition reverses the phenotype of fibrotic fibroblasts
TypeJournal article
AuthorsShi-Wen, X., Liu, S., Eastwood, M., Sonnylal, S., Denton, C.P., Abraham, D.J. and Leask, A.
Abstract

Background

Fibrosis, the excessive deposition of scar tissue by fibroblasts, is one of the largest groups of diseases for which there is no therapy. Fibroblasts from lesional areas of scleroderma patients possess elevated abilities to contract matrix and produce α−smooth muscle actin (α-SMA), type I collagen and CCN2 (connective tissue growth factor, CTGF). The basis for this phenomenon is poorly understood, and is a necessary prerequisite for developing novel, rational anti-fibrotic strategies.

Methods and Findings

Compared to healthy skin fibroblasts, dermal fibroblasts cultured from lesional areas of scleroderma (SSc) patients possess elevated Rac activity. NSC23766, a Rac inhibitor, suppressed the persistent fibrotic phenotype of lesional SSc fibroblasts. NSC23766 caused a decrease in migration on and contraction of matrix, and α−SMA, type I collagen and CCN2 mRNA and protein expression. SSc fibroblasts possessed elevated Akt phosphorylation, which was also blocked by NSC23766. Overexpression of rac1 in normal fibroblasts induced matrix contraction and α−SMA, type I collagen and CCN2 mRNA and protein expression. Rac1 activity was blocked by PI3kinase/Akt inhibition. Basal fibroblast activity was not affected by NSC23766.

Conclusion

Rac inhibition may be considered as a novel treatment for the fibrosis observed in SSc.

Article numbere7438
JournalPLoS ONE
Journal citation4 (10)
ISSN1932-6203
Year2009
PublisherPublic Library of Science
Digital Object Identifier (DOI)https://doi.org/10.1371/journal.pone.0007438
Publication dates
Published13 Oct 2009

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