Journal
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
Volume 36, Issue 4, Pages 985-991Publisher
SPANDIDOS PUBL LTD
DOI: 10.3892/ijmm.2015.2299
Keywords
shikonin; transforming growth factor-beta 1; hypetrophic scar; fibroblasts; collagen
Categories
Funding
- Australian Government's Cooperative Research Centres Program
- Queensland University of Technology (QUT) Tissue Repair and Regeneration Program
- Wound Management Innovation Cooperative Research Centre
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Hypertrophic scarring/hypertrophic scars (HS) is a highly prevalent condition following burns and trauma wounds. Numerous studies have demonstrated that transforming growth factor-beta 1 (TGF-beta 1) plays an essential role in the wound healing process by regulating cell differentiation, collagen production and extracellular matrix degradation. The increased expression of TGF-beta 1 is believed to result in the formation of HS. Shikonin (SHI), an active component extracted from the Chinese herb, Radix Arnebiae, has previously been found to downregulate the expression of TGF-beta 1 in keratinocyte/fibroblast co-culture conditioned medium. In view of this, in this study, we aimed to further investigate the effects of SHI on TGF-beta 1-stimulated hypertrophic scar-derived human skin fibroblasts (HSFs) and examined the underlying mechanisms. Cell viability and proliferation were measured using alamarBlue and CyQUANT assays. The total amount of collagen and cell contraction were examined using Sirius red staining and the cell contraction assay kit. Gene expression and signalling pathway activation were detected using reverse transcription-quantitative polymerase chain reaction and western blot analysis. Our results revealed that SHI reduced TGF-beta 1-induced collagen production through the ERK/Smad signalling pathway and attenuated TGF-beta 1-induced cell contraction by downregulating a-smooth muscle actin (alpha SMA) expression in the HSFs. The data from this study provide evidence supporting the potential use of SHI as a novel treatment for HS.
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