Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/79547
Title: In vitro analyses of the anti-fibrotic effect of SPARC silencing in human Tenon’s fibroblasts : comparisons with mitomycin C
Authors: Seet, Li-Fong
Su, Roseline
Toh, Li Zhen
Wong, Tina T.
Issue Date: 2011
Source: Seet, L.-F., Su, R., Toh, L. Z., & Wong, T. T. (2012). In vitro analyses of the anti-fibrotic effect of SPARC silencing in human Tenon’s fibroblasts: comparisons with mitomycin C. Journal of Cellular and Molecular Medicine, 16(6), 1245-1259.
Series/Report no.: Journal of cellular and molecular medicine
Abstract: Failure of glaucoma filtration surgery (GFS) is commonly attributed to scarring at the surgical site. The human Tenon’s fibroblasts (HTFs) are considered the major cell type contributing to the fibrotic response. We previously showed that SPARC (secreted protein, acidic, rich in cysteine) knockout mice had improved surgical success in a murine model of GFS. To understand the mechanisms of SPARC deficiency in delaying subconjunctival fibrosis, we used the gene silencing approach to reduce SPARC expression in HTFs and examined parameters important for wound repair and fibrosis. Mitomycin C-treated HTFs were used for comparison. We demonstrate that SPARC-silenced HTFs showed normal proliferation and negligible cellular necrosis but were impaired in motility and collagen gel contraction. The expression of pro-fibrotic genes including collagen I, MMP-2, MMP-9, MMP-14, IL-8, MCP-1 and TGF-β2 were also reduced. Importantly, TGF-β2 failed to induce significant collagen I and fibronectin expressions in the SPARC-silenced HTFs. Together, these data demonstrate that SPARC knockdown in HTFs modulates fibroblast functions important for wound fibrosis and is therefore a promising strategy in the development of anti-scarring therapeutics.
URI: https://hdl.handle.net/10356/79547
http://hdl.handle.net/10220/17837
ISSN: 1582-1838
DOI: 10.1111/j.1582-4934.2011.01400.x
Schools: School of Materials Science & Engineering 
Rights: © 2011 The Authors. This paper was published in Journal of Cellular and Molecular Medicine and is made available as an electronic reprint (preprint) with permission of the authors. The paper can be found at the following official DOI: [http://dx.doi.org/10.1111/j.1582-4934.2011.01400.x]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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