1. Effects of ranibizumab on the extracellular matrix production by human Tenon's fibroblast
- Author
-
Sushil Kumar R Vasudevan, Siti Munirah Md Noh, Narimah Abdul Hamid Hasani, Hapizah Md Nawawi, Jonathan G Crowston, Zakaria Bannur, Siti Hamimah Sheikh Abdul Kadir, and Gabriele Ruth Anisah Froemming
- Subjects
Vascular Endothelial Growth Factor A ,genetic structures ,Cell Survival ,Tenon Capsule ,Cell Culture Techniques ,Angiogenesis Inhibitors ,Enzyme-Linked Immunosorbent Assay ,Trabeculectomy ,Antibodies, Monoclonal, Humanized ,Real-Time Polymerase Chain Reaction ,Collagen Type I ,Andrology ,Cellular and Molecular Neuroscience ,Ranibizumab ,medicine ,Humans ,Vimentin ,MTT assay ,RNA, Messenger ,Viability assay ,Fluorescent Antibody Technique, Indirect ,Fibroblast ,Cell Proliferation ,biology ,Chemistry ,Cell growth ,Fibroblasts ,Sensory Systems ,Fibronectins ,Collagen Type I, alpha 1 Chain ,Fibronectin ,Ophthalmology ,Vascular endothelial growth factor A ,medicine.anatomical_structure ,Gene Expression Regulation ,Cell culture ,Immunology ,biology.protein ,Glaucoma, Open-Angle ,medicine.drug - Abstract
Anti-Vascular Endothelial Growth Factors (Anti-VEGF) agents have received recent interest as potential anti-fibrotic agents for their concurrent use with trabeculectomy. Preliminary cohort studies have revealed improved bleb morphology following trabeculectomy augmented with ranibizumab. The effects of this humanized monoclonal antibody on human Tenon's fibroblast (HTF), the key player of post trabeculectomy scar formation, are not fully understood. This study was conducted to understand the effects of ranibizumab on extracellular matrix production by HTF. The effect of ranibizumab on HTF proliferation and cell viability was determined using MTT assay (3-(4,5-dimethylthiazone-2-yl)-2,5-diphenyl tetrazolium). Ranibizumab at concentrations ranging from 0.01 to 0.5 mg/mL were administered for 24, 48 and 72 h in serum and serum free conditions. Supernatants and cell lysates from samples were assessed for collagen type 1 alpha 1 and fibronectin mRNA and protein level using quantitative real time polymerase chain reaction (qRT-PCR) and enzyme-linked immunosorbent assay (ELISA). After 48-h, ranibizumab at 0.5 mg/mL, significantly induced cell death under serum-free culture conditions (p 0.05). Ranibizumab caused significant reduction of collagen type 1 alpha 1 (COL1A1) mRNA, but not for fibronectin (FN). Meanwhile, COL1A1 and FN protein levels were found upregulated in treated monolayers compared to control monolayers. Ranibizumab at 0.5 mg/mL significantly reduced cell viability in cultured HTF. From this study, we found that single application of ranibizumab is inadequate to induce the anti-fibrotic effects on HTF, suggesting the importance of adjunctive therapy. Further studies are underway to understand mechanism of actions of ranibizumab on HTF.
- Published
- 2014
- Full Text
- View/download PDF