Background: The excessive accumulation of extracellular matrix is a hallmark of many fibrotic diseases, including the hypertrophic scar and keloid. Recent reports from this research team had shown that exogenous nitric oxide (NO) participates in the keloid formation; however, its role on the synthesis of fibrotic factor (TGF-β1, TIMP-1 and HSP47) in the keloid fibroblasts (KF) remained unclear. Objective: In this study, to better define the potential effect of exogenous NO on the expression of fibrotic factors in KF, the enhancing effect of exogenous NO, released from a NO donor, on the synthesis of fibrotic factors in KF was investigated. Methods: The seven primary KF cultures were set up to measure the effect of exogenous NO on enhancing the expression of fibrotic factor. Results: Elevation of cellular cGMP levels was observed to be induced by NO or blocked by the hydrolysis activity of phosphodiesterase (PDE) by the PDE inhibitor. The elevated levels of cellular cGMP were noted to enhance the expression of TIMP-1 and HSP47 in KF. Exogenous NO was found to significantly accelerate the production of TIMP-1 and HSP47 in the seven primary KFs with a corresponding increase in the production of TGF-β1. Conclusion: The results have led to a conclusion, that is: the excess collagen formations in the keloid lesion may be attributed to the NO/cGMP signal pathway by initiating a rapid increase in the expression of TGF-β1, TIMP-1 and HSP47 in the KF cells.
- Heat shock protein 47 (HSP47)
- Nitric oxide (NO)
- Tissue inhibitor of MMP (TIMP)-1
ASJC Scopus subject areas