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Oncostatin M이 피부섬유모세포의 증식과 기질생성에 미치는 영향Effect of Oncostatin M on Proliferation and Matrix Synthesis of Dermal Fibroblasts

Other Titles
Effect of Oncostatin M on Proliferation and Matrix Synthesis of Dermal Fibroblasts
Authors
전경욱임형우한승규김우경
Issue Date
2008
Publisher
대한성형외과학회
Keywords
Oncostatin M; Dermal fibroblasts; Oncostatin M; Dermal fibroblasts
Citation
Archives of Plastic Surgery, v.35, no.2, pp.115 - 120
Indexed
KCI
Journal Title
Archives of Plastic Surgery
Volume
35
Number
2
Start Page
115
End Page
120
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/124616
ISSN
2234-6163
Abstract
Purpose: Oncostatin M(OSM) is a multifunctional cytokine that belongs to the interleukin(IL)-6 family. Although there have been a number of studies that focused on the role and mechanism of OSM in various organs and tissues, there are few reports on its effect on wound healing. The final purpose of this project is to evaluate the effect of OSM on wound healing. This pilot study was designed to investigate the effect of OSM on proliferation and matrix synthesis of human dermal fibroblasts, which are the major components of the wound healing. Methods: Excess skin that was obtained from patients who underwent skin grafts, was used for this study. From this material, fibroblasts were isolated and cultured. The cultured fibroblasts were treated with one of four concentrations of OSM. The OSM concentrations used were 0, 50, 100, and 200ng/ml, respectively. After the OSM treatment, cell proliferation was determined by the MTT assay, collagen synthesis by the C1CP method, GAG levels by the Blyscan Dye method. The parameter levels of each group were compared. Results: OSM treatment increased all the components tested in the study. In particular, cell proliferation, GAG synthesis demonstrated statistically significant increases(p<0.05 in the Mann-Whitney U-test). The highest increase in all the components was obtained at a 100ng/ml concentration of OSM.Conclusion: The results of the present study indicate that OSM stimulates proliferation and matrix synthesis of human dermal fibroblast and the optimal concentration for wound healing is 100ng/mL.
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