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Down-Regulation of Collagen Synthesis and Matrix Metalloproteinase Expression in Myofibroblasts from Dupuytren Nodule Using Adenovirus-Mediated Relaxin Gene Therapy

Authors
Kang, Young-MiChoi, Yun-RakYun, Chae-OkPark, Jin-OhSuk, Kyung-SooKim, Hak-SunPark, Moon-SooLee, Byung-HoLee, Hwan-MoMoon, Seong-Hwan
Issue Date
Apr-2014
Publisher
WILEY
Keywords
relaxin; fibrosis; matrix metalloproteinases; Dupuytren' s disease; collagens
Citation
JOURNAL OF ORTHOPAEDIC RESEARCH, v.32, no.4, pp.515 - 523
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF ORTHOPAEDIC RESEARCH
Volume
32
Number
4
Start Page
515
End Page
523
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/25907
DOI
10.1002/jor.22535
ISSN
0736-0266
Abstract
Dupuytren's disease is a fibroproliferative connective tissue disorder characterized by contracture of the palmer fascia of the hand. Relaxin (RLN) is a multifunctional factor which contributes to the remodeling of the pelvic ligament by inhibiting fibrosis and inflammatory activities. The aim of this study was to investigate the effect of the RLN gene on the inhibition of fibrosis in myofibroblastic cells. Myofibroblast cells with adenovirus LacZ (Ad-LacZ) as a marker gene or adenovirus relaxin (Ad-RLN) as therapeutic gene showed transgene expressions in beta-galactosidase assay and Western blot analysis. Myofibroblastic cells with Ad-RLN demonstrated a 22% and 48% reduction in collagen I and III mRNA expressions respectively, a 50% decrease in MMP-1, 70% decrease in MMP-2, 80% decrease in MMP-9, and a 15% reduction in MMP-13 protein expression compared with cultures with viral control and saline control. In addition, myofibroblastic cells with Ad-RLN showed a 40% decrease in TIMP 1 and a 15% increase in TIMP 3 protein expression at 48h compared to cultures with viral control and saline control. Also, myofibroblastic cell with Ad-RLN demonstrated a 74% inhibition of fibronectin and a 52% decrease in total collagen synthesis at 48h compared with cultures with viral control and saline control. In conclusion, the RLN gene render antifibrogenic effect on myofibroblastic cells from Dupuytren's nodule via direct inhibition of collagen synthesis not through collagenolytic pathway such as MMP-1, -13, TIMP 1, and 3. Therefore relaxin can be an alternative therapeutic strategy in initial stage of Dupuytren's disease by its antifibrogenic effect. (c) 2013 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 32:515-523, 2014.
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