Abstract | BACKGROUND: METHODS: Dermal fibroblasts obtained from one female patient aged 21 years were maintained in Dulbecco's modified Eagle's medium. Cells (<6 passages) were treated with or without Smad3 siRNA and the expression levels of related genes were examined by Reverse Transcription Polymerase Chain Reaction (RT-PCR) and Western Blot. Statistical analysis was performed using one-way ANOVA (Dunnett correction) and the Excel 7.0 software, with significance set at p<0.05. RESULTS: The knockdown of Smad3 expression in mRNA and protein levels was confirmed using RT-PCR and Western Blot. Compared to blank, the mRNA levels of types I and III procollagen were also significantly and uniquely decreased following the reduction of Smad3 by siRNA (p<0.05). The results indicate that Smad3 plays an important role in the TGF-beta induced fibrosis in keloid. Downregulation of Smad3 expression in keloid fibroblasts can significantly decrease procollagen gene expression. SiRNA targeting Smad3 was an efficient reagent to reduce ECM deposition and attenuate process of fibrosis. It could be a new promising therapeutic approach to improve skin wound healing and inhibit progression of fibrotic conditions by interrupting the TGF-beta signal pathway.
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Authors | Zimin Wang, Zhongyu Gao, Yi Shi, Yi Sun, Zihao Lin, Hua Jiang, Tiesheng Hou, Qiugen Wang, Xiangbin Yuan, Xiaohai Zhu, Hong Wu, Youxin Jin |
Journal | Journal of plastic, reconstructive & aesthetic surgery : JPRAS
(J Plast Reconstr Aesthet Surg)
Vol. 60
Issue 11
Pg. 1193-9
( 2007)
ISSN: 1748-6815 [Print] Netherlands |
PMID | 17889631
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Collagen Type I
- Collagen Type III
- RNA, Small Interfering
- SMAD3 protein, human
- Smad3 Protein
- Transforming Growth Factor beta
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Topics |
- Adult
- Cells, Cultured
- Collagen Type I
(biosynthesis)
- Collagen Type III
(biosynthesis)
- Female
- Fibroblasts
(metabolism)
- Humans
- Keloid
(genetics, pathology)
- RNA, Small Interfering
(pharmacology)
- Reverse Transcriptase Polymerase Chain Reaction
- Smad3 Protein
(genetics, metabolism)
- Transforming Growth Factor beta
(physiology)
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