N-acetyl-l-cysteine inhibits TGF-β1-induced profibrotic responses in fibroblasts

Hisatoshi Sugiura, Tomohiro Ichikawa, Xiangde Liu, Tetsu Kobayashi, Xing Qi Wang, Shin Kawasaki, Shinsaku Togo, Koichiro Kamio, Lijun Mao, Youngsoo Ann, Masakazu Ichinose, Stephen I. Rennard

研究成果: Article査読

45 被引用数 (Scopus)

抄録

Background: Excessive production of TGF-β1 plays a key role in the tissue remodeling or fibrotic process observed in bronchial asthma, chronic pulmonary disease (COPD), and idiopathic pulmonary fibrosis (IPF). TGF-β1 has been reported to decrease the intracellular glutathione level and stimulate the production of reactive oxygen species. Objectives: The aim of this study was to evaluate whether the antioxidant N-acetyl-l-cysteine (NAC) can affect TGF-β1-mediated tissue remodeling in fibroblasts or modulate the production of fibronectin and vascular endothelial growth factor (VEGF) which are believed to be important mediators of tissue repair and remodeling. Methods: To accomplish this, human fetal lung fibroblasts (HFL-1) were used to assess the effect of NAC on the TGF-β1-mediated contraction of floating gels and the TGF-β1-induced mediator production. In addition, the effect of NAC on the TGF-β1-induced differentiation to myofibroblasts was evaluated by assessing α-smooth muscle actin (α-SMA) expression. Results: NAC significantly abolished the TGF-β1-augmented gel contraction (at 3 mM, gel size 63.4 ± 2.6% vs. 39.1 ± 4.1%; p < 0.01) compared with control in a concentration-dependent manner. NAC also significantly inhibited the TGF-β1-augmented fibronectin (p < 0.01) and VEGF (p < 0.01) production in the media of both the three-dimensional gel and monolayer culture. Furthermore, NAC reversed the TGF-β1-stimulated α-SMA expression (p < 0.01). Conclusion: These results suggest that NAC can affect the TGF-β1-induced tissue remodeling or fibrotic process in vitro.

本文言語English
ページ(範囲)487-491
ページ数5
ジャーナルPulmonary Pharmacology and Therapeutics
22
6
DOI
出版ステータスPublished - 2009 12月
外部発表はい

ASJC Scopus subject areas

  • 呼吸器内科
  • 生化学、医学
  • 薬理学(医学)

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