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Antifibrotic effects of cyclosporine A on TGF‐β1–treated lung fibroblasts and lungs from bleomycin‐treated mice: role of hypoxia‐inducible factor‐1α
Author(s) -
Yamazaki Risa,
Kasuya Yoshitoshi,
Fujita Tetsuo,
Umezawa Hiroki,
Yanagihara Madoka,
Nakamura Hiroyuki,
Yoshino Ichiro,
Tatsumi Koichiro,
Murayama Toshihiko
Publication year - 2017
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.201601357r
Subject(s) - myofibroblast , bleomycin , idiopathic pulmonary fibrosis , pulmonary fibrosis , transforming growth factor , lung , fibronectin , fibrosis , cancer research , pathology , chemistry , hypoxia (environmental) , medicine , cell , chemotherapy , biochemistry , organic chemistry , oxygen
Idiopathic pulmonary fibrosis (IPF) is a chronic lung disorder that is characterized by aberrant tissue remodeling and the formation of fibroblastic foci that are composed of fibrogenic myofibroblasts. TGF‐β1 is one of the factors that are responsible for fibrosis as it promotes fibroblast to myofibroblast differentiation (FMD) and is associated with up‐regulation of α‐smooth muscle actin. Therefore, inhibition of FMD may represent an effective strategy for the treatment of IPF. Here, we describe the treatment of human lung fibroblasts (WI‐38 and HFL‐1 cells) with cyclosporine A (CsA), which reduces TGF‐β1–induced FMD via degradation of hypoxia‐inducible factor‐1α (HIF‐1α). In addition, in primary myofibroblast‐like cells that were obtained from a patient with pulmonary fibrosis, treatment with CsA and an HIF‐1α inhibitor (HIFi) decreased the expression levels of α‐smooth muscle actin and fibronectin, which indicated that CsA and HIFi promote dedifferentiation of myofibroblasts. In mice intratracheally administered CsA or HIFi at an early fibrotic stage [7, 8, and 9 d postinstillation (dpi) of bleomycin], marked alleviation of lung fibrosis was observed at 14 dpi. These results suggest that CsA exhibits antifibrotic effects by degrading HIF‐1α and that the CsA–HIF‐1α axis provides new insights into therapeutic options for the treatment of IPF.—Yamazaki, R., Kasuya, Y., Fujita, T., Umezawa, H., Yanagihara, M., Nakamura, H., Yoshino, I., Tatsumi, K., Murayama, T. Antifibrotic effects of cyclosporine A on TGF‐β1–treated lung fibroblasts and lungs from bleomycin‐treated mice: role of hypoxia‐inducible factor‐1α. FASEB J . 31, 3359–3371 (2017). www.fasebj.org