TGF-β-induced activation of conjunctival fibroblasts is modulated by FGF-2 and substratum stiffness.

Autor: Matsumura, Tomoyo, Fujimoto, Tomokazu, Futakuchi, Akiko, Takihara, Yuji, Watanabe-Kitamura, Fumika, Takahashi, Eri, Inoue-Mochita, Miyuki, Tanihara, Hidenobu, Inoue, Toshihiro
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Zdroj: PLoS ONE; 11/18/2020, Vol. 15 Issue 11, p1-15, 15p
Abstrakt: Purpose: This study aimed to investigate the effects of substratum stiffness on the sensitivity of human conjunctival fibroblasts to transforming growth factor (TGF)-β, and to explore the molecular mechanism of action. Methods: Human conjunctival fibroblasts were cultured on collagen-coated plastic or silicone plates. The stiffness of the silicone plates was 0.2 or 64 kPa. Cells were treated by 2.5 ng/mL TGF-β2 with or without fibroblast growth factor (FGF)-2 (0–100 ng/mL) for 24 h or 48 h. The protein expression levels were determined by Western blot analysis. Cell proliferation was assessed using the WST-8 assay. Results: FGF-2 suppressed the TGF-β-induced expression of α-smooth muscle actin (SMA) and collagen type I (Col I), but not fibronectin (FN). Both FGF-2 and TGF-β2 increased cell proliferation without an additive effect. The induction of α-SMA by TGF-β2 was decreased on the soft substratum, without any change in the expression level or subcellular location of Yes-associated protein/transcriptional coactivator with PDZ-binding motif (YAP/TAZ). FGF-2 suppressed TGF-β-induced α-SMA expression even on the soft substratum. Conclusions: FGF-2 treatment and a soft substratum suppressed TGF-β-induced transdifferentiation of conjunctival fibroblasts into myofibroblasts. FGF-2 attenuated the TGF-β-induced expression of α-SMA, even on a soft substratum. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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