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Journal: The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology
Article Title: Sildenafil suppresses the activation of hypertrophic scar fibroblasts by promoting the KLF15-mediated inhibition of LOXL1 transcription
doi: 10.4196/kjpp.25.179
Figure Lengend Snippet: KLF15 knockdown canceled the effect of SIL on proliferation, migration, and ECM deposition in HSFbs. HSFbs were treated with TGF-β1 (5 ng/ml), SIL (100 µM) and/or KT5823 (1 µM) for 24 h. (A) KLF15 mRNA expression was detected using RT-qPCR. (B) KLF15 protein levels were assessed using Western blotting assays. (C, D) HSFbs were treated with a negative control short hairpin (sh) RNA ( sh-NC) , or shRNAs targeting KLF15 ( sh-KLF15#1 or sh-KLF15#2 ) for 48 h. KLF15 mRNA expression was detected using RT-qPCR (C). KLF15 protein levels were examined using Western blotting assays (D). (E–H) HSFbs were treated with TGF-β1 (5 ng/ml), SIL (100 µM) co-incubated 5 ng/ml TGF-β1, SIL combined with a sh-NC and 5 ng/ml TGF-β1, or SIL combined with a KLF15- targeting shRNA and 5 ng/ml TGF-β1. (E) Cell viability was examined using CCK-8 assays. (F) Cell proliferation was detected using EdU assays. Scale bar = 100 µM. (G) Cell migration was assessed using transwell assays. Scale bar = 100 µM. (H) The expression of collagen I, fibronectin, and α-SMA was detected by Western blotting assays. Data are presented as the mean ± SD. All experiments were performed on three independent occasions. KLF15, Krüppel-like factor 15; SIL, sildenafil; ECM, extracellular matrix; HSFbs, hypertrophic scarring-derived fibroblasts; TGF-β1, transforming growth factor beta 1; CCK-8, Cell Counting Kit-8; EdU, 5-ethynyl-2′-deoxyuridine; α-SMA, alpha smooth muscle actin. *p < 0.05, **p < 0.01, ***p < 0.001.
Article Snippet: The cells were treated with 5 ng/ml TGF-β1 (100-21C; Peprotech) for 24 h. According to experimental groups, cells were co-treated with 10, 20, 50, and 100 μM
Techniques: Knockdown, Migration, Expressing, Quantitative RT-PCR, Western Blot, Negative Control, Incubation, shRNA, CCK-8 Assay, Derivative Assay, Cell Counting