Tianjin Medical Journal ›› 2024, Vol. 52 ›› Issue (3): 231-236.doi: 10.11958/20230719

• Cell and Molecular Biology • Previous Articles     Next Articles

The effect of lncRNA FEZF1-AS1 targeting regulation of miR-200c-3p on biological behaviors of human lung fibroblasts

MAN Jun1(), GAO Yanyan1, SONG Longfei2, GAO Fusheng1,()   

  1. 1. Department of Respiratory Medicine, 2. Department of Rehabilitation Medicine, Affiliated Hospital of Weifang Medical University, Weifang 261035, China
  • Received:2023-05-19 Revised:2023-08-12 Published:2024-03-15 Online:2024-03-13
  • Contact: E-mail: gaofs888@163.com

Abstract:

Objective To investigate the effect of FEZ family zinc finger 1-antisense RNA 1 (LncRNA FEZF1-AS1) targeting regulation of miR-200c-3p expression on biological behaviors of human lung fibroblasts (HLF). Methods Transforming growth factor β1 (TGF-β1) was used to induce the transformation of HLF into myofibroblasts, which were divided into the Blank group and the model group (HLF+TGF-β1 group). According to different transfection plasmid, cells were divided into the Blank group, the TGF-β1+Si LncRNA FEZF1-AS1 NC group and the TGF-β1+Si LncRNA FEZF1-AS1 group. The protein expressions of α-SMA, Collagen Ⅰ and Vimentin were detected by Western blot assay. The expressions of LncRNA FEZF1-AS1 and miR-200c-3p were detected by quantitative real-time PCR (qRT-PCR). Cell proliferation ability was detected by CCK-8 method, migration ability was detected by cell scratch experiment and invasion ability was detected by Transwell assay. The targeting relationship between FEZF1-AS1 and miR-200c-3p was detected by dual-luciferase reporter assay. Results Compared with the Blank group, protein expressions of α-SMA, Collagen Ⅰ, Vimentin and the expression of LncRNA FEZF1-AS1 were increased in the HLF+TGF-β1 group (P<0.05), and the expression of miR-200c-3p was decreased (P<0.05). Compared with the TGF-β1+Si LncRNA FEZF1-AS1 NC group, cell proliferation, migration, invasion ability, LncRNA FEZF1-AS1 expression, protein expressions of α-SMA, Collagen Ⅰ and Vimentin were decreased in the TGF-β1+Si LncRNA FEZF1-AS1 group (P<0.05), and the expression of miR-200c-3p was increased (P<0.05). There were binding sites between miR-200c-3p and FEZF1-AS1 gene sequence. Conclusion LncRNA FEZF1-AS1 promotes the formation and progression of idiopathic pulmonary interstitial fibrosis by inhibiting miR-200c-3p.

Key words: idiopathic pulmonary interstitial fibrosis, lung fibroblasts, myofibroblasts, FEZ family zinc finger 1-antisense RNA1, microRNA-200c-3p

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