Irradiation Activates MZF1 to Inhibit miR-541-5p Expression and Promote Epithelial-Mesenchymal Transition (EMT) in Radiation-Induced Pulmonary Fibrosis (RIPF) by Upregulating Slug

Int J Mol Sci. 2021 Oct 20;22(21):11309. doi: 10.3390/ijms222111309.

Abstract

Understanding miRNAs regulatory roles in epithelial-mesenchymal transition (EMT) would help establish new avenues for further uncovering the mechanisms underlying radiation-induced pulmonary fibrosis (RIPF) and identifying preventative and therapeutic targets. Here, we demonstrated that miR-541-5p repression by Myeloid Zinc Finger 1 (MZF1) promotes radiation-induced EMT and RIPF. Irradiation could decrease miR-541-5p expression in vitro and in vivo and inversely correlated to RIPF development. Ectopic miR-541-5p expression suppressed radiation-induced-EMT in vitro and in vivo. Knockdown of Slug, the functional target of miR-541-5p, inhibited EMT induction by irradiation. The upregulation of transcription factor MZF1 upon irradiation inhibited the expression of endogenous miR-541-5p and its primary precursor (pri-miR-541-5p), which regulated the effect of the Slug on the EMT process. Our finding showed that ectopic miR-541-5p expression mitigated RIPF in mice by targeting Slug. Thus, irradiation activates MZF1 to downregulate miR-541-5p in alveolar epithelial cells, promoting EMT and contributing to RIPF by targeting Slug. Our observation provides further understanding of the development of RIPF and determines potential preventative and therapeutic targets.

Keywords: EMT; MZF1; miR-541-5p; radiation-induced pulmonary fibrosis; slug.

MeSH terms

  • A549 Cells
  • Alveolar Epithelial Cells / metabolism
  • Animals
  • Cell Line, Tumor
  • Epithelial-Mesenchymal Transition / genetics
  • Epithelial-Mesenchymal Transition / radiation effects*
  • Humans
  • Kruppel-Like Transcription Factors / genetics
  • Kruppel-Like Transcription Factors / metabolism
  • Lung / metabolism
  • Lung / physiology
  • Lung Injury / physiopathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Pulmonary Fibrosis / genetics*
  • Pulmonary Fibrosis / metabolism
  • Radiation Fibrosis Syndrome / genetics
  • Signal Transduction / physiology
  • Snail Family Transcription Factors / genetics
  • Snail Family Transcription Factors / metabolism
  • Transcription Factors / metabolism

Substances

  • Kruppel-Like Transcription Factors
  • MIRN541 microRNA, mouse
  • MicroRNAs
  • Mzf1 protein, mouse
  • Snai2 protein, mouse
  • Snail Family Transcription Factors
  • Transcription Factors