Interleukin‑6 induces epithelial‑mesenchymal transition in human intrahepatic biliary epithelial cells

Mol Med Rep. 2016 Feb;13(2):1563-9. doi: 10.3892/mmr.2015.4706. Epub 2015 Dec 22.

Abstract

The aim of the present study was to determine the role of interleukin-6 (IL-6) in the epithelial-mesenchymal transition (EMT) of human intrahepatic biliary epithelial cell (HIBEC) lines in vitro. HIBECs were stimulated with IL-6 at concentrations of 0, 10, 20, 50 and 100 µg/l for 24 h. A wound healing and Transwell assay were performed to determine the migratory and invasive capacity of HIBECs, respectively. Following 24 h of incubation, IL-6 at 10 and 20 µg/l significantly increased the number of migrated and invaded cells (P<0.05), while stimulation with 50 and 100 µg/l IL-6 resulted in a further increase of the migratory and invasive capacity compared to that in all other groups (P<0.05). Furthermore, reverse-transcription quantitative polymerase chain reaction and western blot analyses were used to detect the mRNA and protein expression of EMT markers E-cadherin and vimentin in HIBECs. Decreased mRNA levels of E-cadherin accompanied by higher mRNA levels of vimentin were observed in the 10, 20, 50, 100 µg/l IL-6 groups compared to those in the 0 µg/l group (all P<0.05). Furthermore, the protein expression of E-cadherin was decreased, while that of vimentin was increased in the 50 and 100 µg/l IL-6 groups compared to those in the 0, 10 and 20 µg/l IL-6 groups (all P<0.05). The present study therefore indicated that IL-6 promoted the process of EMT in HIBECs as characterized by increased migration and invasion of HIBECs and the typical changes in mRNA and protein expression of the EMT markers E-cadherin and vimentin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bile Ducts, Intrahepatic / drug effects
  • Bile Ducts, Intrahepatic / metabolism
  • Bile Ducts, Intrahepatic / pathology
  • Cadherins / biosynthesis*
  • Cell Movement
  • Epithelial Cells / drug effects
  • Epithelial Cells / pathology
  • Epithelial-Mesenchymal Transition / drug effects*
  • Gene Expression Regulation
  • Humans
  • Interleukin-6 / administration & dosage*
  • Interleukin-6 / metabolism
  • Neoplasm Invasiveness / pathology
  • RNA, Messenger / biosynthesis
  • Vimentin / biosynthesis*

Substances

  • Cadherins
  • IL6 protein, human
  • Interleukin-6
  • RNA, Messenger
  • Vimentin