TWEAK/Fn14 promotes pro-inflammatory cytokine secretion in hepatic stellate cells via NF-κB/STAT3 pathways

Mol Immunol. 2017 Jul:87:67-75. doi: 10.1016/j.molimm.2017.04.003. Epub 2017 Apr 12.

Abstract

Tumor necrosis factor-like weak inducer of apoptosis (TWEAK) and its receptor fibroblast growth factor-inducible 14 (Fn14) have been associated with liver disease. Hepatic stellate cells (HSCs) play a critical role in the hepatic wound-healing response after liver injury, but there is little information available on the role of the TWEAK/Fn14 pathway in human HSCs. In this study, we explored the role of TWEAK/Fn14 in activated human HSCs. The LX-2 cells were treated with TWEAK, and the expression of pro-inflammatory cytokines was assayed by enzyme-linked immunosorbent assay (ELISA) and real-time PCR (RT-PCR). Western blotting and RT-PCR were performed to evaluate the expression of Fn14 after TWEAK stimulation. Total and phosphorylated of inhibitor-κB (I-κB), nuclear factor kappa B (NF-κB), Janus kinase 2 (JAK2), and signal transducers and activators of transcription 3 (STAT3) were examined by western blotting after TWEAK stimulation and small interfering RNA (siRNA) transfection. The result showed that TWEAK upregulated the expression of Fn14 and pro-inflammatory factors interleukin-8 (IL-8), interleukin-6 (IL-6), regulated upon activation normal T cell expressed and secreted (RANTES), and monocyte chemotactic protein-1 (MCP-1). In LX-2 cells, the pro-inflammatory cytokine secretion was closely related to the activation of the NF-κB and STAT3 pathways. Furthermore, our research showed that STAT3 and NF-κB could interact with each other, which resulted in a significant increase of pro-inflammatory cytokine secretion. The activation of NF-κB and STAT3 signalling-dependent pro-inflammatory cytokine expression may be responsible for such a novel principle and new therapeutic targets in chronic liver disease.

Keywords: Fn14; Hepatic stellate cells (HSCs); NF-kappa B (NF-κB); Pro-inflammatory cytokines; STAT3; TWEAK.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Chemokine CCL2 / metabolism
  • Cytokine TWEAK
  • Cytokines / metabolism*
  • Hepatic Stellate Cells / metabolism*
  • Humans
  • Inflammation / metabolism*
  • Interleukin-6 / metabolism
  • Interleukin-8 / metabolism
  • Janus Kinase 2 / metabolism
  • NF-kappa B / metabolism*
  • RNA, Small Interfering / genetics
  • Receptors, Tumor Necrosis Factor / metabolism*
  • STAT3 Transcription Factor / metabolism*
  • Signal Transduction / physiology
  • TWEAK Receptor
  • Tumor Necrosis Factor-alpha / metabolism
  • Tumor Necrosis Factors / metabolism*
  • Up-Regulation / physiology

Substances

  • CCL2 protein, human
  • Chemokine CCL2
  • Cytokine TWEAK
  • Cytokines
  • Interleukin-6
  • Interleukin-8
  • NF-kappa B
  • RNA, Small Interfering
  • Receptors, Tumor Necrosis Factor
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • TNFRSF12A protein, human
  • TNFSF12 protein, human
  • TWEAK Receptor
  • Tumor Necrosis Factor-alpha
  • Tumor Necrosis Factors
  • JAK2 protein, human
  • Janus Kinase 2