Human host defense peptide LL-37 facilitates double-stranded RNA pro-inflammatory signaling through up-regulation of TLR3 expression in vascular smooth muscle cells

Inflamm Res. 2020 Jun;69(6):579-588. doi: 10.1007/s00011-020-01340-2. Epub 2020 Mar 27.

Abstract

Objective: The importance of human host defense peptide LL-37 in vascular innate immunity is not understood. Here, we assess the impact of LL-37 on double-stranded RNA (dsRNA) signaling in human vascular smooth muscle cells.

Materials and methods: Cellular import of LL-37 and synthetic dsRNA (poly I:C) were investigated by immunocytochemistry and fluorescence imaging. Transcript and protein expression were determined by qPCR, ELISA and Western blot. Knockdown of TLR3 was performed by siRNA.

Results: LL-37 was rapidly internalized, suggesting that it has intracellular actions. Co-stimulation with poly I:C and LL-37 enhanced pro-inflammatory IL-6 and MCP-1 transcripts several fold compared to treatment with poly I:C or LL-37 alone. Poly I:C increased IL-6 and MCP-1 protein production, and this effect was potentiated by LL-37. LL-37-induced stimulation of poly I:C signaling was not associated with enhanced import of poly I:C. Treatment with poly I:C and LL-37 in combination increased expression of dsRNA receptor TLR3 compared to stimulation with poly I:C or LL-37 alone. In TLR3 knockdown cells, treatment with poly I:C and LL-37 in combination had no effect on IL-6 and MCP-1 expression, showing loss of function.

Conclusions: LL-37 potentiates dsRNA-induced cytokine production through up-regulation of TLR3 expression representing a novel pro-inflammatory mechanism.

Keywords: Antimicrobial peptide; Cathelicidin; Cytokines; Innate immunity; Poly I:C.

MeSH terms

  • Antimicrobial Cationic Peptides / metabolism*
  • Cathelicidins
  • Cell Survival
  • Cells, Cultured
  • Chemokine CCL2 / metabolism
  • Coronary Vessels / cytology
  • Humans
  • Inflammation / genetics
  • Inflammation / metabolism
  • Interleukin-6 / metabolism
  • Muscle, Smooth, Vascular / cytology
  • Myocytes, Smooth Muscle / metabolism*
  • Poly I-C
  • RNA, Double-Stranded / metabolism*
  • RNA, Small Interfering
  • Signal Transduction
  • Toll-Like Receptor 3 / genetics*
  • Toll-Like Receptor 3 / metabolism
  • Up-Regulation

Substances

  • Antimicrobial Cationic Peptides
  • CCL2 protein, human
  • Chemokine CCL2
  • IL6 protein, human
  • Interleukin-6
  • RNA, Double-Stranded
  • RNA, Small Interfering
  • TLR3 protein, human
  • Toll-Like Receptor 3
  • Poly I-C
  • Cathelicidins