Astragaloside III activates TACE/ADAM17-dependent anti-inflammatory and growth factor signaling in endothelial cells in a p38-dependent fashion

Phytother Res. 2020 May;34(5):1096-1107. doi: 10.1002/ptr.6603. Epub 2020 Mar 20.

Abstract

Astragaloside III (AS-III) is a triterpenoid saponin contained in Astragali Radix and has potent anti-inflammatory effects on vascular endothelial cells; however, underlying mechanisms are unclear. In this study, we provided the first piece of evidence that AS-III induced phosphorylation of TNF-α converting enzyme (TACE) at Thr735 and enhanced its sheddase activity. As a result, AS-III reduced surface TNFR1 level and increased content of sTNFR1 in the culture media, leading to the inhibition of NF-κB signaling pathway and attenuation of downstream cytokine gene expression. Furthermore, AS-III induced TACE-dependent epidermal growth factor receptor (EGFR) transactivation and activation of downstream ERK1/2 and AKT pathways. Finally, AS-III induced activation of p38. Both TACE activation and EGFR transactivation induced by AS-III were significantly inhibited by p38 inhibitor SB203580. Taken together, we concluded that AS-III activates TACE-dependent anti-inflammatory and growth factor signaling in vascular endothelial cells in a p38-dependent fashion, which may contribute to its cardiovascular protective effect.

Keywords: Astragaloside III; TNF-α converting enzyme; TNFR1; epidermal growth factor receptor; p38; vascular endothelial cells.

MeSH terms

  • ADAM17 Protein / drug effects*
  • Animals
  • Endothelial Cells / drug effects*
  • Humans
  • Mice
  • Saponins / pharmacology
  • Saponins / therapeutic use*
  • Signal Transduction / drug effects

Substances

  • Saponins
  • ADAM17 Protein
  • astragaloside III