Circulating extracellular vesicles from patients with valvular heart disease induce neutrophil chemotaxis via FOXO3a and the inhibiting role of dexmedetomidine

Am J Physiol Endocrinol Metab. 2020 Jul 1;319(1):E217-E231. doi: 10.1152/ajpendo.00062.2020. Epub 2020 Jun 9.

Abstract

We previously demonstrated that circulating extracellular vesicles (EVs) from patients with valvular heart disease (VHD; vEVs) contain inflammatory components and inhibit endothelium-dependent vasodilation. Neutrophil chemotaxis plays a key role in renal dysfunction, and dexmedetomidine (DEX) can reduce renal dysfunction in cardiac surgery. However, the roles of vEVs in neutrophil chemotaxis and effects of DEX on vEVs are unknown. Here, we investigated the impact of vEVs on neutrophil chemotaxis in kidneys and the influence of DEX on vEVs. Circulating EVs were isolated from healthy subjects and patients with VHD. The effects of EVs on chemokine generation, forkhead box protein O3a (FOXO3a) pathway activation and neutrophil chemotaxis on cultured human umbilical vein endothelial cells (HUVECs) and kidneys in mice and the influence of DEX on EVs were detected. vEVs increased FOXO3a expression, decreased phosphorylation of Akt and FOXO3a, promoted FOXO3a nuclear translocation, and activated the FOXO3a signaling pathway in vitro. DEX pretreatment reduced vEV-induced CXCL4 and CCL5 expression and neutrophil chemotaxis in cultured HUVECs via the FOXO3a signaling pathway. vEVs were also found to suppress Akt phosphorylation and activate FOXO3a signaling to increase plasma levels of CXCL4 and CCL5 and neutrophil accumulation in kidney. The overall mechanism was inhibited in vivo with DEX pretreatment. Our data demonstrated that vEVs induced CXCL4-CCL5 to stimulate neutrophil infiltration in kidney, which can be inhibited by DEX via the FOXO3a signaling. Our findings reveal a unique mechanism involving vEVs in inducing neutrophils chemotaxis and may provide a novel basis for using DEX in reducing renal dysfunction in valvular heart surgery.

Keywords: extracellular vesicles; forkhead box protein O3a; neutrophil chemotaxis; renal dysfunction; valvular heart surgery.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-2 Receptor Agonists / pharmacology
  • Adult
  • Animals
  • Case-Control Studies
  • Chemokine CCL5 / drug effects
  • Chemokine CCL5 / immunology
  • Chemokine CCL5 / metabolism
  • Chemotaxis, Leukocyte / drug effects
  • Chemotaxis, Leukocyte / immunology*
  • Dexmedetomidine / pharmacology
  • Extracellular Vesicles / drug effects
  • Extracellular Vesicles / immunology*
  • Extracellular Vesicles / metabolism
  • Female
  • Forkhead Box Protein O3 / drug effects
  • Forkhead Box Protein O3 / immunology
  • Forkhead Box Protein O3 / metabolism
  • Heart Valve Diseases / immunology*
  • Heart Valve Diseases / metabolism
  • Human Umbilical Vein Endothelial Cells / drug effects
  • Human Umbilical Vein Endothelial Cells / immunology*
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Inflammation
  • Kidney / drug effects
  • Kidney / immunology*
  • Kidney / metabolism
  • Male
  • Mice
  • Middle Aged
  • Neutrophils / drug effects
  • Neutrophils / immunology*
  • Phosphorylation
  • Platelet Factor 4 / drug effects
  • Platelet Factor 4 / immunology
  • Platelet Factor 4 / metabolism
  • Proto-Oncogene Proteins c-akt / drug effects
  • Proto-Oncogene Proteins c-akt / metabolism
  • Renal Insufficiency / immunology*
  • Renal Insufficiency / metabolism
  • Vasodilation

Substances

  • Adrenergic alpha-2 Receptor Agonists
  • Chemokine CCL5
  • FOXO3 protein, human
  • Forkhead Box Protein O3
  • FoxO3 protein, mouse
  • Platelet Factor 4
  • Dexmedetomidine
  • Proto-Oncogene Proteins c-akt