Diabetic kidney disease (DKD) is the leading cause of end-stage renal disease. Neutrophil extracellular traps (NETs) are a network structure composed of loose chromatin and embedded with multiple proteins. Here, we observed increased NETs deposition in the glomeruli of DKD patients and diabetic mice (streptozotocin-induced or db/db mice). After NETs were degraded with DNase I, diabetic mice exhibited attenuated glomerulopathy and glomerular endothelial cells (GECs) injury. We also observed alleviated glomerulopathy and GECs injury in peptidylarginine deiminase 4-knockout mice with streptozotocin-induced diabetes. In vitro, NETs-induced GECs pyroptosis was characterized by pore formation in the cell membrane, dysregulation of multiple genes involved in cell membrane function, and increased expression of pyroptosis-related proteins. Strengthening the GECs surface charge by oleylamine significantly inhibited NETs-induced GECs pyroptosis. These findings suggest that the GECs charge-related pyroptosis is involved in DKD progression, which is promoted by NETs.
Keyphrases
- high glucose
- endothelial cells
- diabetic rats
- end stage renal disease
- chronic kidney disease
- oxidative stress
- type diabetes
- peritoneal dialysis
- nlrp inflammasome
- drug induced
- poor prognosis
- diabetic nephropathy
- high fat diet
- transcription factor
- dna methylation
- dna damage
- vascular endothelial growth factor
- prognostic factors
- long non coding rna
- solar cells
- wild type