Human Renal Fibroblasts, but Not Renal Epithelial Cells, Induce IL-1β Release during a Uropathogenic Escherichia coli Infection In Vitro

Cells. 2021 Dec 13;10(12):3522. doi: 10.3390/cells10123522.

Abstract

Understanding how uropathogenic Escherichia coli (UPEC) modulates the immune response in the kidney is essential to prevent UPEC from reaching the bloodstream and causing urosepsis. The purpose of this study was to elucidate if renal fibroblasts can release IL-1β during a UPEC infection and to investigate the mechanism behind the IL-1β release. We found that the UPEC strain CFT073 induced an increased IL-1β and LDH release from renal fibroblasts, but not from renal epithelial cells. The UPEC-induced IL-1β release was found to be NLRP3, caspase-1, caspase-4, ERK 1/2, cathepsin B and serine protease dependent in renal fibroblasts. We also found that the UPEC virulence factor α-hemolysin was necessary for IL-1β release. Conditioned medium from caspase-1, caspase-4 and NLRP3-deficient renal fibroblasts mediated an increased reactive oxygen species production from neutrophils, but reduced UPEC phagocytosis. Taken together, our study demonstrates that renal fibroblasts, but not renal epithelial cells, release IL-1β during a UPEC infection. This suggest that renal fibroblasts are vital immunoreactive cells and not only structural cells that produce and regulate the extracellular matrix.

Keywords: IL-1β; UPEC; UTI; human renal fibroblasts; inflammasome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caspase 1 / genetics
  • Caspases, Initiator / genetics
  • Cathepsin B / genetics
  • Epithelial Cells / metabolism
  • Epithelial Cells / microbiology
  • Escherichia coli Infections / genetics*
  • Escherichia coli Infections / microbiology
  • Escherichia coli Infections / pathology
  • Extracellular Matrix / genetics
  • Fibroblasts / metabolism
  • Fibroblasts / microbiology
  • Gene Expression Regulation / genetics
  • Humans
  • Interleukin-1beta / genetics*
  • Kidney / metabolism*
  • Kidney / microbiology
  • Kidney / pathology
  • MAP Kinase Signaling System / genetics
  • NLR Family, Pyrin Domain-Containing 3 Protein / genetics
  • Neutrophils / metabolism
  • Serine Proteases / genetics
  • Urinary Tract Infections / genetics*
  • Urinary Tract Infections / microbiology
  • Urinary Tract Infections / pathology
  • Uropathogenic Escherichia coli / genetics
  • Uropathogenic Escherichia coli / pathogenicity

Substances

  • IL1B protein, human
  • Interleukin-1beta
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Serine Proteases
  • CASP4 protein, human
  • Caspases, Initiator
  • Cathepsin B
  • Caspase 1