Cytokines in fluids from polycystic kidneys

Kidney Int. 1991 Apr;39(4):718-24. doi: 10.1038/ki.1991.87.

Abstract

We sought evidence of cytokine presence and interleukin-1 beta (IL-1 beta) bioactivity in 104 aerobic culture negative cyst fluids (CFs) from 13 kidneys of 13 patients with symptomatic normal to end-stage autosomal dominant polycystic kidney disease (ADPKD). ELISAs were used to detect IL-1 beta, interleukin-2 (IL-2), tumor necrosis factor alpha (TNF alpha) and stromelysin. Prostaglandin E2 (PGE2) was detected by radioimmunoassay. IL-1 beta was present in 65 of 94 (less than 20 to 419 pg/ml, TNF alpha in 54 of 75 (less than 10 to 73 pg/ml), stromelysin in 18 of 23 (less than 1.0 to 56 ng/ml), IL-2 in 7 of 23 (0.1 to 1.3 ng/ml) and PGE2 in 9 of 10 fluids (0.03 to 0.49 ng/ml). Of 51 fluids with immunoreactive IL-1 beta, 36 were mitogenic for thymocytes. IL-1 beta concentrations correlated directly with those of IL-2; IL-1 beta presence was associated with higher stimulation indices, higher mean concentrations of TNF alpha, IL-2, stromelysin, and PGE2, and with positive endotoxin assays, suggesting activation of the cytokine cascade in vivo. Cytokine, stromelysin and PGE2 concentrations did not correlate with sodium or non-sodium solute concentrations, nor with CF blood, osmolality, or endotoxin activity, indicating that differences in concentrations among fluids could not be explained by differences in water content. These data identify cytokines as candidate contributors to the morbidity and pathogenesis of ADPKD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Body Fluids / metabolism
  • Creatinine / metabolism
  • Cytokines / metabolism*
  • Dinoprostone / metabolism
  • Endotoxins / metabolism
  • Female
  • Humans
  • Interleukin-1 / metabolism
  • Interleukin-2 / metabolism
  • Male
  • Matrix Metalloproteinase 3
  • Metalloendopeptidases / metabolism
  • Middle Aged
  • Mitogens / metabolism
  • Polycystic Kidney Diseases / etiology
  • Polycystic Kidney Diseases / metabolism*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cytokines
  • Endotoxins
  • Interleukin-1
  • Interleukin-2
  • Mitogens
  • Tumor Necrosis Factor-alpha
  • Creatinine
  • Metalloendopeptidases
  • Matrix Metalloproteinase 3
  • Dinoprostone