Albumin stimulates renal tubular inflammation through an HSP70-TLR4 axis in mice with early diabetic nephropathy

Dis Model Mech. 2015 Oct 1;8(10):1311-21. doi: 10.1242/dmm.019398. Epub 2015 Aug 6.

Abstract

Increased urinary albumin excretion is not simply an aftermath of glomerular injury, but is also involved in the progression of diabetic nephropathy (DN). Whereas Toll-like receptors (TLRs) are incriminated in the renal inflammation of DN, whether and how albumin is involved in the TLR-related renal inflammatory response remains to be clarified. Here, we showed that both TLR2 and TLR4, one of their putative endogenous ligands [heat shock protein 70 (HSP70)] and nuclear factor-κB promoter activity were markedly elevated in the kidneys of diabetic mice. A deficiency of TLR4 but not of TLR2 alleviated albuminuria, tubulointerstitial fibrosis and inflammation induced by diabetes. The protection against renal injury in diabetic Tlr4(-/-) mice was associated with reduced tubular injuries and preserved cubilin levels, rather than amelioration of glomerular lesions. In vitro studies revealed that albumin, a stronger inducer than high glucose (HG), induced the release of HSP70 from proximal tubular cells. HSP70 blockade ameliorated albumin-induced inflammatory mediators. HSP70 triggered the production of inflammatory mediators in a TLR4-dependent manner. Moreover, HSP70 inhibition in vivo ameliorated diabetes-induced albuminuria, inflammatory response and tubular injury. Finally, we found that individuals with DN had higher levels of TLR4 and HSP70 in the dilated tubules than non-diabetic controls. Thus, activation of the HSP70-TLR4 axis, stimulated at least in part by albumin, in the tubular cell is a newly identified mechanism associated with induction of tubulointerstitial inflammation and aggravation of pre-existing microalbuminuria in the progression of DN.

Keywords: Albuminuria; Damage-associated molecular pattern (DAMP); Diabetic nephropathy; Toll-like receptor; Tubular injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albumins / metabolism*
  • Albuminuria / complications
  • Animals
  • Apoptosis / drug effects
  • Biopsy
  • Diabetic Nephropathies / complications*
  • Diabetic Nephropathies / metabolism
  • Diabetic Nephropathies / pathology
  • Glucose / pharmacology
  • HEK293 Cells
  • HMGB1 Protein / metabolism
  • HSP70 Heat-Shock Proteins / metabolism*
  • Humans
  • Inflammation / complications*
  • Inflammation / metabolism
  • Inflammation / pathology
  • Inflammation Mediators / metabolism
  • Kidney Tubules, Proximal / metabolism*
  • Kidney Tubules, Proximal / pathology*
  • LLC-PK1 Cells
  • Mice, Inbred C57BL
  • NF-kappa B / metabolism
  • Signal Transduction / drug effects
  • Swine
  • Toll-Like Receptor 2 / metabolism
  • Toll-Like Receptor 4 / deficiency
  • Toll-Like Receptor 4 / metabolism*
  • Up-Regulation / drug effects

Substances

  • Albumins
  • HMGB1 Protein
  • HSP70 Heat-Shock Proteins
  • Inflammation Mediators
  • NF-kappa B
  • Tlr2 protein, mouse
  • Tlr4 protein, mouse
  • Toll-Like Receptor 2
  • Toll-Like Receptor 4
  • Glucose