Incipient renal transplant dysfunction associates with tubular syndecan-1 expression and shedding

Am J Physiol Renal Physiol. 2015 Jul 15;309(2):F137-45. doi: 10.1152/ajprenal.00127.2015. Epub 2015 May 13.

Abstract

Syndecan-1 is a transmembrane heparan sulfate proteoglycan involved in regenerative growth and cellular adhesion. We hypothesized that the induction of tubular syndecan-1 is a repair response to incipient renal damage in apparently stable, uncomplicated renal transplant recipients. We quantified tubular syndecan-1 in unselected renal protocol biopsies taken 1 yr after transplantation. Spearman rank correlation analysis revealed an inverse correlation between tubular syndecan-1 expression and creatinine clearance at the time of biopsy (r = -0.483, P < 0.03). In a larger panel of protocol and indication biopsies from renal transplant recipients, tubular syndecan-1 correlated with tubular proliferation marker Ki67 (r = 0.518, P < 0.0001). In a rat renal transplantation model, 2 mo after transplantation, mRNA expression of syndecan-1 and its major sheddase, A disintegrin and metalloproteinase-17, were upregulated (both P < 0.03). Since shed syndecan-1 might end up in the circulation, in a stable cross-sectional human renal transplant population (n = 510), we measured plasma syndecan-1. By multivariate regression analysis, we showed robust independent associations of plasma syndecan-1 with renal (plasma creatinine and plasma urea) and endothelial function parameters (plasma VEGF-A, all P < 0.01). By various approaches, we were not able to localize syndecan-1 in vessel wall or endothelial cells, which makes shedding of syndecan-1 from the endothelial glycocalyx unlikely. Our data suggest that early damage in transplanted kidneys induces repair mechanisms within the graft, namely, tubular syndecan-1 expression for tubular regeneration and VEGF production for endothelial repair. Elevated plasma syndecan-1 levels in renal transplantation patients might be interpreted as repair/survival factor related to loss of tubular and endothelial function in transplanted kidneys.

Keywords: kidney function; renal biopsies; renal transplantation; syndecan-1; vascular endothelial growth factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM Proteins / metabolism
  • ADAM17 Protein
  • Adult
  • Aged
  • Animals
  • Biomarkers / blood
  • Cohort Studies
  • Cross-Sectional Studies
  • Female
  • Humans
  • Kidney Transplantation / adverse effects*
  • Kidney Tubules / metabolism*
  • Male
  • Mice, Inbred C57BL
  • Middle Aged
  • Rats, Inbred WF
  • Renal Insufficiency / etiology
  • Renal Insufficiency / metabolism*
  • Syndecan-1 / blood*
  • Vascular Endothelial Growth Factor A / blood

Substances

  • Biomarkers
  • Syndecan-1
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • ADAM Proteins
  • ADAM17 Protein