Diabetologia

, Volume 37, Issue 3, pp 313–320

Expression of glomerular extracellular matrix components in human diabetic nephropathy: decrease of heparan sulphate in the glomerular basement membrane

Authors

  • J. T. Tamsma
    • Department of PathologyUniversity Hospital Leiden
  • J. van den Born
    • Department of NephrologyUniversity Hospital Nijmegen
  • J. A. Bruijn
    • Department of PathologyUniversity Hospital Leiden
  • K. J. M. Assmann
    • Department of PathologyUniversity Hospital Nijmegen
  • J. J. Weening
    • Department of PathologyUniversity of Groningen
    • Department of PathologyUniversity of Amsterdam
  • J. H. M. Berden
    • Department of NephrologyUniversity Hospital Nijmegen
  • J. Wieslander
    • Department of Autoimmune SerologyStatens Seruminstitut
  • E. Schrama
    • Department of NephrologyUniversity Hospital Leiden
  • J. Hermans
    • Department of Medical StatisticsUniversity of Leiden
  • J. H. Veerkamp
    • Department of BiochemistryUniversity of Nijmegen
  • H. H. P. J. Lemkes
    • Department of PathologyUniversity Hospital Leiden
  • F. J. van der Woude
    • Department of PathologyUniversity Hospital Leiden
Originals

DOI: 10.1007/BF00398060

Cite this article as:
Tamsma, J.T., van den Born, J., Bruijn, J.A. et al. Diabetologia (1994) 37: 313. doi:10.1007/BF00398060

Summary

Diabetic nephropathy is characterized by albuminuria which proceeds to overt proteinuria. The highly negatively stained HS side chain of heparan sulphate proteoglycan (HSPG) is a major determinant of the charge-dependent permeability of the GBM. We set out to study the presence of HS and HSPG in the GBM of patients with diabetic nephropathy using newly developed monoclonal antibodies, and to compare HSPG expression to the expression of other previously investigated glomerular extracellular matrix compounds. Immunohistochemically, glomerular extracellular matrix components were analysed in 14 renal biopsies of patients with diabetic nephropathy and compared with those of normal control subjects. Monoclonal antibodies used were: JM403 against the HS side chain of GBM HSPG and JM72 against the HSPG-core protein. Also, a polyclonal antiserum (B31) against human GBM-HSPG-core protein was used. Additionally, antibodies were used against collagen types I, III, IV and against α1(IV)NC, α3(IV)NC and fibronectin. Staining was scored for intensity and for staining pattern by four independent observers who had no previous knowledge of the sample origin. No glomerular staining was seen for collagen type I. Collagen type III was present in some diabetic nodules. Anti-collagen type IV showed a decreased GBM staining in patients with diabetic nephropathy (p = 0.04). With anti-α1(IV)NC no changes in GBM staining intensity were observed; with anti-α3(IV)NC brilliant GBM staining was seen in both groups. Increased mesangial staining (p = 0.003) was seen with anti-collagen type IV in biopsies with nodular lesions. No differences were observed for fibronectin although it was abundantly present in the mesangial area of biopsies from patients with diabetic nephropathy. In biopsies with mesangial expansion and in biopsies with diabetic nodules, we observed a decreased GBM (p = 0.001) HS side chain staining (JM403) without changes in HSPG-core protein staining (JM72,B31). The HS staining pattern regularly changed from a linear to a more granular and irregular pattern. In patients with a creatinine clearance of more than 15 ml/min, the intensity of GBM HS staining showed an inverse correlation with the rate of proteinuria (r = -0.85, p = 0.004), suggesting a functional relationship. The decreased HS staining in the GBM may reflect the potentially disrupted charge barrier in diabetic nephropathy.

Key words

Diabetic nephropathyheparan sulphateheparan sulphate proteoglycanglomerular basement membraneextracellular matrix

Abbreviations

HS

Heparan sulphate

GBM

glomerular basement membrane

HSPG

heparan sulphate proteoglycan

NC

noncollagenous globular domain

IDDM

insulin-dependent diabetes mellitus

NIDDM

non-insulin-dependent diabetes mellitus

Copyright information

© Springer-Verlag 1994