Expression of sialidase and dystroglycan in human glomerular diseases

• Published in: Nephrology, dialysis, transplantation Vol. 25; no. 2; pp. 478 - 484
• Main Authors: Vogtländer, Nils P. J., van der Vlag, Johan, Bakker, Marinka A. H., Dijkman, Henry B., Wevers, Ron A., Campbell, Kevin P., Wetzels, Jack F. M., Berden, Jo H. M.
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.02.2010
• Subjects: Adolescent; Adult; Aged; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy; Biological and medical sciences; dystroglycan; Dystroglycans - biosynthesis; Emergency and intensive care: renal failure. Dialysis management; Female; Glomerulonephritis; Glomerulonephritis, Membranous - metabolism; Glomerulosclerosis, Focal Segmental - metabolism; Humans; Intensive care medicine; Lupus Nephritis - metabolism; Male; Medical sciences; Middle Aged; Nephrology. Urinary tract diseases; Nephropathies. Renovascular diseases. Renal failure; Nephrosis, Lipoid - metabolism; Neuraminidase - biosynthesis; podocalyxin; podocyte; sialic acid; sialidase; Young Adult; sialidase; dystroglycan; podocalyxin; sialic acid; podocyte; Kidney disease; Human; Podocyte; Extrarenal dialysis; Sialic acid; Urinary system disease; Hemodialysis; Renal failure
• ISSN: 0931-0509; 1460-2385
• DOI: 10.1093/ndt/gfp465

Background. α-Dystroglycan (α-DG) is a negatively charged glycoprotein that covers the surface of podocytes. A decreased glomerular expression of α-DG has been described in minimal change nephropathy (MCN), but not in focal segmental glomerulosclerosis (FSGS). This was suggested as a tool to distinguish these diseases. Sialic acid is a negatively charged carbohydrate extensively present on both α-DG and podocalyxin, which is also expressed on podocytes. Intrarenal perfusion with bacterial sialidase leads to foot process effacement and proteinuria. This is the first study on the expression of endogenous glomerular sialidase; furthermore, the expression of dystroglycan was re-evaluated. Methods. The expression of α-DG and sialidase was investigated by immunofluorescence in kidney biopsies of patients with MCN (n = 5), FSGS (n = 15), proliferative lupus nephritis (LN, n = 9), membranous glomerulopathy (MG, n = 10) and normal human kidneys (NHK, n = 4). The urinary sialic acid concentration was measured using a newly developed LC-tandem mass spectrometry method. Results. A 3-fold increased glomerular expression of sialidase was found in MG, accompanied with an increased urinary sialic acid concentration in two MG patients. However, we did not observe major changes in the expression of α-DG in patients with the above-mentioned glomerular diseases compared to NHK, also not between MCN and FSGS. Conclusions. Endogenous glomerular sialidase expression is increased in MG, which might represent a novel mechanism for the loss of negative charge in the glomerular capillary filter. The expression of dystroglycan cannot be used as a diagnostic tool to differentiate between glomerular diseases.