60
views
0
recommends
+1 Recommend
0 collections
    9
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Urinary podocalyxin is an early marker for podocyte injury in patients with diabetes: establishment of a highly sensitive ELISA to detect urinary podocalyxin

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Aims/objective

          Nephropathy, a major complication of diabetes, is the leading cause of end-stage renal disease. Recent studies have demonstrated that podocyte injury is involved in the onset of and progression to renal insufficiency. Here, we describe a novel, highly sensitive ELISA for detecting urinary podocalyxin, a glycoconjugate on the podocyte apical surface that indicates podocyte injury, particularly in the early phase of diabetic nephropathy.

          Methods

          Urine samples from patients with glomerular diseases ( n = 142) and type 2 diabetes ( n = 71) were used to quantify urinary podocalyxin by ELISA. Urine samples were obtained from 69 healthy controls for whom laboratory data were within normal values. Podocalyxin was detected in urine by immunofluorescence, immunoelectron microscopy and western blotting.

          Results

          Morphologically, urinary podocalyxin was present as a vesicular structure; western blotting showed it as a positive band at 165–170 kDa. Levels of urinary podocalyxin were elevated in patients with various glomerular diseases and patients with diabetes. In patients with diabetes, urinary podocalyxin was higher than the cut-off value in 53.8% patients at the normoalbuminuric stage, 64.7% at the microalbuminuric stage and 66.7% at the macroalbuminuric stage. Positive correlations were observed between urinary podocalyxin levels and HbA 1c, urinary β 2 microglobulin, α 1 microglobulin and urinary N-acetyl- β- d-glucosaminidase, although urinary podocalyxin levels were not correlated with other laboratory markers such as blood pressure, lipid level, serum creatinine, estimated GFR or proteinuria.

          Conclusions/interpretation

          Urinary podocalyxin may be a useful biomarker for detecting early podocyte injury in patients with diabetes.

          Electronic supplementary material

          The online version of this article (doi:10.1007/s00125-012-2661-7) contains peer-reviewed but unedited supplementary material, which is available to authorised users.

          Related collections

          Most cited references14

          • Record: found
          • Abstract: found
          • Article: not found

          From the periphery of the glomerular capillary wall toward the center of disease: podocyte injury comes of age in diabetic nephropathy.

          Nephropathy is a major complication of diabetes. Alterations of mesangial cells have traditionally been the focus of research in deciphering molecular mechanisms of diabetic nephropathy. Injury of podocytes, if recognized at all, has been considered a late consequence caused by increasing proteinuria rather than an event inciting diabetic nephropathy. However, recent biopsy studies in humans have provided evidence that podocytes are functionally and structurally injured very early in the natural history of diabetic nephropathy. The diabetic milieu, represented by hyperglycemia, nonenzymatically glycated proteins, and mechanical stress associated with hypertension, causes downregulation of nephrin, an important protein of the slit diaphragm with antiapoptotic signaling properties. The loss of nephrin leads to foot process effacement of podocytes and increased proteinuria. A key mediator of nephrin suppression is angiotensin II (ANG II), which can activate other cytokine pathways such as transforming growth factor-beta (TGF-beta) and vascular endothelial growth factor (VEGF) systems. TGF-beta1 causes an increase in mesangial matrix deposition and glomerular basement membrane (GBM) thickening and may promote podocyte apoptosis or detachment. As a result, the denuded GBM adheres to Bowman's capsule, initiating the development of glomerulosclerosis. VEGF is both produced by and acts upon the podocyte in an autocrine manner to modulate podocyte function, including the synthesis of GBM components. Through its effects on podocyte biology, glomerular hemodynamics, and capillary endothelial permeability, VEGF likely plays an important role in diabetic albuminuria. The mainstays of therapy, glycemic control and inhibition of ANG II, are key measures to prevent early podocyte injury and the subsequent development of diabetic nephropathy.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Tubular changes in early diabetic nephropathy.

            Far from being bystanders in diabetic nephropathy, changes in the proximal tubule are important for the development of progressive diabetic kidney disease. The proximal tubule is uniquely susceptible to a variety of metabolic and hemodynamic factors associated with diabetes. Renal function and prognosis correlate better with structural lesions in the tubuli and cortical interstitium than with classical glomerular changes of diabetic nephropathy. The proximal tubules show a variety of poorly characterized changes, which have led to the notion that tubular damage represents a "final common pathway" for proteinuric renal injury. However, tubular hypertrophy, reduced organic ion transport, and other tubular changes reviewed in this paper, are already apparent before the onset of proteinuria in diabetes. Indeed, increased tubuloglomerular feedback and defective uptake and lysosomal processing may independently contribute to hyperfiltration and urinary protein loss, respectively. This finding does not mean that glomerular or vascular dysfunction do not contribute to progressive nephropathy. However, although subdividing the nephron for the purposes of analysis and scientific discovery may be useful, the interactions between tubule, glomerulus, and interstitium are likely key to the understanding of complex disorders such as diabetic nephropathy. From this "holonephric" point of view, an understanding of the changes in the diabetic tubule forms an important component to the understanding of kidney disease in diabetes.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Microalbuminuria as a predictor of clinical diabetic nephropathy.

                Bookmark

                Author and article information

                Contributors
                mhara@yoshida-hosp.jp
                Journal
                Diabetologia
                Diabetologia
                Diabetologia
                Springer-Verlag (Berlin/Heidelberg )
                0012-186X
                1432-0428
                2 August 2012
                2 August 2012
                November 2012
                : 55
                : 11
                : 2913-2919
                Affiliations
                [1 ]Department of Pediatrics, Yoshida Hospital, Yoshida 32-14, Tsubame City, 959-0242 Niigata Japan
                [2 ]Department of Nephrology, University of Tsukuba, Tsukuba, Japan
                [3 ]Department of Nephrology, Juntendo University, Tokyo, Japan
                [4 ]Department of Medicine, Niigata University, Niigata, Japan
                [5 ]Research and Development Department, Denka Seiken, Gosen, Niigata Japan
                [6 ]Department of Pediatrics, School of Medicine, Kyorin University, Mitaka, Tokyo, Japan
                Article
                2661
                10.1007/s00125-012-2661-7
                3464371
                22854890
                ace91357-31ec-422a-91b2-1465fdb8cbd3
                © The Author(s) 2012
                History
                : 30 May 2012
                : 19 June 2012
                Categories
                Article
                Custom metadata
                © Springer-Verlag Berlin Heidelberg 2012

                Endocrinology & Diabetes
                podocyte,podocalyxin,glomerular capillary wall,urine biomarker,diabetic nephropathy

                Comments

                Comment on this article