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Elevated Urine Heparanase Levels Are Associated with Proteinuria and Decreased Renal Allograft Function

Heparanase is an endo-β-glucuronidase that cleaves heparan sulfate side chains, leading to structural modifications that loosen the extracellular matrix barrier and associated with tumor metastasis, inflammation and angiogenesis. In addition, the highly sulfated heparan sulfate proteoglycans are imp...

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Autores principales: Shafat, Itay, Agbaria, Amir, Boaz, Mona, Schwartz, Doron, Baruch, Ronny, Nakash, Richard, Ilan, Neta, Vlodavsky, Israel, Weinstein, Talia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441528/
https://www.ncbi.nlm.nih.gov/pubmed/23028487
http://dx.doi.org/10.1371/journal.pone.0044076
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author Shafat, Itay
Agbaria, Amir
Boaz, Mona
Schwartz, Doron
Baruch, Ronny
Nakash, Richard
Ilan, Neta
Vlodavsky, Israel
Weinstein, Talia
author_facet Shafat, Itay
Agbaria, Amir
Boaz, Mona
Schwartz, Doron
Baruch, Ronny
Nakash, Richard
Ilan, Neta
Vlodavsky, Israel
Weinstein, Talia
author_sort Shafat, Itay
collection PubMed
description Heparanase is an endo-β-glucuronidase that cleaves heparan sulfate side chains, leading to structural modifications that loosen the extracellular matrix barrier and associated with tumor metastasis, inflammation and angiogenesis. In addition, the highly sulfated heparan sulfate proteoglycans are important constituents of the glomerular basement membrane and its permselective properties. Recent studies suggest a role for heparanase in several experimental and human glomerular diseases associated with proteinuria such as diabetes, minimal change disease, and membranous nephropathy. Here, we quantified blood and urine heparanase levels in renal transplant recipients and patients with chronic kidney disease (CKD), and assessed whether alterations in heparanase levels correlate with proteinuria and renal function. We report that in transplanted patients, urinary heparanase was markedly elevated, inversely associated with estimated glomerular filtration rate (eGFR), suggesting a relationship between heparanase and graft function. In CKD patients, urinary heparanase was markedly elevated and associated with proteinuria, but not with eGFR. In addition, urinary heparanase correlated significantly with plasma heparanase in transplanted patients. Such a systemic spread of heparanase may lead to damage of cells and tissues alongside the kidney.The newly described association between heparanase, proteinuria and decreased renal function is expected to pave the way for new therapeutic options aimed at attenuating chronic renal allograft nephropathy, leading to improved graft survival and patient outcome.
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spelling pubmed-34415282012-10-01 Elevated Urine Heparanase Levels Are Associated with Proteinuria and Decreased Renal Allograft Function Shafat, Itay Agbaria, Amir Boaz, Mona Schwartz, Doron Baruch, Ronny Nakash, Richard Ilan, Neta Vlodavsky, Israel Weinstein, Talia PLoS One Research Article Heparanase is an endo-β-glucuronidase that cleaves heparan sulfate side chains, leading to structural modifications that loosen the extracellular matrix barrier and associated with tumor metastasis, inflammation and angiogenesis. In addition, the highly sulfated heparan sulfate proteoglycans are important constituents of the glomerular basement membrane and its permselective properties. Recent studies suggest a role for heparanase in several experimental and human glomerular diseases associated with proteinuria such as diabetes, minimal change disease, and membranous nephropathy. Here, we quantified blood and urine heparanase levels in renal transplant recipients and patients with chronic kidney disease (CKD), and assessed whether alterations in heparanase levels correlate with proteinuria and renal function. We report that in transplanted patients, urinary heparanase was markedly elevated, inversely associated with estimated glomerular filtration rate (eGFR), suggesting a relationship between heparanase and graft function. In CKD patients, urinary heparanase was markedly elevated and associated with proteinuria, but not with eGFR. In addition, urinary heparanase correlated significantly with plasma heparanase in transplanted patients. Such a systemic spread of heparanase may lead to damage of cells and tissues alongside the kidney.The newly described association between heparanase, proteinuria and decreased renal function is expected to pave the way for new therapeutic options aimed at attenuating chronic renal allograft nephropathy, leading to improved graft survival and patient outcome. Public Library of Science 2012-09-13 /pmc/articles/PMC3441528/ /pubmed/23028487 http://dx.doi.org/10.1371/journal.pone.0044076 Text en © 2012 Shafat et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shafat, Itay
Agbaria, Amir
Boaz, Mona
Schwartz, Doron
Baruch, Ronny
Nakash, Richard
Ilan, Neta
Vlodavsky, Israel
Weinstein, Talia
Elevated Urine Heparanase Levels Are Associated with Proteinuria and Decreased Renal Allograft Function
title Elevated Urine Heparanase Levels Are Associated with Proteinuria and Decreased Renal Allograft Function
title_full Elevated Urine Heparanase Levels Are Associated with Proteinuria and Decreased Renal Allograft Function
title_fullStr Elevated Urine Heparanase Levels Are Associated with Proteinuria and Decreased Renal Allograft Function
title_full_unstemmed Elevated Urine Heparanase Levels Are Associated with Proteinuria and Decreased Renal Allograft Function
title_short Elevated Urine Heparanase Levels Are Associated with Proteinuria and Decreased Renal Allograft Function
title_sort elevated urine heparanase levels are associated with proteinuria and decreased renal allograft function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441528/
https://www.ncbi.nlm.nih.gov/pubmed/23028487
http://dx.doi.org/10.1371/journal.pone.0044076
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