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      Acute and chronic glomerular damage is associated with reduced CD133 expression in urinary extracellular vesicles

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          Abstract

          Extracellular vesicles released into urine (uEVs) can represent interesting biomarkers of renal cell damage. CD133, a stem/progenitor cell marker expressed by renal progenitor cells, is highly expressed in uEVs of healthy individuals. In the present study, we evaluated the level of CD133 in the uEVs of patients with acute and chronic glomerular damage by cytofluorimetric analysis. The level of CD133 + uEVs was significantly decreased in pediatric patients with acute glomerulonephritis during the acute phase of renal damage, while it was restored after the subsequent recovery. A similar decrease was also observed in patients with chronic glomerulonephritis. Moreover, CD133 + uEVs significantly declined in patients with type 2 diabetes, used as validation group, with the lowest levels in patients with albuminuria with diabetic nephropathy. Indeed, receiver-operating characteristic curve analysis indicates the ability of CD133 + uEV values to discriminate the health condition from that of glomerular disease. In parallel, a significant decrease of CD133 in renal progenitor cells and in their derived EVs was observed in vitro after cell treatment with a combination of glucose and albumin overload, mimicking the diabetic condition. These data indicate that the level of CD133 + uEVs may represent an easily accessible marker of renal normal physiology and could provide information on the “reservoir” of regenerating cells within tubules.

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          Contributors
          (View ORCID Profile)
          (View ORCID Profile)
          Journal
          American Journal of Physiology-Renal Physiology
          American Journal of Physiology-Renal Physiology
          American Physiological Society
          1931-857X
          1522-1466
          February 01 2020
          February 01 2020
          : 318
          : 2
          : F486-F495
          Affiliations
          [1 ]Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy
          [2 ]Pediatric Nephrology Unit, Regina Margherita Children's Hospital, Città della Salute e della Scienza di Torino, Turin, Italy
          [3 ]Department of Medical Sciences, University of Turin, Turin, Italy
          [4 ]Division of Nephrology Dialysis and Transplantation, Città della Salute e della Scienza di Torino, Turin, Italy
          Article
          10.1152/ajprenal.00404.2019
          31869243
          59112238-6faa-44a3-85bb-ef967e20b2db
          © 2020
          History

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