Open AccessLarge-Scale Proteomic Assessment of Urinary Extracellular Vesicles Highlights Their Reliability in Reflecting Protein Changes in the Kidney
Author(s) -
Qi Wu,
Søren Brandt Poulsen,
Sathish K. Murali,
P. Richard Grimm,
Xiao Tong Su,
Eric Delpire,
Paul A. Welling,
David H. Ellison,
Robert A. Fenton
Publication year - 2021
Publication title -
journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.2020071035
Subject(s) - kidney , pkd1 , urinary system , nephron , microvesicles , biology , biomarker , chemistry , biochemistry , polycystic kidney disease , endocrinology , microrna , gene
Background Urinary extracellular vesicles (uEVs) are secreted into urine by cells from the kidneys and urinary tract. Although changes in uEV proteins are used for quantitative assessment of protein levels in the kidney or biomarker discovery, whether they faithfully reflect (patho)physiologic changes in the kidney is a matter of debate. Methods Mass spectrometry was used to compare in an unbiased manner the correlations between protein levels in uEVs and kidney tissue from the same animal. Studies were performed on rats fed a normal or high K + diet. Results Absolute quantification determined a positive correlation (Pearson R =0.46 or 0.45, control or high K + respectively, P 0.9), included exosome markers Tsg101 and Alix. Relative quantification highlighted a monotonic relationship between altered transporter/channel abundances in uEVs and the kidney after dietary K + manipulation. Analysis of genetic mouse models also revealed correlations between uEVs and kidney. Conclusion This large-scale unbiased analysis identifies uEV proteins that track the abundance of the parent proteins in the kidney. The data form a novel resource for the kidney community and support the reliability of using uEV protein changes to monitor specific physiologic responses and disease mechanisms.