Urinary extracellular vesicles as a monitoring tool for renal damage in patients not meeting criteria for chronic kidney disease
Year: 2024
Type: article
Study design: Observational Study
Abstract: Background: are considered at no increased cardiorenal risk. However, higher incidence of renal function decline and cardiovascular events have been shown within the normoalbuminuria range. Novel subclinical indicators may help to identify higher-risk patients. Urinary extracellular vesicles (uEVs) are sentinels of renal function non-invasively. Here we aimed to approach the early assessment of cardiorenal risk by investigating the protein cargo of uEVs. Methods: Hypertensive patients were classified in control group (C) with ACR < 10 mg/g, and high-normal group (HN) with ACR 10-30 mg/g. Isolated uEVs were characterized by western blotting and electron microscopy and the protein cargo was analyzed by untargeted proteomics (LC-MS/MS) in a first discovery cohort. Protein confirmation was performed in a different cohort by ExoView. Immunohistochemistry of human kidney biopsies was also performed to evaluate the potential of uEVs to reflect renal damage. Results: HN albuminuria does not affect the uEVs concentration, size, or tetraspanin profile. Among >6200 uEVs proteins identified, 43 define a panel significantly altered in HN patients without variation in urine, mostly annotated in the tubule (39 out of 43). The tubular transporter long-chain fatty acid transport protein 2 (SLC27A2) and the apical membrane protein amnionless (AMN) confirmed their alteration in HN patients evidencing impaired tubular reabsorption. SLC27A2 showed tubular expression and significantly reduced levels in patients with diagnostic criteria for CKD. Conclusions: Alterations in the EV-mediated molecular profile are evident before pathological ACR levels are reached. Direct quantitation of SLC27A2 and AMN in uEVs helps identifying normoalbuminuric subjects with higher cardiorenal risk in early monitoring of CKD.
Source: Journal of Extracellular Biology
DOI: 10.1002/jex2.170
Institutions: Hospital Universitario Fundación Jiménez Díaz, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Spanish National Centre for Cardiovascular Research, Centro de Investigación en Red en Enfermedades Cardiovasculares, Complejo Hospitalario Universitario de Santiago, Instituto de Investigación Sanitaria de Santiago, Research Institute Hospital 12 de Octubre, Hospital Universitario 12 De Octubre, Universidad Autónoma de Madrid, Hospital Nacional de Parapléjicos, Universidad Europea de Madrid, Universidad Complutense de Madrid
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,260
Awards: G1095970281, G1347714602, G1362434360, G1601999059, G1647210306, G1700907536, G1791132035, G186072593, G1893433196, G2524266544, G2854544501, G3049731404, G3625404409, G4327487443, G4388934595, G5123827200, G5313999542, Descifrando el metabolismo del Aneurisma Torácico Aórtico mediante imagen molecular: desde el desarrollo silente a la identificación de marcadores de diagnóstico, G588447059, G6719657080, G6728930308, G6731467812, G674909863, G8250635248, G8467630562
OpenAlex ID: W4402572807
