Chymase in Plasma and Urine Extracellular Vesicles: Novel Biomarkers for Primary Hypertension

Author:

Ahmad SarfarazORCID,Deep GaganORCID,Punzi Henry A,Su Yixin,Singh Sangeeta,Kumar Ashish,Mishra Shalini,Saha Amit KORCID,Wright Kendra N,VonCannon Jessica LORCID,Dell’Italia Louis JORCID,Meredith Wayne J,Ferrario Carlos MORCID

Abstract

ABSTRACTBACKGROUNDExtracellular vesicles (EVs) have emerged as a promising liquid biopsy for various diseases. For the first time, using plasma and urinary EVs, we assessed the activity of renin-angiotensin system (RAS), a central regulator of renal, cardiac, and vascular physiology, in patients with control (Group I) or uncontrolled (Group II) primary hypertension.METHODSEVs were isolated from 34 patients with history of hypertension, and characterized for size and concentration by nanoparticle tracking analyses, exosomal biomarkers by immunogold labeling coupled with transmission electron microscopy, flow cytometry and immunoblotting. EVs were analyzed for the hydrolytic activity of chymase, angiotensin converting enzyme (ACE), ACE2, and neprilysin (NEP) by HPLC.RESULTSPlasma and urinary EVs were enriched for small EVs and expressed exosomal markers (CD63, CD9, and CD81). The size of urinary EVs (but not plasma EVs) was significantly larger in Group II compared to Group I. Differential activity of RAS enzymes was observed, with significantly higher chymase activity compared to ACE, ACE2, and NEP in plasma EVs. Similarly, urinary EVs exhibited higher chymase and NEP activity compared to ACE and ACE2 activity. Importantly, compared to Group I, significantly higher chymase activity was observed in urinary EVs (p = 0.03) from Group II, while no significant difference in activity was observed for other RAS enzymes.CONCLUSIONSBioactive RAS enzymes are present in plasma and urinary EVs. Detecting chymase in plasma and urinary EVs uncovers a novel mechanism of angiotensin II-forming enzyme and could also mediate cell-cell communication and modulate signaling pathways in recipient cells.GRAPHICAL ABSTRACT

Publisher

Cold Spring Harbor Laboratory

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