Back to Search Start Over

Heparanase Is a Putative Mediator of Endothelial Glycocalyx Damage in COVID-19 - A Proof-of-Concept Study.

Authors :
Drost CC
Rovas A
Osiaevi I
Rauen M
van der Vlag J
Buijsers B
Salmenov R
Lukasz A
Pavenstädt H
Linke WA
Kümpers P
Source :
Frontiers in immunology [Front Immunol] 2022 Jun 10; Vol. 13, pp. 916512. Date of Electronic Publication: 2022 Jun 10 (Print Publication: 2022).
Publication Year :
2022

Abstract

Coronavirus disease 2019 (COVID-19) is a systemic disease associated with injury (thinning) of the endothelial glycocalyx (eGC), a protective layer on the vascular endothelium. The aim of this translational study was to investigate the role of the eGC-degrading enzyme heparanase (HPSE), which is known to play a central role in the destruction of the eGC in bacterial sepsis. Excess activity of HPSE in plasma from COVID-19 patients correlated with several markers of eGC damage and perfused boundary region (PBR, an inverse estimate of glycocalyx dimensions of vessels with a diameter 4-25 µm). In a series of translational experiments, we demonstrate that the changes in eGC thickness of cultured cells exposed to COVID-19 serum correlated closely with HPSE activity in concordant plasma samples (R = 0.82, P = 0.003). Inhibition of HPSE by a nonanticoagulant heparin fragment prevented eGC injury in response to COVID-19 serum, as shown by atomic force microscopy and immunofluorescence imaging. Our results suggest that the protective effect of heparin in COVID-19 may be due to an eGC-protective off-target effect.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Drost, Rovas, Osiaevi, Rauen, van der Vlag, Buijsers, Salmenov, Lukasz, Pavenstädt, Linke and Kümpers.)

Details

Language :
English
ISSN :
1664-3224
Volume :
13
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
35757776
Full Text :
https://doi.org/10.3389/fimmu.2022.916512