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Reactive Oxygen Species Modulate the Barrier Function of the Human Glomerular Endothelial Glycocalyx

Singh, A. (author)
Ramnath, R. D. (author)
Foster, R. R. (author)
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Wylie, E. C. (author)
Fridén, Vincent, 1975 (author)
Gothenburg University,Göteborgs universitet,Institutionen för medicin,Institute of Medicine
Dasgupta, I. (author)
Haraldsson, Börje, 1957 (author)
Gothenburg University,Göteborgs universitet,Institutionen för medicin,Institute of Medicine
Welsh, G. I. (author)
Mathieson, P. W. (author)
Satchell, S. C. (author)
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 (creator_code:org_t)
2013-02-14
2013
English.
In: Plos One. - : Public Library of Science (PLoS). - 1932-6203. ; 8:2
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Reactive oxygen species (ROS) play a key role in the pathogenesis of proteinuria in glomerular diseases like diabetic nephropathy. Glomerular endothelial cell (GEnC) glycocalyx covers the luminal aspect of the glomerular capillary wall and makes an important contribution to the glomerular barrier. ROS are known to depolymerise glycosaminoglycan (GAG) chains of proteoglycans, which are crucial for the barrier function of GEnC glycocalyx. The aim of this study is to investigate the direct effects of ROS on the structure and function of GEnC glycocalyx using conditionally immortalised human GEnC. ROS were generated by exogenous hydrogen peroxide. Biosynthesis and cleavage of GAG chains was analyzed by radiolabelling (S35 and 3H-glucosamine). GAG chains were quantified on GEnC surface and in the cell supernatant using liquid chromatography and immunofluorescence techniques. Barrier properties were estimated by measuring trans-endothelial passage of albumin. ROS caused a significant loss of WGA lectin and heparan sulphate staining from the surface of GEnC. This lead to an increase in trans-endothelial albumin passage. The latter could be inhibited by catalase and superoxide dismutase. The effect of ROS on GEnC was not mediated via the GAG biosynthetic pathway. Quantification of radiolabelled GAG fractions in the supernatant confirmed that ROS directly caused shedding of HS GAG. This finding is clinically relevant and suggests a mechanism by which ROS may cause proteinuria in clinical conditions associated with high oxidative stress.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine (hsv//eng)

Keyword

cardiovascular-disease
heparan-sulfate
hydrogen-peroxide
oxidative
stress
cell glycocalyx
in-vitro
permeability
proteinuria
kidney
glycosaminoglycans

Publication and Content Type

ref (subject category)
art (subject category)

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