DSpace

DSpace at RU >    University Library >    Academic bibliography >

SFX Query

Title: Endothelial activation and induction of monocyte adhesion by nontransferrin-bound iron present in human sera.
Author(s): Kartikasari, A.E.R. (314320156)
Georgiou, N.A.
Visseren, F.L.
Kats-Renaud, J.H. van
Asbeck, B.S. van
Marx, J.J.M. (067846645)
Publication year: 2006
Document type: Article / Letter to editor
Journal: FASEB Journal
ISSN: 0892-6638
Volume: vol. 20
Issue: iss. 2
Start page: p. 353
End page: p. 355
Abstract: Nontransferrin-bound iron (NTBI) has been detected in iron overload diseases. This form of iron may exert pro-oxidant effects and modulate cellular function and inflammatory response. The present study has aimed to investigate the effects of serum NTBI on monocyte adherence to endothelium. Measured by a recently developed high-throughput fluorescence-based assay, serum NTBI was found to be higher in both homozygotes of HFE C282Y mutation of hereditary hemochromatosis (7.9+/-0.6 microM, n=9, P<0.001) and heterozygotes (4.0+/-0.5 microM, n=8, P<0.001), compared with controls (1.6+/-0.2 microM, n=21). The effects of these sera on monocyte adhesion and endothelial activation were examined. Adhesion of normal human monocytes to C282Y homozygote- and heterozygote-serum-treated human umbilical vein endothelial cells was higher (25.0+/-0.9 and 22.1+/-0.7%, respectively) compared with controls (17.6+/-0.5%, both P<0.001). For the three groups combined, the expression of adhesion molecules, ICAM-1, VCAM-1, and E-selectin, was positively correlated to NTBI levels but not to the inflammatory marker C-reactive protein. Furthermore, accumulation of intracellular labile iron and oxidative radicals within the cells due to NTBI was evidenced. Finally, counteraction of NTBI-induced endothelial activation was observed using iron chelators. These findings therefore identify a physiological function of NTBI in monocyte-endothelial interactions that may also contribute to the development of atherosclerosis and neurodegenerative diseases.
Subject: UMCN 5.1: Genetic defects of metabolism
Organization: Clinical Chemistry
UMCN Extern
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/49413

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

  DSpace Software Copyright © 2002-2011  Duraspace - Feedback