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Circulation Research. 1999;84:409-416

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(Circulation Research. 1999;84:409-416.)
© 1999 American Heart Association, Inc.


Original Contribution

Homocysteine Enhances Neutrophil-Endothelial Interactions in Both Cultured Human Cells and Rats In Vivo

Nicholas P. B. Dudman, Suzanna E. Temple, Xue Wei Guo, Weiyu Fu, Michael A. Perry

From the Department of Cardiovascular Medicine (N.P.B.D., X.W.G., W.F.), University of New South Wales, Prince Henry Hospital, Sydney, Australia; Department of Endocrinology and Diabetes (S.E.T.), Sir Charles Gairdner Hospital, Nedlands, Western Australia; and School of Physiology and Pharmacology (M.A.P.), University of New South Wales, Sydney, Australia.

Correspondence to Nicholas P.B. Dudman, Department of Cardiovascular Medicine, University of New South Wales, Prince Henry Hospital, Little Bay (Sydney), New South Wales 2036, Australia. E-mail n.dudman{at}unsw.edu.au

Abstract—Despite intense investigation, mechanisms linking the development of occlusive vascular disease with elevated levels of homocysteine (HCY) are still unclear. The vascular endothelium plays a key role in regulating thrombogenesis and thrombolysis. We hypothesized that vascular lesions in individuals with elevated plasma HCY may be related to a dysfunction of the endothelium triggered by HCY. We investigated the effect of HCY on human neutrophil adhesion to and migration through endothelial monolayers. We also examined the effect of HCY on leukocyte adhesion and migration in mesenteric venules of anesthetized rats. We found that pathophysiological concentrations of HCY in vitro induce increased adhesion between neutrophils and endothelial cells. This contact results in neutrophil migration across the endothelial layer, with concurrent damage and detachment of endothelial cells. In vivo, HCY infused in anesthetized rats caused parallel effects, increasing leukocyte adhesion to and extravasation from mesenteric venules. Our results suggest that extracellular H2O2, generated by adherent neutrophils and/or endothelial cells, is involved in the in vitro endothelial cell damage. The possibility exists that leukocyte-mediated changes in endothelial integrity and function may lead to the vascular disease seen in individuals with elevated plasma HCY.


Key Words: endothelium • occlusive vascular disease • homocystinuria • hyperhomocysteinemia • leukocyte




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