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European Journal of Cardio-Thoracic Surgery, Vol 10, 676-683, Copyright © 1996 by European Association for Cardio-thoracic Surgery
AH Chester, JA Borland, PM Taylor, ML Rose and MH Yacoub
OBJECTIVE: The performance of coronary bypass grafts can be affected by a
variety of circulating cell types. The initial event in any biological
effect of such cells is adherence to the vascular endothelium prior to
migration into the perivascular space. We aimed to investigate the
expression of molecules that regulate cell adhesion in blood vessels
employed as bypass conduits. METHODS: Segments of human saphenous vein,
internal mammary artery, gastroepiploic artery and inferior epigastric
artery were stained using specific monoclonal antibodies against the
endothelial workers EN-4, Pal-E, von Willebrand factor small (vWF), and the
cell adhesion molecules platelet- endothelium cell adhesion molecule
(PECAM), intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion
molecule-1 (VCAM-1), E- selectin, the leucocyte marker (CD45) and major
histocompatibility complex (MHC) class I and II antigens, with
visualisation by ABC immunoperoxidase method. RESULTS: All vessels had a
strong expression of the endothelial specific antigens EN4, vWF, and PECAM
as well as MHC class I. However, there was less expression of Pal-E,
ICAM-1, E- Selectin and of the DR determinant of MHC class II. VCAM-1, DP
and DQ determinants of MHC class II were expressed to a weaker extent.
There were no marked differences in the expression of all the molecules
examined between the four vessel types. CONCLUSION: Thus vessels used as
bypass grafts are immunogenic and possess the potential to attract and
interact with blood elements. Definition of the molecules responsible could
offer opportunities for modulating the response to such interactions.
ARTICLES
Vascular adhesion molecules and immunogenicity in blood vessels used as coronary artery bypass grafts
Department of Cardiothoracic Surgery, Imperial College of Science, Technology and Medicine, National Heart and Lung Institute, Harefield Hospital, Middlesex, UK.
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