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(Circulation. 1996;93:1319-1320.)
© 1996 American Heart Association, Inc.
Articles |
From the Department of Surgery, University of Washington School of Medicine, Seattle.
Correspondence to Alexander W. Clowes, MD, Department of Surgery, University of Washington School of Medicine, BB442 HSB, Box 356410, Seattle, WA 98195-6410.
Key Words: Editorials plasminogen activators vessels genes endothelium
| Introduction |
|---|
A great deal of effort has been put into making materials with
nonthrombotic and nonanticoagulant surfaces. Although these materials
are relatively inert in the short term, they are soon modified by the
deposition of proteins from the blood, and they do not necessarily form
smooth junctions with the adjacent arteries. One way to improve their
performance is to encourage the formation of a surface on the
biomaterial that mimics the surface of a normal vessel. Most
investigators would consider a monolayer of endothelial
cells as the right surface, even though other cell types (eg, vascular
smooth muscle cells, mesothelial cells) and certain antithrombotic
proteins might be able to form a suitable covering.2 3 4 If
the endothelium is the right surface, then certain
assumptions must be made. First, endothelium can be
seeded onto the graft or induced to grow from local sources to form a
confluent layer at the surface. Second, the endothelium
over a graft behaves like endothelium over a normal
artery
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