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From the Institut für Arterioskleroseforschung (P.C., S.M., B.B., A.C., G.A.), Institut für Allgemeine Zoologie und Genetik (S.M.), and Institut für Klinische Chemie und Laboratoriumsmedizin (G.A.), Westfälische Wilhelms-Universität Münster, Münster, Germany.
Correspondence to Dr Paul Cullen, Institut für Arterioskleroseforschung, Domagkstraße 3, 48149 Münster, Germany. E-mail cullen{at}uni-muenster.de.
Abstract Identification of genes expressed during foam cell
formation is important for understanding the molecular basis of
atherosclerosis. We used polymerase chain reaction
(PCR)based differential display to isolate differentially expressed
cDNA species in foam cells induced by incubation of human
monocyte-derived macrophages in the presence of
acetylated or oxidized LDL. This led to identification of a
306-bp cDNA with 100% homology to type IV fucosyltransferase
(Fuc-TIV), which was downregulated by factors of 20 and 3 in
acetylated LDL and oxidized LDLloaded macrophages,
respectively. This enzyme is sufficient for the expression of Lewis X
and sialyl Lewis X, carbohydrate adhesion molecules that bind to
receptors of the selectin family. Expression of a second
fucosyltransferase (Fuc-TVII) that synthesizes sialyl Lewis X but not
Lewis X was shown by quantitative reverse transcriptionPCR to also be
reduced, by 40% and 20% in acetylated LDL and oxidized
LDLloaded macrophages, respectively.
-(1,3)-Fucosyltransferase enzyme activity was reduced in lysates
from both acetylated LDL and oxidized LDLloaded cells.
Analysis by flow cytometry showed reduced expression of the
CD15 (corresponding to Lewis X) and CD15s (sialyl Lewis X) antigens on
the surface of cells loaded with either acetylated or oxidized
LDL. Transformation of macrophages into foam cells results in
reduced expression of selectin-binding ligands on the surface of such
cells.
Key Words: atherosclerosis monocyte-derived macrophages foam cells differential display fucosyltransferase IV
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