Low density lipoprotein (LDL) oxidation is characterized by alterations in
biological properties and structure of the lipoprotein particles, including
breakdown and modification of apolipoprotein B (apoB). We compared apoB br
eakdown patterns in different models of minimally and extensively oxidized
LDL using Western blotting techniques and several monoclonal and polyclonal
antibodies. It was found that copper and endothelial cell-mediated oxidati
on produced a relatively similar apoB banding pattern with progressive frag
mentation of apoB during LDL oxidation, whereas malondialdehyde (MDA)- and
hydroxynonenal (HNE)-modified LDL produced an aggregated apoB. It is concei
vable that apoB fragments present in copper and endothelial cell oxidized L
DL lead to the exposure on the lipoprotein surface of different protein epi
topes than in aggregated MDA-LDL and HNE-LDL. Although all models of extens
ively oxidized LDL led to increased lipid uptake in macrophages, mild degre
es of oxidation interfered with LDL uptake in fibroblasts and extensively o
xidized LDL impaired degradation of native LDL in fibroblasts. We suggest t
hat in order to improve interpretation and comparison of results, data obta
ined with various models of oxidized LDL should be compared to the simplies
t and most reproducible models of 3 h and 18 h copper-oxidized LDL (apoB br
eakdown) and MDA-LDL (apoB aggregation) since different models of oxidized
LDL have significant differences in apoB breakdown and aggregation patterns
which may affect immunological and biological properties of oxidized LDL.