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Updated: Aug 10, 2026

Quantitation of Endothelial Cell Adhesiveness In Vitro
Published on: June 18, 2015
Endothelial cell-derived foam cells fail to express adhesion molecules (ICAM-1 and VCAM-1) for monocytes
E Constantinescu1, D Alexandru, V Alexandru
1Institute of Cellular Biology and Pathology N. Simionescu, Bucharest, Romania. econstantinescu@simionescu.instcellbiopath.ro
Insights
Endothelial cell-derived foam cells, crucial in advanced atherosclerosis, do not express ICAM-1 or VCAM-1, significantly reducing monocyte adhesion. This finding offers a new model for studying atherosclerosis progression.
Area of Science:
- Cell Biology
- Immunology
- Cardiovascular Research
Background:
- Atherosclerosis involves endothelial dysfunction and lipid accumulation.
- Cell adhesion molecules like ICAM-1 and VCAM-1 play roles in early atherosclerotic lesion development.
- Endothelial cell-derived foam cells are characteristic of advanced atherosclerotic plaques.
Purpose of the Study:
- To investigate the expression of ICAM-1 and VCAM-1 in cultured endothelial cell-derived foam cells.
- To evaluate the adhesion properties of these foam cells for monocytes.
Main Methods:
- Hamster aortic endothelial cells (HAEC) were cultured and exposed to hypercholesterolemic or normal serum.
- Foam cell formation was induced by hypercholesterolemic serum.
- Indirect immunofluorescence was used to assess ICAM-1 and VCAM-1 expression.
- Monocyte adhesion assays were performed using freshly isolated hamster monocytes.
Main Results:
- HAEC exposed to hypercholesterolemic serum formed foam cells with numerous lipid droplets.
- Normal HAEC expressed low levels of ICAM-1 and VCAM-1.
- HAEC-derived foam cells showed no detectable expression of ICAM-1 and VCAM-1.
- Monocyte adhesion to HAEC-derived foam cells was significantly reduced compared to normal HAEC.
Conclusions:
- Endothelial cell-derived foam cells lack surface expression of ICAM-1 and VCAM-1.
- These foam cells exhibit minimal to no adhesion capacity for monocytes.
- This experimental model provides insights into cellular changes in advanced atherosclerosis stages.
Abstract:
The purpose of this study was to assess the expression of cell adhesion molecules ICAM-1 (intercellular adhesion molecule-1) and VCAM-1 (vascular cell adhesion molecule-1) in endothelial cell-derived foam cells. Hamster aortic endothelial cells (HAEC) in culture were exposed to hypercholesterolemic or normal homologous serum for 24 h. At the end of the incubation period, HAEC exposed to hypercholesterolemic serum exhibited numerous lipid droplets and had a general aspect of foam cells. When examined for the expression of ICAM-1 and VCAM-1 (by indirect immunofluorescence) normal HAEC expressed constitutively (to low level) on their surface these adhesion molecules; however HAEC-derived foam cells failed to display any labeling. To further assess these results, HAEC were first incubated with normal or hypercholesterolemic sera (as above) and then exposed to freshly isolated normal hamster blood monocytes. These experiments showed that monocytes adhered in small number to normal cells and failed to adhere to the surface of HAEC-derived foam cells. Together these data indicate that endothelial cell-derived foam cells: a) do not express ICAM-1 and VCAM-1 on their surface; b) have low or no adhesion properties for monocytes and c) may represent an appropriate experimental model to study the cellular alterations that take place in the advanced stages of atherosclerosis.
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