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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
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.
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