We characterized human umbilical vein (HUV) endothelial cells as to cell growth and prostacyclin production to get a better understanding of the properties of endothelial cells. Endothelial cell growth supplement (ECGS) and basic fibroblast growth factor (FGF) stimulated HUV endothelial cell growth.
4-Hydroxynonenal induces membrane perturbations and inhibition of basal prostacyclin production in endothelial cells, and migration of monocytes.
✍ Scribed by Nicanor I. Moldovan; Florea Lupu; Leni Moldovan; Nicolae Simionescu
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 655 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1065-6995
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✦ Synopsis
ABSTRACT
Cultured bovine aortic endothelial cells (BAEC) were incubated for 5 days with 10^−5^ 4‐hydroxynonenal (HN). HN treated BAEC and controls were either (i) further incubated with ^125^I‐polymyxin B (IPxB) or with radioiodinated, inactivated coagulation factor Xa (IFXai) as markers of membrane phospholipid perturbation, or (ii) assayed for the synthesis of prostacyclin (PGI~2~) and thromboxane A~2~ (TXA~2~). Rabbit blood mononuclear cells enriched in monocytes (MC) were isolated and assayed for chemotactic response to HN. The results showed six ‐ fold increases of IPxB and IFXai binding to BAEC treated with HN, as compared to untreated controls. We also found in HN treated cells a marked inhibition of PGI~2~ synthesis, but an unmodified TXA~2~ production. In addition, HN in the 10‐5‐10‐10 M range induced oriented migration of MC.
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