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Perillyl Alcohol, an Inhibitor of Geranylgeranyl Transferase, Induces Apoptosis of Immortalized Human Vascular Smooth Muscle Cells In Vitro
- Source :
- Journal of Cardiovascular Pharmacology. 35:341-344
- Publication Year :
- 2000
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 2000.
-
Abstract
- The isoprenoids geranylgeraniol and farnesol are required for lipid modification of several important cellular proteins. In this study the effect of perillyl alcohol (PA), an inhibitor of geranylgeranyl transferase, was examined on proliferation and apoptosis of immortalized human vascular smooth muscle cells (HVSMCs) derived from saphenous vein. PA induced a time- and concentration-dependent inhibition of cell proliferation over 3 days and 48 h exposure to PA inhibited [methyl-3H-thymidine incorporation induced by 10% fetal calf serum in a concentration-dependent manner. Flow cytometry analysis indicated that PA reduced the proportion of cells in S phase and increased apoptosis. PA-induced apoptosis was confirmed by terminal deoxynucleotidyl transferase (TdT) reagent-based immunocytochemistry. In contrast, the selective inhibitors of farnesyl transferase B581 and BZA-5B were without effect. In view of the proposed role of proliferation and apoptosis in myointimal hyperplasia, inhibitors of geranylgeranyl transferases may have therapeutic potential in cardiovascular disease.
- Subjects :
- Geranylgeranyl Transferase
Programmed cell death
Time Factors
Vascular smooth muscle
Apoptosis
In Vitro Techniques
Biology
Muscle, Smooth, Vascular
Benzodiazepines
chemistry.chemical_compound
Geranylgeraniol
DNA Nucleotidylexotransferase
Humans
Saphenous Vein
Enzyme Inhibitors
Pharmacology
Alkyl and Aryl Transferases
Dose-Response Relationship, Drug
Terpenes
Immunochemistry
Perillyl alcohol
Flow Cytometry
Molecular biology
Terminal deoxynucleotidyl transferase
Biochemistry
chemistry
Monoterpenes
Lipid modification
Cardiology and Cardiovascular Medicine
Oligopeptides
Cell Division
Thymidine
Subjects
Details
- ISSN :
- 01602446
- Volume :
- 35
- Database :
- OpenAIRE
- Journal :
- Journal of Cardiovascular Pharmacology
- Accession number :
- edsair.doi.dedup.....4c46b1542c4a50c0a8552077f671694b