Thromb Haemost 2008; 100(03): 489-497
DOI: 10.1160/TH07-12-0760
Endothelium and Vascular Development
Schattauer GmbH

Simvastatin-induced endothelial cell detachment and microparticle release are prenylation dependent

Michaela Diamant
1   Department of Endocrinology / Diabetes Center, VU University Medical Center, Amsterdam, The Netherlands
,
Maarten E. Tushuizen
1   Department of Endocrinology / Diabetes Center, VU University Medical Center, Amsterdam, The Netherlands
,
Mohammed N. Abid-Hussein
2   Department of Clinical Chemistry, Academic Medical Center, Amsterdam, The Netherlands
,
Chi M. Hau
2   Department of Clinical Chemistry, Academic Medical Center, Amsterdam, The Netherlands
,
Anita N. Böing
2   Department of Clinical Chemistry, Academic Medical Center, Amsterdam, The Netherlands
,
Augueste Sturk
2   Department of Clinical Chemistry, Academic Medical Center, Amsterdam, The Netherlands
,
Rienk Nieuwland
2   Department of Clinical Chemistry, Academic Medical Center, Amsterdam, The Netherlands
› Author Affiliations
Further Information

Publication History

Received 31 December 2007

Accepted after major revision 24 June 2008

Publication Date:
22 November 2017 (online)

Summary

Statins reduce cardiovascular disease risk and affect endothelial function by cholesterol-dependent and independent mechanisms. Recently, circulating (detached) endothelial cells and endothelial microparticles (EMP) have been associated with endothelial functioning in vitro and in vivo.We investigated whether simvastatin affects endothelial detachment and release of EMP. Human umbilical vein endothelial cells (HUVECs) were incubated with clinically relevant concentrations of simvastatin (1.0 and 5.0 µM), with or without mevalonic acid (100 µM) or gera-nylgeranylpyrophosphate (GGPP; 20 µM) for 24 hours, and analyzed by flowcytometry andWe stern blot. Simvastatin at 1.0 and 5.0 µM increased cell detachment from 12.5 ± 4.1% to 26.0 ± 7.6% (p=0.013) and 28.9 ± 2.2% (p=0.002) as well as EMP release (p=0.098 and p=0.041, respectively).The majority of detached cells was apoptotic, although the fraction of detached cells that showed signs of apoptosis (>70%) was unaffected by simvastatin. Detached cells and EMP contained caspase 3 and caspase 8,but not caspase 9. Restoring either cholesterol biosynthesis and prenylation (mevalonate) or prenylation alone (GGPP) reversed all simvastatin-induced effects on cell detachment and EMP release. Adherent cells showed no signs of simvastatin-induced apoptosis. Simvastatin promotes detachment and EMP release by inhibiting prenylation, presumably via a caspase 8-dependent mechanism. We hypothesize that by facilitating detachment and EMP release, statins improve the overall condition of the remaining vascular endothelium.

 
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