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1 Cardiovascular Research Unit, Center for Molecular Medicine L8:03, Karolinska Institute, S-17176 Stockholm, Sweden; and 2 Institut für Prophylaxe der Kreislaufkrankheiten, D-80336 Munich, Germany
Pyrrolidine dithiocarbamate (PDTC) has been found to
induce or inhibit apoptosis in different cell types. Here we show that PDTC dose-dependently reduced the viability of rat smooth muscle cells
(rSMC), human fibroblasts, and endothelial cells at low but not at high
cell density. Endothelial cells were least sensitive, fibroblasts
showed a medium sensitivity, and rSMC showed a high sensitivity to
PDTC-mediated cell death. An early reduction in the mitochondrial
membrane potential indicated a rapid onset of apoptosis in rSMC.
Apoptosis was further confirmed by annexin V staining and DNA
fragmentation analysis. Gel shift analysis demonstrated increased
nuclear factor (NF)-
B activity in high-density rSMC compared with
low-density cells. NF-
B has recently been shown to regulate the
induction of anti-apoptotic proteins. Although PDTC is widely used as
an inhibitor for NF-
B and a radical scavenger, our data show that
PDTC rather enhanced NF-
B activity and, alone or in combination with
menadione, induced oxygen radical generation. Notably, PDTC failed to
reduce rSMC viability in medium without Cu2+ or
Zn2+, and addition of Cu2+ or Zn2+
resulted in a dose-dependent increase in PDTC-induced cell death. Addition of both Cu2+ and Zn2+ showed
synergistic effects. Our results indicate that the induction of
apoptosis by PDTC requires Cu2+ and Zn2+ and is
dependent on cell type and density. Such differential effects may have
implications for studies of PDTC as an anti-atherosclerotic or
immunomodulatory drug.
cell density; smooth muscle cells; copper ion; zinc ion
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