TY - JOUR
T1 - Calcium Phosphate Crystals Induce Cell Death in Human Vascular Smooth Muscle Cells
T2 - A Potential Mechanism in Atherosclerotic Plaque Destabilization
AU - Ewence, Alexandra E.
AU - Bootman, Martin
AU - Roderick, H. Llewelyn
AU - Skepper, Jeremy N.
AU - McCarthy, Geraldine
AU - Epple, Matthias
AU - Neumann, Markus
AU - Shanahan, Catherine M.
AU - Proudfoot, Diane
PY - 2008/8/29
Y1 - 2008/8/29
N2 - Vascular calcification is associated with an increased risk of myocardial infarction; however, the mechanisms linking these 2 processes are unknown. Studies in macrophages have suggested that calcium phosphate crystals induce the release of proinflammatory cytokines; however, no studies have been performed on the effects of calcium phosphate crystals on vascular smooth muscle cell function. In the present study, we found that calcium phosphate crystals induced cell death in human aortic vascular smooth muscle cells with their potency depending on their size and composition. Calcium phosphate crystals of approximately 1 mu m or less in diameter caused rapid rises in intracellular calcium concentration, an effect that was inhibited by the lysosomal proton pump inhibitor, bafilomycin A1. Bafilomycin A1 also blocked vascular smooth muscle cell death suggesting that crystal dissolution in lysosomes leads to an increase in intracellular calcium levels and subsequent cell death. These studies give novel insights into the bioactivity of calcified deposits and suggest that small calcium phosphate crystals could destabilize atherosclerotic plaques by initiating inflammation and by causing vascular smooth muscle cell death. (Circ Res. 2008; 103: e28-e34.)
AB - Vascular calcification is associated with an increased risk of myocardial infarction; however, the mechanisms linking these 2 processes are unknown. Studies in macrophages have suggested that calcium phosphate crystals induce the release of proinflammatory cytokines; however, no studies have been performed on the effects of calcium phosphate crystals on vascular smooth muscle cell function. In the present study, we found that calcium phosphate crystals induced cell death in human aortic vascular smooth muscle cells with their potency depending on their size and composition. Calcium phosphate crystals of approximately 1 mu m or less in diameter caused rapid rises in intracellular calcium concentration, an effect that was inhibited by the lysosomal proton pump inhibitor, bafilomycin A1. Bafilomycin A1 also blocked vascular smooth muscle cell death suggesting that crystal dissolution in lysosomes leads to an increase in intracellular calcium levels and subsequent cell death. These studies give novel insights into the bioactivity of calcified deposits and suggest that small calcium phosphate crystals could destabilize atherosclerotic plaques by initiating inflammation and by causing vascular smooth muscle cell death. (Circ Res. 2008; 103: e28-e34.)
U2 - 10.1161/CIRCRESAHA.108.181305
DO - 10.1161/CIRCRESAHA.108.181305
M3 - Article
VL - 103
SP - E28 - E34
JO - Circulation Research
JF - Circulation Research
IS - 5
ER -