Journal
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Volume 29, Issue 2, Pages 246-253Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/ATVBAHA.108.179218
Keywords
heart valves; valvular interstitial cells; simvastatin; calcification; extracellular matrix
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Funding
- National Science Foundation CAREER Award [CBET-0547374]
- National Institutes of Health Translational Cardiovascular Sciences Traineeship [T32-HL 007936-06]
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Objective-The lack of therapies that inhibit valvular calcification and the conflicting outcomes of clinical studies regarding the impact of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors on valve disease highlight the need for controlled investigations to characterize the interactions between HMG-CoA reductase inhibitors and valve tissue. Thus, we applied multiple in vitro disease stimuli to valvular interstitial cell (VIC) cultures and examined the impact of simvastatin treatment on VIC function. Methods and Results-VICs were cultured on 3 different substrates that supported various levels of nodule formation. Transforming growth factor (TGF)-beta 1 was also applied as a disease stimulus to VICs on 2-D surfaces or encapsulated in 3-D collagen gels and combined with different temporal applications of simvastatin. Simvastatin inhibited calcific nodule formation in a dose-dependent manner on all materials, although the level of statin efficacy was highly substrate-dependent. Simvastatin treatment significantly altered nodule morphology, resulting in dramatic nodule dissipation over time, also in a substrate-dependent manner. These effects were mimicked in 3-D cultures, wherein simvastatin reversed TGF-beta 1-induced contraction. Decreases in nodule formation were not achieved via the HMG-CoA reductase pathway, but were correlated with decreases in ROCK activity. Conclusions-These studies represent a significant contribution to understanding how simvastatin may impact heart valve calcification. (Arterioscler Thromb Vasc Biol. 2009; 29: 246-253.)
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