Atorvastatin attenuates TLR4-mediated NF-κB activation in a MyD88-dependent pathway.
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2009-03
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Abstract
Antigen presenting cells such as dendritic cells and macrophages have recently been detected in atherosclerotic plaques. Toll-like receptors expressed on the surface of these cells, have been implicated in ongo-ing inflammatory responses in the plaques. In this study, we investigated the anti-inflammatory effect of atorvas-tatin, a lipid lowering drug, via Toll-like receptor 4 (TLR4) in vitro, employing murine pro-B cell lines transfected with hTLR4/MD2 and MyD88/hTLR4/MD2 systems. The results showed that atorvastatin at 10 μM significantly attenu-ated NF-κB activation within 24 hours while at lower doses of 0.1 and 1 μM, treatment time had to be prolonged up to 48 hours for a significant inhibition to occur. The inhibition of NF-κB was also observed in a cell line co-transfected with MyD88 and TLR4 suggesting that the attenuation of NF-κB by atorvastatin occurred in a MyD88 dependent fashion.
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Chansrichavala Praveen, Chantharaksri Udom, Sritara Piyamitr, Chaiyaroj Sansanee C. Atorvastatin attenuates TLR4-mediated NF-κB activation in a MyD88-dependent pathway. Asian Pacific Journal of Allergy and Immunology, 2009 Mar; 27(1): 49-57.