Author/Authors :
Samson، نويسنده , , Karen Thursday R. and Minoguchi، نويسنده , , Kenji F. Tanaka، نويسنده , , Akihiko and Oda، نويسنده , , Naruhito and Yokoe، نويسنده , , Takuya and Okada، نويسنده , , Shinji and Yamamoto، نويسنده , , Yoshitaka and Watanabe، نويسنده , , Yoshio and Yamamoto، نويسنده , , Mayumi and Ohta، نويسنده , , Shin-ichi Adachi، نويسنده , , Mitsuru، نويسنده ,
Abstract :
Statins are lipid-lowering agents with pleiotropic effects. We investigated the apoptotic effects of fluvastatin on peripheral CD4+ T cells from healthy subjects. Fluvastatin induced apoptosis in resting CD4+ T cells but not in CD4+ T cells strongly activated with a high concentration of PMA plus ionomycin (PMA/I) analyzed with annexin V and propidium iodide staining. However, CD4+ T cells activated with a low concentration of PMA/I or with anti-CD3 antibodies were apoptotic after treatment with fluvastatin. Activities of caspases-8, -9, and -3 were increased in resting CD4+ T cells treated with fluvastatin (10 μM). In strongly activated CD4+ T cells, fluvastatin inhibited the activation of caspase-8 induced by PMA/I and increased caspase-9 activity. The caspase-3 activity did not differ between untreated and fluvastatin-treated strongly activated CD4+ T cells. Treatment with fluvastatin (10 μM) enhanced cytochrome c release and increased the Bax/Bcl-2 ratio in both resting and strongly activated CD4+ T cells. Although the in vitro concentration of fluvastatin used in this study is higher than in vivo, other factors may sensitize apoptotic cell death of CD4+ T cells in vivo. In conclusion, fluvastatin induces apoptosis in resting T cells but not in strongly activated T cells, a difference that might be due to the interaction between caspase-8 and caspase-9.
Keywords :
statin , T cells , apoptosis , Cell Proliferation