Berthier A, Lemaire-Ewing S, Prunet C, Monier S, Athias A, Bessède G, Pais de Barros J-P, Laubriet A, Gambert P, Lizard G, Néel D
Inserm U498 Métabolisme des lipoprotéines humaines et interactions vasculaires/IFR 100 Inserm, CHU/Hôpital du Bocage, BP77908, 21079 Dijon Cedex, France.
Cell Death Differ. 2004 Aug;11(8):897-905. doi: 10.1038/sj.cdd.4401434.
7-Ketocholesterol is a component of oxidized LDL, which plays a central role in atherosclerosis. It is a potent inducer of cell death towards a wide number of cells involved in atherosclerosis. In this study, it is reported that 7-ketocholesterol treatment induces an increase of cytosolic-free Ca(2+) in THP-1 monocytic cells. This increase is correlated with the induction of cytotoxicity as suggested from experiments using the Ca(2+) channel blockers verapamil and nifedipine. This 7-ketocholesterol-induced apoptosis appears to be associated with the dephosphorylation of serine 75 and serine 99 of the proapoptotic protein Bcl-2 antagonist of cell death (BAD). We demonstrated that this dephosphorylation results mainly from the activation of calcium-dependent phosphatase calcineurin by the oxysterol-induced increase in Ca(2+). Moreover, this Ca(2+) increase appears related to the incorporation of 7-ketocholesterol into lipid raft domains of the plasma membrane, followed by the translocation of transient receptor potential calcium channel 1, a component of the store operated Ca(2+) entry channel, to rafts.
7-酮胆固醇是氧化型低密度脂蛋白的一个组成部分,在动脉粥样硬化中起核心作用。它是多种参与动脉粥样硬化的细胞发生细胞死亡的强效诱导剂。在本研究中,据报道7-酮胆固醇处理可诱导THP-1单核细胞胞质游离Ca(2+)增加。如使用Ca(2+)通道阻滞剂维拉帕米和硝苯地平所做实验表明,这种增加与细胞毒性的诱导相关。这种7-酮胆固醇诱导的细胞凋亡似乎与促凋亡蛋白细胞死亡的Bcl-2拮抗剂(BAD)的丝氨酸75和丝氨酸99去磷酸化有关。我们证明这种去磷酸化主要是由氧甾醇诱导的Ca(2+)增加激活钙依赖性磷酸酶钙调神经磷酸酶所致。此外,这种Ca(2+)增加似乎与7-酮胆固醇掺入质膜的脂筏结构域有关,随后瞬时受体电位钙通道1(储存操纵性Ca(2+)进入通道的一个组成部分)转位至脂筏。