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[摘要]：We have demonstrated that protein kinase C delta (PKC delta) could be involved in macrophage apoptosis induced by cationic liposomes composed of stearylamine (SA-liposomes), but the detailed mechanism of how SA-liposomes activate PKC delta has remained unclear. In this paper, we clarified whether lipid rafts are involved in the PKC delta activation induced by SA-liposomes. Co-localization of SA-liposomes and Cholera toxin B subunit (CBT), which specifically binds to ganglioside GM1 on lipid rafts, was found by microscopic observation. The incorporation of SA-liposomes into lipid rafts was clearly inhibited by the pretreatment of cells with an agent, 2,6-di-O-methyl-alpha-cyclodextrin (DM-alpha-CD) which disrupts lipid rafts. Activation of PKC delta and externalization of phosphatidylserine induced by SA-liposomes were also suppressed by DM-alpha-CD, which extracts sphingolipids and proteins from lipid rafts. Reactive oxygen species (ROS) generation, which could be involved in the macrophage apoptosis, was also inhibited by DM-alpha-CD. Furthermore, apoptosis induced by SA-liposomes was clearly inhibited when the cells were pre-treated with DM-alpha-CD, but but not nystatin, a cholesterol-sequestering agent that disrupt lipid rafts. These findings suggest that sphingolipids in lipid rafts are involved in the activation of PKC delta which leads to apoptosis induced by cationic liposomes, SA-liposomes. (C) 2011 Elsevier Inc. All rights reserved. |
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