首页> 外文期刊>The biochemical journal >Green tea polyphenol EGCG induces lipid-raft clustering and apoptotic cell death by activating protein kinase Cδ and acid sphingomyelinase through a 67 kDa laminin receptor in multiple myeloma cells
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Green tea polyphenol EGCG induces lipid-raft clustering and apoptotic cell death by activating protein kinase Cδ and acid sphingomyelinase through a 67 kDa laminin receptor in multiple myeloma cells

机译:绿茶多酚EGCG通过67 kDa层粘连蛋白受体激活多发性骨髓瘤细胞中的蛋白激酶Cδ和酸性鞘磷脂酶来诱导脂质筏聚集和凋亡细胞死亡。

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pEGCG [(?)-epigallocatechin-3-iO/i-gallate], the major polyphenol of green tea, has cancer chemopreventive and chemotherapeutic activities. EGCG selectively inhibits cell growth and induces apoptosis in cancer cells without adversely affecting normal cells; however, the underlying molecular mechanism iin vivo/i is unclear. In the present study, we show that EGCG-induced apoptotic activity is attributed to a lipid-raft clustering mediated through 67LR (67 kDa laminin receptor) that is significantly elevated in MM (multiple myeloma) cells relative to normal peripheral blood mononuclear cells, and that aSMase (acid sphingomyelinase) is critical for the lipid-raft clustering and the apoptotic cell death induced by EGCG. We also found that EGCG induces aSMase translocation to the plasma membrane and PKCδ (protein kinase Cδ) phosphorylation at Sersup664/sup, which was necessary for aSMase/ceramide signalling via 67LR. Additionally, orally administered EGCG activated PKCδ and aSMase in a murine MM xenograft model. These results elucidate a novel cell-death pathway triggered by EGCG for the specific killing of MM cells./p
机译:绿茶的主要多酚> EGCG [(?)-epigallocatechin-3- O -没食子酸盐]具有化学预防和化学治疗作用。 EGCG选择性抑制癌细胞生长并诱导癌细胞凋亡,而不会对正常细胞产生不利影响;然而,体内的潜在分子机制尚不清楚。在本研究中,我们表明EGCG诱导的细胞凋亡活性归因于通过67LR(67kDa层粘连蛋白受体)介导的脂筏聚类,相对于正常外周血单核细胞,MM(多发性骨髓瘤)细胞中脂聚簇明显升高,而且aSMase(酸性鞘磷脂酶)对于脂筏聚集和EGCG诱导的凋亡细胞死亡至关重要。我们还发现,EGCG诱导aSMase易位至质膜和PKCδ(蛋白激酶Cδ)在Ser 664 磷酸化,这对于通过67LR进行aSMase /神经酰胺信号传递是必需的。另外,在鼠MM异种移植模型中,口服给予EGCG激活了PKCδ和aSMase。这些结果阐明了EGCG触发的一种新的细胞死亡途径,可以特异性杀伤MM细胞。

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