Sphingosine arrests the cell cycle and induces apoptosis by targeting sphingosine-dependent protein kinase and protein kinase Cδ in vitro

Takeshi Kanno , Akinobu Gotoh , Tomoyuki Nishizaki
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引用次数: 4

Abstract

Purpose

Emerging evidence has indicated that the sphingolipid sphingosine is involved in cellular differentiation, cell growth, and apoptosis. Here, we elucidated the sphingosine signaling pathways underlying apoptosis and cell growth inhibition.

Study section and results

Sphingosine induced mitochondria-mediated apoptosis in rat hippocampal neurons and astrocytes by activating caspase-3/-9 via the sphingosine-dependent protein kinase (SDK)/14-3-3 protein/Bax/cytochrome c pathway. This may account for the implication of sphingosine/SDK in the pathogenesis of Alzheimer's disease. Additionally, sphingosine induced apoptosis in MKN-28 human gastric cancer cells in an SDK-dependent manner. In the human malignant pleural mesothelioma cell lines, sphingosine suppressed cell growth by arresting the cell cycle at the G0/G1 phase, along with inhibiting protein kinase Cδ (PKCδ). This suggests that sphingosine/SDK/PKCδ signaling can be potentially used in treating many types of cancers.

Conclusion

The present review shows that sphingosine induces apoptosis and inhibits the cell cycle by targeting SDK and PKCδ. Our findings represent a fresh insight into sphingosine signaling pathways, and may provide a blueprint for developing drugs for treating Alzheimer's disease and many types of cancers.

鞘氨醇通过体外靶向鞘氨醇依赖蛋白激酶和蛋白激酶Cδ抑制细胞周期,诱导细胞凋亡
目的越来越多的证据表明鞘脂鞘肽参与细胞分化、生长和凋亡。在这里,我们阐明了鞘氨醇信号通路在细胞凋亡和细胞生长抑制中的作用。研究部分和结果鞘氨醇通过鞘氨醇依赖性蛋白激酶(SDK)/14-3-3蛋白/Bax/细胞色素c通路激活caspase-3/-9,诱导线粒体介导的大鼠海马神经元和星形胶质细胞凋亡。这可能解释了鞘氨醇/SDK在阿尔茨海默病发病机制中的作用。此外,鞘氨醇以sdk依赖的方式诱导MKN-28人胃癌细胞凋亡。在人恶性胸膜间皮瘤细胞系中,鞘氨醇通过抑制蛋白激酶Cδ (PKCδ)抑制G0/G1期的细胞周期来抑制细胞生长。这表明鞘氨醇/SDK/PKCδ信号可以潜在地用于治疗多种类型的癌症。结论鞘氨醇通过靶向SDK和PKCδ诱导细胞凋亡,抑制细胞周期。我们的发现代表了对鞘氨醇信号通路的新见解,并可能为开发治疗阿尔茨海默病和许多类型癌症的药物提供蓝图。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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