蛋白激酶Cα亚型调控胶质瘤细胞MAP激酶ERK1/2的激活:参与细胞存活和基因表达

Marianne Leirdal, Mouldy Sioud
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引用次数: 15

摘要

蛋白激酶C是一个丝氨酸/苏氨酸蛋白激酶家族,参与许多细胞反应,包括细胞存活和凋亡。我们最近发现,核酸酶特异性抑制PKCα异构体可诱导敏感细胞凋亡。我们发现,在PKCα DNA酶处理的胶质瘤细胞中,MAP激酶ERK1/2的激活被抑制,而它们的总水平没有受到治疗的显著影响。当PKC的特异性抑制剂calphostin抑制PKC的整体活性时,也得到了类似的结果。这些结果表明ERK1/2信号通路在胶质瘤细胞存活中起重要作用,PKCα亚型是该通路的主要调节剂。此外,我们发现ERK1/2信号通路是碱性成纤维细胞生长因子的组成性表达所必需的,碱性成纤维细胞生长因子是胶质瘤细胞生长的一种有效的有丝分裂原。
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Protein Kinase Cα Isoform Regulates the Activation of the MAP Kinase ERK1/2 in Human Glioma Cells: Involvement in Cell Survival and Gene Expression

Protein kinase C is a family of serine/threonine protein kinases involved in many cellular responses, including cell survival and apoptosis. We have recently found that specific inhibition of the PKCα isoform by nucleic acid enzymes induced apoptosis in sensitive cells. Here we show that in PKCα DNA enzyme-treated glioma cells the activation of MAP kinases ERK1/2 is inhibited, whereas their total level was not significantly affected by the treatment. Similar results were obtained when the overall activity of the PKC was inhibited by calphostin, a specific inhibitor for PKC. These results would indicate that the ERK1/2 signaling pathway plays an important role in glioma cell survival and that the PKCα isoform is the main modulator of this pathway. Furthermore, we show that the ERK1/2 signaling pathway is required for the constitutive expression of the basic fibroblast growth factor, a potent mitogen for glioma cell growth.

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