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Sphingosine kinase 1 overexpression stimulates intestinal epithelial cell proliferation through increased c-Myc translation

机译:鞘氨醇激酶1过表达通过增加c-Myc翻译刺激肠上皮细胞增殖

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摘要

Sphingosine-1-phosphate (S1P), through mechanisms that are not completely understood, is shown to modulate cellular proliferation, which is critically important for maintaining the integrity of intestinal epithelium. Here, we show that increased S1P promotes proliferation in intestinal epithelial cells. We found that overexpression of sphingosine kinase 1 (SphK1), the rate-limiting enzyme for S1P synthesis, significantly increased cell proliferation and that this occurred through enhanced expression of c-Myc. Further, we found that the increased pattern of expression of c-Myc occurred predominantly due to its increased translation. The overexpressed SphK1 led to increased checkpoint kinase 2 and enhanced HuR phosphorylation which allowed for increased translation of c-Myc mRNA through HuR binding at the 3′-untranslated regions. Our findings demonstrate that S1P modulates intestinal cell proliferation and provides new insights as to the mechanistic actions of SphK1 and S1P in maintaining intestinal epithelial homeostasis.
机译:鞘氨醇-1-磷酸(S1P)通过尚未完全了解的机制可调节细胞增殖,这对于维持肠上皮的完整性至关重要。在这里,我们表明增加的S1P促进肠上皮细胞增殖。我们发现鞘氨醇激酶1(SphK1),S1P合成的限速酶的过表达,显着增加了细胞增殖,并且这是通过增强c-Myc的表达而发生的。此外,我们发现c-Myc表达模式的增加主要是由于c-Myc翻译的增加。过表达的SphK1导致增加的检查点激酶2和增强的HuR磷酸化,从而允许通过3'非翻译区的HuR结合增加c-Myc mRNA的翻译。我们的发现表明,S1P调节肠道细胞的增殖,并为SphK1和S1P在维持肠道上皮稳态中的机制作用提供了新的见解。

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