Department of Life Sciences, National Central University, Jhongli 32001, Taiwan.
Department of Chemistry, National Central University, Jhongli 32001, Taiwan.
Mol Cell Endocrinol. 2014 Mar 5;383(1-2):147-58. doi: 10.1016/j.mce.2013.12.008. Epub 2013 Dec 19.
Valproic acid (VPA) has been shown to increase the reprogramming efficiency of induced pluripotent stem cells (iPSC) from somatic cells, but the mechanism by which VPA enhances iPSC induction has not been defined. Here we demonstrated that VPA directly activated Oct4 promoter activity through activation of the PI3K/Akt/mTOR signaling pathway that targeted the proximal hormone response element (HRE, -41∼-22) in this promoter. The activating effect of VPA is highly specific as similar compounds or constitutional isomers failed to instigate Oct4 promoter activity. We further demonstrated that the upstream 2 half-sites in this HRE were essential to the activating effect of VPA and they were targeted by a subset of nuclear receptors, such as COUP-TFII and TR2. These findings show the first time that NRs are implicated in the VPA stimulated expression of stem cell-specific factors and should invite more investigation on the cooperation between VPA and NRs on iPSC induction.
丙戊酸(VPA)已被证明能提高体细胞诱导多能干细胞(iPSC)的重编程效率,但 VPA 增强 iPSC 诱导的机制尚未确定。在这里,我们证明 VPA 通过激活 PI3K/Akt/mTOR 信号通路直接激活 Oct4 启动子活性,该通路靶向该启动子中的近端激素反应元件(HRE,-41∼-22)。VPA 的激活作用具有高度特异性,因为类似的化合物或立体异构体不能引发 Oct4 启动子活性。我们进一步证明,该 HRE 中的上游 2 个半位点对于 VPA 的激活作用至关重要,它们被一些核受体靶向,如 COUP-TFII 和 TR2。这些发现首次表明 NRs 参与了 VPA 刺激的干细胞特异性因子的表达,这应该会促使更多关于 VPA 和 NRs 在 iPSC 诱导方面的合作的研究。