Institute of Biochemistry and Biophysics, University of Tehran, P.O. Box 13145-1384, Tehran, Iran.
Cell Biochem Biophys. 2013 Nov;67(2):675-87. doi: 10.1007/s12013-013-9557-0.
It is well established that Foxo3a is a fundamental module of signal transduction pathways regulating erythropoiesis; however, precise mechanism which regulates its physiological function still remains unclear. Here, our results revealed that the nuclear localization and stability of Foxo3a were modulated by the physical interaction of PKC and p38 signaling elements and that direct interactions led to phosphorylation of threonine residue(s) in Foxo3a. In addition, our findings revealed that the sequential activity of Foxo3a by guanosine 5'-triphosphate can impede cellular proliferation and suppress p73 expression as oncoprotein in K562 cells; thus identifying Foxo3a as a tumor suppressor in these p53 null cells. However, down-regulation of Foxo3a-dependent p73 expression causes cell differentiation along the erythroid lineage. Collectively, our findings suggest that restoration of Foxo3a function by pharmacological agents under the influence of specific activated protein kinases might constitute a potential therapeutic strategy for combating the CML disease.
众所周知,Foxo3a 是调节红细胞生成的信号转导途径的基本模块;然而,调节其生理功能的确切机制仍不清楚。在这里,我们的结果表明,PKC 和 p38 信号元件的物理相互作用调节 Foxo3a 的核定位和稳定性,并且直接相互作用导致 Foxo3a 中苏氨酸残基的磷酸化。此外,我们的研究结果表明,Foxo3a 通过鸟苷 5'-三磷酸的顺序活性可以抑制 K562 细胞中的细胞增殖并抑制癌蛋白 p73 的表达;从而将 Foxo3a 鉴定为这些 p53 缺失细胞中的肿瘤抑制因子。然而,Foxo3a 依赖性 p73 表达的下调导致沿红细胞谱系的细胞分化。总的来说,我们的研究结果表明,在特定激活蛋白激酶的影响下,通过药理制剂恢复 Foxo3a 功能可能构成对抗 CML 疾病的潜在治疗策略。