Augustyniak J, Lenart J, Zychowicz M, Stepien P P, Buzanska L
Stem Cell Bioengineering Unit, Mossakowski Medical Research Centre Polish Academy of Sciences, Warsaw, Poland.
Department of Neurochemistry, Mossakowski Medical Research Centre Polish Academy of Sciences, Warsaw, Poland.
Biogerontology. 2017 Aug;18(4):665-677. doi: 10.1007/s10522-017-9718-4. Epub 2017 Jun 22.
Idebenone, the synthetic analog of coenzyme Q10 can improve electron transport in mitochondria. Therefore, it is used in the treatment of Alzheimer's disease and other cognitive impairments. However, the mechanism of its action on neurodevelopment is still to be elucidated. Here we demonstrate that the cellular response of human induced pluripotent stem cells (hiPSC) to idebenone depends on the stage of neural differentiation. When: neural stem cells (NSC), early neural progenitors (eNP) and advanced neural progenitors (NP) have been studied a significant stimulation of mitochondrial biogenesis was observed only at the eNP stage of development. This coexists with the enhancement of cell viability and increase in total cell number. In addition, we report novel idebenone properties in a possible regulation of neural stem cells fate decision: only eNP stage responded with up-regulation of both neuronal (MAP2), astrocytic (GFAP) markers, while at NSC and NP stages significant down-regulation of MAP2 expression was observed, promoting astrocyte differentiation. Thus, idebenone targets specific stages of hiPSC differentiation and may influence the neural stem cell fate decision.
艾地苯醌是辅酶Q10的合成类似物,可改善线粒体中的电子传递。因此,它被用于治疗阿尔茨海默病和其他认知障碍。然而,其对神经发育的作用机制仍有待阐明。在此,我们证明人类诱导多能干细胞(hiPSC)对艾地苯醌的细胞反应取决于神经分化阶段。当研究神经干细胞(NSC)、早期神经祖细胞(eNP)和晚期神经祖细胞(NP)时,仅在发育的eNP阶段观察到线粒体生物发生的显著刺激。这与细胞活力的增强和总细胞数的增加同时存在。此外,我们报告了艾地苯醌在可能调节神经干细胞命运决定方面的新特性:只有eNP阶段对神经元(MAP2)和星形胶质细胞(GFAP)标志物的上调有反应,而在NSC和NP阶段观察到MAP2表达显著下调,促进星形胶质细胞分化。因此,艾地苯醌靶向hiPSC分化的特定阶段,并可能影响神经干细胞的命运决定。