Mitochondrial biogenesis and neural differentiation of human iPSC is modulated by idebenone in a developmental stage-dependent manner

被引:0
作者
J. Augustyniak
J. Lenart
M. Zychowicz
P. P. Stepien
L. Buzanska
机构
[1] Mossakowski Medical Research Centre Polish Academy of Sciences,Stem Cell Bioengineering Unit
[2] Mossakowski Medical Research Centre Polish Academy of Sciences,Department of Neurochemistry
[3] University of Warsaw,Department of Genetics and Biotechnology, Faculty of Biology
[4] Polish Academy of Sciences,Institute of Biochemistry and Biophysics
[5] University of Warsaw,Centre of New Technologies
来源
Biogerontology | 2017年 / 18卷
关键词
Idebenone; hiPSC; Neural progenitors; Developmental neurotoxicity; Mitochondrial biogenesis; mtDNA copy number; Neuronal; Astrocytic differentiation;
D O I
暂无
中图分类号
学科分类号
摘要
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.
引用
收藏
页码:665 / 677
页数:12
相关论文
empty
未找到相关数据