Replicative and radiation-induced aging: a comparison of gene expression profiles

被引:15
作者
Aliper, Alexander M. [1 ]
Bozdaganyan, Marine E. [1 ]
Orekhov, Philipp S. [1 ,3 ]
Zhavoronkov, Alex [1 ]
Osipov, Andreyan N. [1 ,2 ,3 ]
机构
[1] Inilico Med Inc, Baltimore, MD 21218 USA
[2] FMBC, SRC, Burnasyan Fed Med Biophys Ctr, Moscow 123098, Russia
[3] Moscow Inst Phys & Technol, Dolgoprudnyi, Russia
来源
AGING-US | 2019年 / 11卷 / 08期
基金
俄罗斯科学基金会;
关键词
replicative aging; ionizing radiation; transcriptome analysis; signal pathway transduction; IONIZING-RADIATION; HUMAN FIBROBLASTS; GAMMA-RADIATION; DNA-DAMAGE; ACTIVATION; SENESCENCE; EXPOSURE; SYNDECANS; PATHWAYS; COMPLEX;
D O I
10.18632/aging.101921
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
All living organisms are subject to the aging process and experience the effect of ionizing radiation throughout their life. There have been a number of studies that linked ionizing radiation process to accelerated aging, but comprehensive signalome analysis of both processes was rarely conducted. Here we present a comparative signaling pathway based analysis of the transcriptomes of fibroblasts irradiated with different doses of ionizing radiation, replicatively aged fibroblasts and fibroblasts collected from young, middle age and old patients. We demonstrate a significant concordance between irradiation-induced and replicative senescence signalome signatures of fibroblasts. Additionally, significant differences in transcriptional response were also observed between fibroblasts irradiated with high and low dose. Our data shows that the transcriptome of replicatively aged fibroblasts is more similar to the transcriptome of the cells irradiated with 2 Gy, than with 5 cGy. This work revealed a number of signaling pathways that are shared between senescence and irradiation processes and can potentially be targeted by the new generation of gero-and radioprotectors.
引用
收藏
页码:2378 / 2387
页数:10
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