RETRACTED: NF-κB activation impairs somatic cell reprogramming in ageing (Publication with Expression of Concern. See vol. 21, pg. 410, 2019) (Retracted Article)

被引:0
|
作者
Soria-Valles, Clara [1 ]
Osorio, Fernando G. [1 ]
Gutierrez-Fernandez, Ana [1 ]
De Los Angeles, Alejandro [2 ,3 ]
Bueno, Clara [4 ]
Menendez, Pablo [4 ,5 ]
Martin-Subero, Jose I. [6 ]
Daley, George Q. [2 ,3 ,7 ,8 ,9 ]
Freije, Jose M. P. [1 ]
Lopez-Otin, Carlos [1 ]
机构
[1] Univ Oviedo, Fac Med, Inst Univ Oncol, Dept Bioquim & Biol Mol, E-33006 Oviedo, Spain
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston Childrens Hosp, Harvard Stem Cell Inst,Div Hematol Oncol, Boston, MA 02115 USA
[4] Univ Barcelona, Cell Therapy Program, Josep Carreras Leukemia Res Inst, Fac Med, E-08036 Barcelona, Spain
[5] ICREA, Barcelona 08035, Spain
[6] Univ Barcelona, Dept Anat Patol Farmacol & Microbiol, IDIBAPS, E-08036 Barcelona, Spain
[7] Howard Hughes Med Inst, Boston, MA 02115 USA
[8] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[9] Harvard Univ, Sch Med, Cambridge, MA 02138 USA
关键词
PLURIPOTENT STEM-CELLS; SECRETORY PHENOTYPE; PROGERIA SYNDROME; NUCLEAR-ENVELOPE; MICE DEFICIENT; SENESCENCE; METHYLATION; INHIBITION; EXPRESSION; DEFECTS;
D O I
10.1038/ncb3207
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ageing constitutes a critical impediment to somatic cell reprogramming. We have explored the regulatory mechanisms that constitute age-associated barriers, through derivation of induced pluripotent stem cells (iPSCs) from individuals with premature or physiological ageing. We demonstrate that NF-kappa B activation blocks the generation of iPSCs in ageing. We also show that NF-kappa B repression occurs during cell reprogramming towards a pluripotent state. Conversely, ageing-associated NF-kappa B hyperactivation impairs the generation of iPSCs by eliciting the reprogramming repressor DOT1L, which reinforces senescence signals and downregulates pluripotency genes. Genetic and pharmacological NF-kappa B inhibitory strategies significantly increase the reprogramming efficiency of fibroblasts from Nestor-Guillermo progeria syndrome and Hutchinson-Gilford progeria syndrome patients, as well as from normal aged donors. Finally, we demonstrate that DOT1L inhibition in vivo extends lifespan and ameliorates the accelerated ageing phenotype of progeroid mice, supporting the interest of studying age-associated molecular impairments to identify targets of rejuvenation strategies.
引用
收藏
页码:1004 / U320
页数:26
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