Induced pluripotent stem cells reprogramming: Epigenetics and applications in the regenerative medicine

被引:8
|
作者
Sampaio Gomes, Katia Maria [1 ]
Costa, Ismael Cabral [1 ]
dos Santos, Jeniffer Farias [2 ]
Martins Dourado, Paulo Magno [3 ]
Forni, Maria Fernanda [4 ]
Batista Ferreira, Julio Cesar [1 ]
机构
[1] Univ Sao Paulo ICB III USP, Inst Biomed Sci III, Dept Anat, Sao Paulo, SP, Brazil
[2] Univ Fed Sao Paulo Unifesp, Dept Biochem, Sao Paulo, SP, Brazil
[3] Univ Sao Paulo InCor FMUSP, Fac Med, Inst Heart, Sao Paulo, SP, Brazil
[4] Univ Sao Paulo IQ USP, Inst Chem, Sao Paulo, SP, Brazil
来源
关键词
induced pluripotent stem cells; regenerative medicine; cell reprogramming; epigenetics; histones; microRNAs; SOMATIC-CELLS; MEDIATED REGULATION; DNA METHYLATION; MICRORNAS; MOUSE; INDUCTION; FIBROBLASTS; PROVIDE; MIR-302; BARRIER;
D O I
10.1590/1806-9282.63.02.180
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Induced pluripotent stem cells ( iPSCs) are somatic cells reprogrammed into an embryonic-like pluripotent state by the expression of specific transcription factors. iPSC technology is expected to revolutionize regenerative medicine in the near future. Despite the fact that these cells have the capacity to self-renew, they present low efficiency of reprogramming. Recent studies have demonstrated that the previous somatic epigenetic signature is a limiting factor in iPSC performance. Indeed, the process of effective reprogramming involves a complete remodeling of the existing somatic epigenetic memory, followed by the establishment of a "new epigenetic signature" that complies with the new type of cell to be differentiated. Therefore, further investigations of epigenetic modifications associated with iPSC reprogramming are required in an attempt to improve their self-renew capacity and potency, as well as their application in regenerative medicine, with a new strategy to reduce the damage in degenerative diseases. Our review aimed to summarize the most recent findings on epigenetics and iPSC, focusing on DNA methylation, histone modifications and microRNAs, highlighting their potential in translating cell therapy into clinics.
引用
收藏
页码:180 / 189
页数:10
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