Cell reprogramming: Therapeutic potential and the promise of rejuvenation for the aging brain

被引:18
|
作者
Lopez-Leon, Micaela [1 ]
Outeiro, Tiago F. [2 ,3 ]
Goya, Rodolfo G. [1 ]
机构
[1] Natl Univ La Plata, Sch Med, Inst Biochem Res INIBIOLP, Histol B & Pathol B, La Plata, Buenos Aires, Argentina
[2] Univ Med Ctr Gottingen, Ctr Biostruct Imaging Neurodegenerat, Ctr Nanoscale Microscopy & Mol Physiol Brain, Dept Expt Neurodegenerat, Gottingen, Germany
[3] Max Planck Inst Expt Med, Gottingen, Germany
关键词
Brain aging; Cell reprogramming; Rejuvenation; Direct reprogramming; Transdifferentiation; Parkinsons disease; Alzheimer's disease; NEURAL STEM-CELLS; FAMILIAL ALZHEIMERS-DISEASE; ADULT HUMAN FIBROBLASTS; DIRECT CONVERSION; MOUSE FIBROBLASTS; DOPAMINE NEURONS; LINEAGE CONVERSION; FUNCTIONAL-NEURONS; EPIGENETIC REGULATION; PARKINSONS-DISEASE;
D O I
10.1016/j.arr.2017.09.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aging is associated with a progressive increase in the incidence of neurodegenerative diseases, with Alzheimer's (AD) and Parkinson's (PD) disease being the most conspicuous examples. Within this context, the absence of efficacious therapies for most age-related brain pathologies has increased the interest in regenerative medicine. In particular, cell reprogramming technologies have ushered in the era of personalized therapies that not only show a significant potential for the treatment of neurodegenerative diseases but also promise to make biological rejuvenation feasible. We will first review recent evidence supporting the emerging view that aging is a reversible epigenetic phenomenon. Next, we will describe novel reprogramming approaches that overcome some of the intrinsic limitations of conventional induced-pluripotent-stem-cell technology. One of the alternative approaches, lineage reprogramming, consists of the direct conversion of one adult cell type into another by transgenic expression of multiple lineage-specific transcription factors (TF). Another strategy, termed pluripotency factor-mediated direct reprogramming, uses universal TF to generate epigenetically unstable intermediates able to differentiate into somatic cell types in response to specific differentiation factors. In the third part we will review studies showing the potential relevance of the above approaches for the treatment of AD and PD.
引用
收藏
页码:168 / 181
页数:14
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