Institute for Biochemical Research (INIBIOLP) - Histology B & Pathology B, School of Medicine, National University of La Plata, La Plata, Argentina.
Department of Experimental Neurodegeneration, Center for Nanoscale Microscopy and Molecular Physiology of the Brain, Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Göttingen, Germany; Max Planck Institute for Experimental Medicine, Göttingen, Germany.
Ageing Res Rev. 2017 Nov;40:168-181. doi: 10.1016/j.arr.2017.09.002. Epub 2017 Sep 10.
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.
衰老是神经退行性疾病发病率逐渐增加的一个因素,阿尔茨海默病(AD)和帕金森病(PD)是最明显的例子。在这种情况下,对于大多数与年龄相关的脑部疾病缺乏有效的治疗方法,这增加了对再生医学的兴趣。特别是,细胞重编程技术开创了个性化治疗的时代,不仅对神经退行性疾病的治疗具有显著的潜力,而且有望使生物复兴成为可能。我们将首先回顾最近的证据,支持衰老可逆的表观遗传现象的新兴观点。接下来,我们将描述克服传统诱导多能干细胞技术固有局限性的新型重编程方法。一种替代方法是谱系重编程,通过转导表达多个谱系特异性转录因子(TF)将一种成体细胞类型直接转化为另一种。另一种策略,称为多能因子介导的直接重编程,使用通用 TF 产生表观不稳定的中间产物,这些中间产物能够响应特定的分化因子分化为体细胞类型。在第三部分,我们将回顾显示上述方法对 AD 和 PD 治疗的潜在相关性的研究。