Cheung Hoi-Hung, Pei Duanqing, Chan Wai-Yee
CUHK-CAS GIBH Joint Research Laboratory on Stem Cell and Regenerative Medicine, School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, Hong Kong S.A.R., China.
Chinese Academy of Sciences (CAS) Guangzhou Institutes of Biomedicine and Health (GIBH), Guangzhou, China.
Cell Regen. 2015 Oct 3;4:6. doi: 10.1186/s13619-015-0021-z. eCollection 2015.
Aging is considered an irreversible biological process and also a major risk factor for a spectrum of geriatric diseases. Advanced age-related decline in physiological functions, such as neurodegeneration, development of cardiovascular disease, endocrine and metabolic dysfunction, and neoplastic transformation, has become the focus in aging research. Natural aging is not regarded as a programmed process. However, accelerated aging due to inherited genetic defects in patients of progeria is programmed and resembles many aspects of natural aging. Among several premature aging syndromes, Werner syndrome (WS) and Hutchinson-Gilford progeria syndrome (HGPS) are two broadly investigated diseases. In this review, we discuss how stem cell aging in WS helps us understand the biology of aging. We also discuss briefly how the altered epigenetic landscape in aged cells can be reversed to a "juvenile" state. Lastly, we explore the potential application of the latest genomic editing technique for stem cell-based therapy and regenerative medicine in the context of aging.
衰老被认为是一个不可逆的生物学过程,也是一系列老年疾病的主要风险因素。与年龄相关的生理功能衰退,如神经退行性变、心血管疾病的发展、内分泌和代谢功能障碍以及肿瘤转化,已成为衰老研究的焦点。自然衰老不被视为一个程序化的过程。然而,早衰患者由于遗传缺陷导致的加速衰老却是程序化的,并且与自然衰老的许多方面相似。在几种早衰综合征中,沃纳综合征(WS)和哈钦森-吉尔福德早衰综合征(HGPS)是两种被广泛研究的疾病。在这篇综述中,我们讨论了WS中的干细胞衰老如何帮助我们理解衰老生物学。我们还简要讨论了衰老细胞中改变的表观遗传格局如何能够被逆转到“年轻”状态。最后,我们探讨了最新基因组编辑技术在衰老背景下基于干细胞的治疗和再生医学中的潜在应用。