Chen Ying, Tang Liling
Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering Chongqing University, Chongqing 400044, China.
Curr Stem Cell Res Ther. 2019;14(8):654-668. doi: 10.2174/1574888X14666190906163253.
Intervertebral disc (IVD) has a pivotal role in the maintenance of flexible motion. IVD degeneration is one of the primary causes of low back pain and disability, which seriously influences patients' health, and increases the family and social economic burden. Recently, stem cell therapy has been proven to be more effective on IVD degeneration disease. However, stem cell senescence is the limiting factor in the IVD degeneration treatment. Senescent stem cells have a negative effect on the self-repair on IVD degeneration. In this review, we delineate that the factors such as telomerase shortening, DNA damage, oxidative stress, microenvironment and exosomes will induce stem cell aging. Recent studies tried to delay the aging of stem cells by regulating the expression of aging-related genes and proteins, changing the activity of telomerase, improving the survival microenvironment of stem cells and drug treatment. Understanding the mechanism of stem cell aging and exploring new approaches to delay or reverse stem cell aging asks for research on the repair of the degenerated disc.
椎间盘(IVD)在维持灵活运动中起关键作用。椎间盘退变是腰痛和残疾的主要原因之一,严重影响患者健康,增加家庭和社会经济负担。近年来,干细胞疗法已被证明对椎间盘退变疾病更有效。然而,干细胞衰老却是椎间盘退变治疗中的限制因素。衰老的干细胞对椎间盘退变的自我修复有负面影响。在本综述中,我们阐述了端粒酶缩短、DNA损伤、氧化应激、微环境和外泌体等因素会诱导干细胞衰老。最近的研究试图通过调节衰老相关基因和蛋白质的表达、改变端粒酶活性、改善干细胞的生存微环境以及药物治疗来延缓干细胞衰老。了解干细胞衰老的机制并探索延缓或逆转干细胞衰老的新方法需要对退变椎间盘的修复进行研究。