iPSCs能让时间倒流吗?年龄逆转的前景和缺陷。

IF 2.2
Usama Ahmad, Dinesh Kumar, Md Faiyazuddin
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引用次数: 0

摘要

衰老的特征是细胞功能的逐渐丧失,表观遗传和转录变化的积累,以及组织稳态的下降。诱导多能干细胞(iPSCs),通过表达山中因子(OCT4, SOX2, KLF4, MYC;OSKM),经历表观遗传年轻化,有效地重置了他们的生物年龄。部分重编程以重编程因子的短暂或循环表达为特征,已成为一种很有前途的方法,可以在不消除细胞身份的情况下逆转衰老特征。本研究旨在综合基于ipsc的年龄逆转的研究结果,包括机制、治疗潜力、挑战和转化障碍。虽然部分重编程可以恢复年轻的基因表达、DNA甲基化模式和线粒体功能,并减少衰老标记,但主要的安全性问题仍然存在,包括基因组不稳定、肿瘤发生和对身份保留的不完全控制。该领域正在迅速发展,但在临床转化之前,必须解决有关长期安全性、有效性和最佳方案的基本问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Can iPSCs Turn Back Time? Prospects and Pitfalls in Age Reversal.

Aging is characterized by the progressive loss of cellular function, the accumulation of epigenetic and transcriptional changes, and a decline in tissue homeostasis. Induced pluripotent stem cells (iPSCs), derived from somatic cells through expression of Yamanaka factors (OCT4, SOX2, KLF4, MYC; OSKM), undergo epigenetic rejuvenation, effectively resetting their biological age. Partial reprogramming, characterized by the transient or cyclic expression of reprogramming factors, has emerged as a promising method to reverse aging hallmarks without erasing cellular identity. This study aims to synthesize findings from studies on iPSC-based age reversal, covering mechanisms, therapeutic potential, challenges, and translational hurdles. While partial reprogramming can restore youthful gene expression, DNA methylation patterns, and mitochondrial function, and reduce senescence markers, major safety concerns remain, including genomic instability, tumorigenesis, and incomplete control over identity retention. The field is rapidly progressing, yet fundamental questions about long-term safety, efficacy, and optimal protocols must be resolved before clinical translation.

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