Simoroz E V, Vasilevska J, Arakelyan N A, Manakhov A D, Rogaev E I
Research Center for Genetics and Life Sciences, Sirius University of Science and Technology, Sirius Federal Territory, Krasnodar region, Russia.
Research Center for Genetics and Life Sciences, Sirius University of Science and Technology, Sirius Federal Territory, Krasnodar region, Russia Vavilov Institute of General Genetics of the Russian Academy of Sciences, Moscow, Russia.
Vavilovskii Zhurnal Genet Selektsii. 2025 Jul;29(4):496-507. doi: 10.18699/vjgb-25-53.
The progressive shortening of telomeres is significantly implicated in various cellular processes related to aging, including the limitation of cellular proliferative lifespan through the activation of DNA damage response pathways, ultimately leading to replicative senescence. Telomere shortening is considered an indicator of biological age rather than chronological age. The restoration of telomere length is mediated by the enzyme telomerase; however, it is crucial to maintain a balance in this process, as excessive telomerase activity and overly elongated chromosomes may increase the susceptibility of individuals to cancer. It has been proposed that variations in telomere length among individuals of the same chronological age may be associated with differences in potential lifespan. However, recent studies suggest that telomere length may serve only as a rough estimate of the aging process and is likely not a clinically relevant biomarker for age-related diseases or mortality risk. Furthermore, variations in telomere length are not solely determined by chronological age; rather, they are modulated by a multitude of factors, including genetic predispositions, environmental conditions, and heightened metabolic activities such as reproduction and body weight, which may lead to increased telomere attrition in certain species. It has been argued that traditional animal models, such as the mouse (Mus musculus) and the rat (Rattus norvegicus domestica), are suboptimal for investigating the relationship between telomere length and aging, as their lifespans and telomere lengths do not adequately reflect those of humans. Consequently, it is recommended to use long-lived species as they would provide a more appropriate framework for such research initiatives. This review aims to examine the correlation between telomere length and longevity in various non-traditional long-lived animal models, evaluating their suitability for investigating the molecular mechanisms underlying telomere attrition in the context of aging. Nevertheless, the question of whether telomere length is a causative factor or a consequence of longevity remains an area that necessitates further investigation.
端粒的逐渐缩短与衰老相关的各种细胞过程密切相关,包括通过激活DNA损伤反应途径限制细胞增殖寿命,最终导致复制性衰老。端粒缩短被认为是生物年龄而非实际年龄的指标。端粒长度的恢复由端粒酶介导;然而,在这个过程中保持平衡至关重要,因为端粒酶活性过高和染色体过度延长可能会增加个体患癌症的易感性。有人提出,相同实际年龄个体之间端粒长度的差异可能与潜在寿命的差异有关。然而,最近的研究表明,端粒长度可能仅作为衰老过程的粗略估计,可能不是与年龄相关疾病或死亡风险的临床相关生物标志物。此外,端粒长度的变化不仅仅由实际年龄决定;相反,它们受到多种因素的调节,包括遗传易感性、环境条件以及繁殖和体重等增强的代谢活动,这可能导致某些物种的端粒磨损增加。有人认为,传统的动物模型,如小鼠(小家鼠)和大鼠(褐家鼠),对于研究端粒长度与衰老之间的关系并不理想,因为它们的寿命和端粒长度不能充分反映人类的情况。因此,建议使用长寿物种,因为它们将为这类研究提供更合适的框架。本综述旨在研究各种非传统长寿动物模型中端粒长度与长寿之间的相关性,评估它们在衰老背景下研究端粒磨损潜在分子机制的适用性。然而,端粒长度是长寿的致病因素还是结果的问题仍然是一个需要进一步研究的领域。