Department of Psychology, University of Washington, Seattle, WA 98195, USA.
Department of Pathology, Nathan Shock Center of Excellence in the Basic Biology of Aging, University of Washington, Seattle, WA 98195, USA.
Philos Trans R Soc Lond B Biol Sci. 2020 Nov 9;375(1811):20190612. doi: 10.1098/rstb.2019.0612. Epub 2020 Sep 21.
Research in the basic biology of ageing is increasingly identifying mechanisms and modifiers of ageing in short-lived organisms such as worms and mice. The ultimate goal of such work is to improve human health, particularly in the growing segment of the population surviving into old age. Thus far, few interventions have robustly transcended species boundaries in the laboratory, suggesting that changes in approach are needed to avoid costly failures in translational human research. In this review, we discuss both well-established and alternative model organisms for ageing research and outline how research in nonhuman primates is sorely needed, first, to translate findings from short-lived organisms to humans, and second, to understand key aspects of ageing that are unique to primate biology. We focus on rhesus macaques as a particularly promising model organism for ageing research owing to their social and physiological similarity to humans as well as the existence of key resources that have been developed for this species. As a case study, we compare gene regulatory signatures of ageing in the peripheral immune system between humans and rhesus macaques from a free-ranging study population in Cayo Santiago. We show that both mRNA expression and DNA methylation signatures of immune ageing are broadly shared between macaques and humans, indicating strong conservation of the trajectory of ageing in the immune system. We conclude with a review of key issues in the biology of ageing for which macaques and other nonhuman primates may uniquely contribute valuable insights, including the effects of social gradients on health and ageing. We anticipate that continuing research in rhesus macaques and other nonhuman primates will play a critical role in conjunction with the model organism and human biodemographic research in ultimately improving translational outcomes and extending health and longevity in our ageing population. This article is part of the theme issue 'Evolution of the primate ageing process'.
衰老的基础生物学研究越来越多地发现了寿命较短的生物体(如蠕虫和老鼠)的衰老机制和调节剂。这项工作的最终目标是改善人类健康,特别是在人口中越来越多的进入老年的人群中。到目前为止,很少有干预措施在实验室中跨越物种界限,这表明需要改变方法,以避免在转化人类研究中代价高昂的失败。在这篇综述中,我们讨论了衰老研究中已经确立的和替代的模式生物,并概述了为什么急需非人类灵长类动物的研究,首先是将从寿命较短的生物体中发现的结果转化到人类身上,其次是了解灵长类生物学所特有的衰老的关键方面。我们专注于恒河猴作为衰老研究的一个特别有前途的模式生物,因为它们在社会和生理上与人类相似,并且存在为这个物种开发的关键资源。作为一个案例研究,我们比较了在圣克洛伊自由放养的研究人群中,人类和恒河猴外周免疫系统衰老的基因调控特征。我们表明,免疫衰老的 mRNA 表达和 DNA 甲基化特征在恒河猴和人类之间广泛共享,这表明免疫系统衰老的轨迹具有很强的保守性。我们以灵长类动物和其他非人类灵长类动物可能独特地为衰老生物学的关键问题提供有价值的见解结束,包括社会梯度对健康和衰老的影响。我们预计,恒河猴和其他非人类灵长类动物的持续研究将与模式生物和人类生物人口学研究一起发挥关键作用,最终改善转化结果,并延长我们老龄化人口的健康和寿命。本文是主题为“灵长类动物衰老过程的进化”的特刊的一部分。