Ageing as a two-phase process: theoretical framework

Flaminia Zane, Claire MacMurray, Clémence Guillermain, Céline Cansell, Nicolas Todd, Michael Rera
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Abstract

Human ageing, along with the ageing of conventional model organisms, is depicted as a continuous and progressive decline of biological capabilities accompanied by an exponentially increasing mortality risk. However, not all organisms experience ageing identically and our understanding of the phenomenon is coloured by human-centric views. Ageing is multifaceted and influences a diverse range of species in varying ways. Some undergo swift declines post-reproduction, while others exhibit insubstantial changes throughout their existence. This vast array renders defining universally applicable “ageing attributes” a daunting task. It is nonetheless essential to recognize that not all ageing features are organism-specific. These common attributes have paved the way for identifying “hallmarks of ageing,” processes that are intertwined with age, amplified during accelerated ageing, and manipulations of which can potentially modulate or even reverse the ageing process. Yet, a glaring observation is that individuals within a single population age at varying rates. To address this, demographers have coined the term ‘frailty’. Concurrently, scientific advancements have ushered in the era of molecular clocks. These innovations enable a distinction between an individual’s chronological age (time since birth) and biological age (physiological status and mortality risk). In 2011, the “Smurf” phenotype was unveiled in Drosophila, delineating an age-linked escalation in intestinal permeability that presages imminent mortality. It not only acts as a predictor of natural death but identifies individuals exhibiting traits normally described as age-related. Subsequent studies have revealed the phenotype in organisms like nematodes, zebrafish, and mice, invariably acting as a death predictor. Collectively, these findings have steered our conception of ageing towards a framework where ageing is not linear and continuous but marked by two distinct, necessary phases, discernible in vivo, courtesy of the Smurf phenotype. This framework includes a mathematical enunciation of longevity trends based on three experimentally measurable parameters. It facilitates a fresh perspective on the evolution of ageing as a function. In this article, we aim to delineate and explore the foundational principles of this innovative framework, emphasising its potential to reshape our understanding of ageing, challenge its conventional definitions, and recalibrate our comprehension of its evolutionary trajectory.
老龄化是一个两阶段过程:理论框架
人类的衰老与传统模式生物的衰老一样,被描述为生物能力的持续和逐渐衰退,同时伴随着死亡风险的指数级增长。然而,并非所有生物都会经历相同的衰老,我们对这一现象的理解也受到以人为中心的观点的影响。衰老是多方面的,以不同的方式影响着不同的物种。一些生物在繁殖后迅速衰退,而另一些则在整个生存过程中表现出不明显的变化。由于种类繁多,因此定义普遍适用的 "老化属性 "是一项艰巨的任务。不过,我们必须认识到,并非所有老化特征都是生物特有的。这些共同特征为确定 "老化标志 "铺平了道路,这些标志与年龄交织在一起,在加速老化过程中被放大,对其进行操作有可能调节甚至逆转老化过程。然而,一个明显的现象是,同一人群中的个体衰老速度各不相同。为此,人口学家创造了 "虚弱 "一词。与此同时,科学进步也带来了分子钟时代。这些创新将个人的计时年龄(出生以来的时间)和生物年龄(生理状态和死亡风险)区分开来。2011 年,果蝇的 "蓝精灵 "表型被揭示出来,它描述了与年龄相关的肠道渗透性升级,这种升级预示着即将到来的死亡。它不仅能预测自然死亡,还能识别出表现出通常被描述为与年龄有关的特征的个体。随后的研究揭示了线虫、斑马鱼和小鼠等生物的表型,这些表型无一例外都能预测死亡。总之,这些发现将我们对衰老的概念引向了一个框架,即衰老不是线性的和连续的,而是以两个不同的、必要的阶段为标志的。这一框架包括基于三个实验可测量参数的长寿趋势数学阐述。它有助于以全新的视角看待衰老作为一种功能的演变。在这篇文章中,我们旨在阐述和探讨这一创新框架的基本原则,强调它有可能重塑我们对老龄化的认识,挑战其传统定义,并重新调整我们对其进化轨迹的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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