Su Hetian, Hao Nan
Department of Molecular Biology, School of Biological Sciences, University of California San Diego, La Jolla, California, USA.
Synthetic Biology Institute, University of California San Diego, La Jolla, California, USA.
Quant Biol. 2025 Dec;13(4). doi: 10.1002/qub2.70007. Epub 2025 May 26.
Cellular aging is a multifaceted, complex process. Many genes and factors have been identified that regulate cellular aging. However, how these genes and factors interact with one another and how these interactions drive the aging processes in single cells remain largely unclear. Recently, computational systems biology has demonstrated its potential to empower aging research by providing quantitative descriptions and explanations of complex aging phenotypes, mechanistic insights into the emergent dynamic properties of regulatory networks, and testable predictions that can guide the design of new experiments and interventional strategies. In general, current complex systems approaches can be categorized into two types: (1) network maps that depict the topologies of large-scale molecular networks without detailed characterization of the dynamics of individual components and (2) dynamical models that describe the temporal behavior in a particular set of interacting factors. In this review, we discuss examples that showcase the application of these approaches to cellular aging, with a specific focus on the progress in quantifying and modeling the replicative aging of budding yeast . We further propose potential strategies for integrating network maps and dynamical models toward a more comprehensive, mechanistic, and predictive understanding of cellular aging. Finally, we outline directions and questions in aging research where systems-level approaches may be especially powerful.
细胞衰老 是一个多方面的复杂过程。已经确定了许多调节细胞衰老的基因和因子。然而,这些基因和因子如何相互作用,以及这些相互作用如何驱动单细胞中的衰老过程,在很大程度上仍不清楚。最近,计算系统生物学已显示出其潜力,可通过对复杂衰老表型进行定量描述和解释、对调控网络的新兴动态特性进行机理洞察,以及提供可指导新实验设计和干预策略的可测试预测,来推动衰老研究。一般来说,当前的复杂系统方法可分为两类:(1)描绘大规模分子网络拓扑结构但未详细表征单个组件动态的网络图谱,以及(2)描述特定一组相互作用因子中时间行为的动态模型。在本综述中,我们讨论了展示这些方法在细胞衰老中应用的实例,特别关注在对出芽酵母复制性衰老进行量化和建模方面取得的进展。我们进一步提出了整合网络图谱和动态模型的潜在策略,以更全面、深入和预测性地理解细胞衰老。最后,我们概述了衰老研究中系统水平方法可能特别有效的方向和问题。