Cohen Alan A, Ferrucci Luigi, Fülöp Tamàs, Gravel Dominique, Hao Nan, Kriete Andres, Levine Morgan E, Lipsitz Lewis A, Olde Rikkert Marcel G M, Rutenberg Andrew, Stroustrup Nicholas, Varadhan Ravi
PRIMUS Research Group, Department of Family Medicine, University of Sherbrooke, Sherbrooke, Quebec, Canada.
Research Center on Aging and Research Center of Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, Canada.
Nat Aging. 2022 Jul;2(7):580-591. doi: 10.1038/s43587-022-00252-6. Epub 2022 Jul 20.
Having made substantial progress understanding molecules, cells, genes and pathways, aging biology research is now moving toward integration of these parts, attempting to understand how their joint dynamics may contribute to aging. Such a shift of perspective requires the adoption of a formal complex systems framework, a transition being facilitated by large-scale data collection and new analytical tools. Here, we provide a theoretical framework to orient researchers around key concepts for this transition, notably emergence, interaction networks and resilience. Drawing on evolutionary theory, network theory and principles of homeostasis, we propose that organismal function is accomplished by the integration of regulatory mechanisms at multiple hierarchical scales, and that the disruption of this ensemble causes the phenotypic and functional manifestations of aging. We present key examples at scales ranging from sub-organismal biology to clinical geriatrics, outlining how this approach can potentially enrich our understanding of aging.
在对分子、细胞、基因和信号通路的理解取得了重大进展之后,衰老生物学研究目前正朝着整合这些部分的方向发展,试图了解它们的联合动态如何导致衰老。这种视角的转变需要采用正式的复杂系统框架,大规模数据收集和新的分析工具推动了这一转变。在这里,我们提供了一个理论框架,以帮助研究人员围绕这一转变的关键概念,特别是涌现、相互作用网络和恢复力。借鉴进化理论、网络理论和稳态原理,我们提出,机体功能是通过多个层次尺度的调节机制的整合来实现的,而这种整合的破坏会导致衰老的表型和功能表现。我们展示了从亚生物体生物学到临床老年医学等尺度上的关键例子,概述了这种方法如何有可能丰富我们对衰老的理解。