Leonard Davis School of Gerontology of the Ethel Percy Andrus Gerontology Center, the University of Southern California, Los Angeles, CA, 00089-0191, USA.
Leonard Davis School of Gerontology of the Ethel Percy Andrus Gerontology Center, the University of Southern California, Los Angeles, CA, 00089-0191, USA; Molecular & Computational Biology Program of the Department of Biological Sciences, Dornsife College of Letters, Arts, and sciences, the University of Southern California, Los Angeles, CA, 90089-0191, USA; Department of Biochemistry & Molecular Medicine, Keck School of Medicine of USC, the University of Southern California, Los Angeles, CA, USA.
Mech Ageing Dev. 2019 Jan;177:80-87. doi: 10.1016/j.mad.2018.05.006. Epub 2018 May 17.
Many consequences of ageing can be broadly attributed to the inability to maintain homeostasis. Multiple markers of ageing have been identified, including loss of protein homeostasis, increased inflammation, and declining metabolism. Although much effort has been focused on characterization of the ageing phenotype, much less is understood about the underlying causes of ageing. To address this gap, we outline the age-associated consequences of dysregulation of 'Adaptive Homeostasis' and its proposed contributing role as an accelerator of the ageing phenotype. Adaptive Homeostasis is a phenomenon, shared across cells and tissues of both simple and complex organisms, that enables the transient plastic expansion or contraction of the homeostatic range to modulate stress-protective systems (such as the Proteasome, the Immunoproteasome, and the Lon protease) in response to varying internal and external environments. The age-related rise in the baseline of stress-protective systems and the inability to increase beyond a physiological ceiling is likely a contributor to the reduction and loss of Adaptive Homeostasis. We propose that dysregulation of Adaptive Homeostasis in the final third of lifespan is a significant factor in the ageing process, while successful maintenance of Adaptive Homeostasis below a physiological ceiling results in extended longevity.
许多衰老的后果可以归因于维持体内平衡的能力下降。已经确定了多种衰老标志物,包括蛋白质内稳态丧失、炎症增加和代谢下降。尽管人们已经投入大量精力来描述衰老表型,但对于衰老的根本原因却知之甚少。为了解决这一差距,我们概述了“适应性体内平衡”失调与衰老表型加速之间的关联及其潜在的作用。适应性体内平衡是一种现象,存在于简单和复杂生物体的细胞和组织中,它使稳态范围的短暂可塑性扩张或收缩能够调节应激保护系统(如蛋白酶体、免疫蛋白酶体和 Lon 蛋白酶),以响应不断变化的内部和外部环境。与年龄相关的应激保护系统基线升高,以及无法超过生理上限增加,可能是导致适应性体内平衡减少和丧失的原因之一。我们提出,在生命的最后三分之一时间里,适应性体内平衡失调是衰老过程中的一个重要因素,而在生理上限以下成功维持适应性体内平衡则会导致寿命延长。