Conti Bruno, de Cabo Rafael
San Diego Biomedical Research Institute, San Diego, CA, USA.
National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Nat Aging. 2025 May;5(5):740-749. doi: 10.1038/s43587-025-00850-0. Epub 2025 Apr 9.
Core body temperature (T) is a long-established determinant of longevity across species. In this Perspective, we first summarize evidence demonstrating that reducing T increases lifespan and that lowered T contributes to the antiaging effects of calorie restriction. Next, we discuss recent data that diverge from prior hypotheses on the mechanisms by which T affects longevity, suggesting these are limited neither to the thermodynamics of nonenzymatic chemical reactions, nor reduced formation of mitochondrial reactive oxygen species nor lowered metabolic rate. Instead, recent findings in invertebrates show that cold promotes longevity via specific pathways including nutrient sensing and proteostasis, as well as modulating the thermodynamics of proteins and nucleic acids by changing their structure and function, for example, affecting temperature-sensitive ion channels, long-lived temperature-sensitive dauer mutations, base-pair stability and stem-loop RNA structures. Temperature affects the epigenetic signature and inflammation, and lowering T can also induce RNA-binding cold shock proteins, activate cold-sensitive kinases and differential splicing to potentially reshape the cellular environment. Finally, we reflect on important future work and the translational potential of temperature management and temperature mimetics.
核心体温(T)是跨物种长寿的一个长期确定的决定因素。在这篇观点文章中,我们首先总结证据,证明降低体温可延长寿命,且体温降低有助于热量限制的抗衰老作用。接下来,我们讨论最近的数据,这些数据与之前关于体温影响寿命机制的假设不同,表明这些机制既不限于非酶促化学反应的热力学,也不限于线粒体活性氧生成减少或代谢率降低。相反,最近在无脊椎动物中的研究结果表明,寒冷通过特定途径促进长寿,包括营养感知和蛋白质稳态,以及通过改变蛋白质和核酸的结构和功能来调节其热力学,例如,影响温度敏感离子通道、长寿的温度敏感 dauer 突变、碱基对稳定性和茎环 RNA 结构。温度影响表观遗传特征和炎症,降低体温还可诱导 RNA 结合冷休克蛋白,激活冷敏感激酶和差异剪接,从而可能重塑细胞环境。最后,我们思考未来重要的工作以及温度管理和温度模拟物的转化潜力。