Promoting health and survival through lowered body temperature.

IF 17 Q1 CELL BIOLOGY
Nature aging Pub Date : 2025-05-01 Epub Date: 2025-04-09 DOI:10.1038/s43587-025-00850-0
Bruno Conti, Rafael de Cabo
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引用次数: 0

Abstract

Core body temperature (Tb) is a long-established determinant of longevity across species. In this Perspective, we first summarize evidence demonstrating that reducing Tb increases lifespan and that lowered Tb contributes to the antiaging effects of calorie restriction. Next, we discuss recent data that diverge from prior hypotheses on the mechanisms by which Tb 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 Tb 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.

通过降低体温促进健康和生存。
核心体温(Tb)是物种寿命的一个长期确定的决定因素。在这一观点中,我们首先总结了证明减少结核病可以延长寿命的证据,并且降低结核病有助于卡路里限制的抗衰老作用。接下来,我们讨论了与先前关于结核病影响寿命机制的假设不同的最新数据,表明这些数据既不限于非酶化学反应的热力学,也不限于线粒体活性氧的形成减少或代谢率的降低。相反,最近在无脊椎动物中的发现表明,寒冷通过特定途径促进长寿,包括营养感知和蛋白质静止,以及通过改变蛋白质和核酸的结构和功能来调节蛋白质和核酸的热力学,例如,影响温度敏感的离子通道、长寿命的温度敏感的突变、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Tb还可以诱导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,我们对未来的重要工作和温度管理和温度模拟的转化潜力进行了反思。
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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来源期刊
CiteScore
14.70
自引率
0.00%
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