Carmona Juan José, Michan Shaday
Department of Environmental Health and Program in Quantitative Genomics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Center for Bioethics, Harvard Medical School, Boston, MA, USA.
Rev Invest Clin. 2016 Jan-Feb;68(1):7-16.
As human life expectancy is prolonged, age-related diseases are thriving. Aging is a complex multifactorial process of molecular and cellular decline that affects tissue function over time, rendering organisms frail and susceptible to disease and death. Over the last decades, a growing body of scientific literature across different biological models, ranging from yeast, worms, flies, and mice to primates, humans and other long-lived animals, has contributed greatly towards identifying conserved biological mechanisms that ward off structural and functional deterioration within living systems. Collectively, these data offer powerful insights into healthy aging and longevity. For example, molecular integrity of the genome, telomere length, epigenetic landscape stability, and protein homeostasis are all features linked to "youthful" states. These molecular hallmarks underlie cellular functions associated with aging like mitochondrial fitness, nutrient sensing, efficient intercellular communication, stem cell renewal, and regenerative capacity in tissues. At present, calorie restriction remains the most robust strategy for extending health and lifespan in most biological models tested. Thus, pathways that mediate the beneficial effects of calorie restriction by integrating metabolic signals to aging processes have received major attention, such as insulin/insulin growth factor-1, sirtuins, mammalian target of rapamycin, and 5' adenosine monophosphate-activated protein kinase. Consequently, small-molecule targets of these pathways have emerged in the impetuous search for calorie restriction mimetics, of which resveratrol, metformin, and rapamycin are the most extensively studied. A comprehensive understanding of the molecular and cellular mechanisms that underlie age-related deterioration and repair, and how these pathways interconnect, remains a major challenge for uncovering interventions to slow human aging while extending molecular and physiological youthfulness, vitality, and health. This review summarizes key molecular mechanisms underlying the biology of healthy aging and longevity.
随着人类预期寿命的延长,与年龄相关的疾病日益增多。衰老是一个复杂的多因素分子和细胞衰退过程,随着时间的推移会影响组织功能,使生物体变得虚弱,易患疾病和死亡。在过去几十年里,从酵母、蠕虫、果蝇、小鼠到灵长类动物、人类和其他长寿动物等不同生物模型的科学文献不断增加,这在很大程度上有助于确定保守的生物学机制,以防止生命系统内的结构和功能退化。总体而言,这些数据为健康衰老和长寿提供了有力的见解。例如,基因组的分子完整性、端粒长度、表观遗传景观稳定性和蛋白质稳态都是与“年轻”状态相关的特征。这些分子标志是与衰老相关的细胞功能的基础,如线粒体健康、营养感知、有效的细胞间通讯、干细胞更新和组织再生能力。目前,在大多数测试的生物模型中,热量限制仍然是延长健康和寿命的最有效策略。因此,通过将代谢信号整合到衰老过程中来介导热量限制有益作用的途径受到了主要关注,如胰岛素/胰岛素生长因子-1、沉默调节蛋白、雷帕霉素靶蛋白和5'腺苷单磷酸激活蛋白激酶。因此,在急切寻找热量限制模拟物的过程中,这些途径的小分子靶点出现了,其中白藜芦醇、二甲双胍和雷帕霉素是研究最广泛的。全面了解与年龄相关的衰退和修复背后的分子和细胞机制,以及这些途径如何相互连接,仍然是揭示减缓人类衰老同时延长分子和生理年轻、活力和健康的干预措施的主要挑战。本综述总结了健康衰老和长寿生物学背后的关键分子机制。