Mapuskar Kranti A, London Barry, Zacharias Zeb R, Houtman Jon C D, Allen Bryan G
Department of Radiation Oncology University of Iowa Hospitals and Clinic, University of Iowa Healthcare Iowa City IA USA.
Holden Comprehensive Cancer Center, Carver College of Medicine University of Iowa Hospitals and Clinic, University of Iowa Healthcare Iowa City IA USA.
J Am Heart Assoc. 2025 Jan 7;14(1):e039216. doi: 10.1161/JAHA.124.039216. Epub 2024 Dec 24.
Structural, functional, and molecular-level changes in the aging heart are influenced by a dynamic interplay between immune signaling and cellular metabolism that is referred to as immunometabolism. This review explores the crosstalk between cellular metabolic pathways including glycolysis, oxidative phosphorylation, fatty acid metabolism, and the immune processes that govern cardiac aging. With a rapidly aging population that coincides with increased cardiovascular risk and cancer incidence rates, understanding the immunometabolic underpinnings of cardiac aging provides a foundation for identifying therapeutic targets to mitigate cardiac dysfunction. Aging alters the immune environment of the heart by concomitantly driving the changes in immune cell metabolism, mitochondrial dysfunction, and redox signaling. Shifts in these metabolic pathways exacerbate inflammation and impair tissue repair, creating a vicious cycle that accelerates cardiac functional decline. Treatment with cancer therapy further complicates this landscape, as aging-associated immunometabolic disruptions augment the susceptibility to cardiotoxicity. The current review highlights therapeutic strategies that target the immunometabolic axis to alleviate cardiac aging pathologies. Interventions include modulating metabolic intermediates, improving mitochondrial function, and leveraging immune signaling pathways to restore cardiac health. Advances in immunometabolism thus hold significant potential for translating preclinical findings into therapies that improve the quality of life for the aging population and underscore the need for approaches that address the immunometabolic mechanisms of cardiac aging, providing a framework for future research.
衰老心脏的结构、功能和分子水平变化受到免疫信号与细胞代谢之间动态相互作用的影响,这种相互作用被称为免疫代谢。本综述探讨了细胞代谢途径(包括糖酵解、氧化磷酸化、脂肪酸代谢)与调控心脏衰老的免疫过程之间的相互作用。随着人口迅速老龄化,心血管疾病风险和癌症发病率不断上升,了解心脏衰老的免疫代谢基础为确定减轻心脏功能障碍的治疗靶点提供了基础。衰老通过同时驱动免疫细胞代谢、线粒体功能障碍和氧化还原信号的变化来改变心脏的免疫环境。这些代谢途径的改变会加剧炎症并损害组织修复,从而形成一个加速心脏功能衰退的恶性循环。癌症治疗会使这种情况更加复杂,因为与衰老相关的免疫代谢紊乱会增加心脏毒性的易感性。本综述重点介绍了针对免疫代谢轴以减轻心脏衰老病理的治疗策略。干预措施包括调节代谢中间体、改善线粒体功能以及利用免疫信号通路来恢复心脏健康。因此,免疫代谢方面的进展对于将临床前研究结果转化为改善老年人群生活质量的疗法具有巨大潜力,并强调了需要采用解决心脏衰老免疫代谢机制的方法,为未来研究提供了一个框架。