Li Qiao, Xiao Nanyin, Zhang Heng, Liang Guangyu, Lin Yan, Qian Zonghao, Yang Xiao, Yang Jiankun, Fu Yanguang, Zhang Cuntai, Liu Anding
Experimental Medicine Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Key Laboratory of Vascular Aging, Ministry of Education, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, P.R. China.
FASEB J. 2025 Mar 15;39(5):e70430. doi: 10.1096/fj.202402479RRR.
Aging is a biological process along with systemic and multiple organ dysfunction. It is more and more recognized that aging is a systemic disease instead of a single-organ functional disorder. Systemic aging plays a profound role in multiple diseases including neurodegenerative diseases, cardiovascular diseases, and malignant diseases. Aged organs communicate with other organs and accelerate aging. Skeletal muscle, heart, bone marrow, skin, and liver communicate with each other through organ-organ crosstalk. The crosstalk can be mediated by metabolites including lipids, glucose, short-chain fatty acids (SCFA), inflammatory cytokines, and exosomes. Metabolic disorders including hyperglycemia, hyperinsulinemia, and hypercholesterolemia caused by chronic diseases accelerate hallmarks of aging. Systemic aging leads to the destruction of systemic hemostasis, causes the release of inflammatory cytokines, senescence-associated secretory phenotype (SASP), and the imbalance of microbiota composition. Released inflammatory factors further aggregate senescence, which promotes the aging of multiple solid organs. Targeting senescence or delaying aging is emerging as a critical health strategy for solving age-related diseases, especially in the old population. In the current review, we will delineate the mechanisms of organ crosstalk in systemic aging and age-related diseases to provide therapeutic targets for delaying aging.
衰老乃是一个伴随全身及多器官功能障碍的生物学过程。人们越来越认识到,衰老并非单一器官功能紊乱,而是一种全身性疾病。全身衰老在包括神经退行性疾病、心血管疾病及恶性疾病在内的多种疾病中起着深远作用。衰老的器官与其他器官相互作用并加速衰老进程。骨骼肌、心脏、骨髓、皮肤和肝脏通过器官间的相互作用进行交流。这种相互作用可由包括脂质、葡萄糖、短链脂肪酸(SCFA)、炎性细胞因子和外泌体在内的代谢产物介导。由慢性病引发的代谢紊乱,如高血糖、高胰岛素血症和高胆固醇血症,会加速衰老的特征。全身衰老会导致全身止血功能遭到破坏,引发炎性细胞因子、衰老相关分泌表型(SASP)的释放以及微生物群组成的失衡。释放出的炎性因子会进一步加剧衰老,从而促进多个实体器官的老化。针对衰老或延缓衰老正成为解决与年龄相关疾病的关键健康策略,尤其是在老年人群体中。在本综述中,我们将阐述全身衰老及与年龄相关疾病中器官相互作用的机制,以为延缓衰老提供治疗靶点。