Abstract & Authors:展开
Aging causes a functional decline in tissues throughout the body that may be delayed by caloric restriction (CR). However, the cellular profiles and signatures of aging, as well as those ameliorated by CR, remain unclear. Here, we built comprehensive single-cell and single-nucleus transcriptomic atlases across various rat tissues undergoing aging and CR. CR attenuated aging-related changes in cell type composition, gene expression, and core transcriptional regulatory networks. Immune cells were increased during aging, and CR favorably reversed the aging-disturbed immune ecosystem. Computational prediction revealed that the abnormal cell-cell communication patterns observed during aging, including the excessive proinflammatory ligand-receptor interplay, were reversed by CR. Our work provides multi-tissue single-cell transcriptional landscapes associated with aging and CR in a mammal, enhances our understanding of the robustness of CR as a geroprotective intervention, and uncovers how metabolic intervention can act upon the immune system to modify the process of aging.
Shuai Ma,Shuhui Sun,Lingling Geng,Moshi Song
Juan Carlos Izpisua Belmonte,Weiqi Zhang,Jing Qu,Guang-Hui Liu
Shuai Ma,Shuhui Sun,Lingling Geng,Moshi Song,Wei Wang,Yanxia Ye,Qianzhao Ji,Zhiran Zou,Si Wang,Xiaojuan He,Wei Li,Concepcion Rodriguez Esteban,Xiao Long,Guoji Guo,Piu Chan,Qi Zhou,Juan Carlos Izpisua Belmonte,Weiqi Zhang,Jing Qu,Guang-Hui Liu