A high-resolution view of the heterogeneous aging endothelium

被引:4
作者
Dobner, Sarah [1 ]
Toth, Fanni [1 ]
de Rooij, Laura P. M. H. [1 ]
机构
[1] Austrian Acad Sci, CeMM Res Ctr Mol Med, Vienna, Austria
关键词
Endothelial cell heterogeneity; Single-cell RNA-sequencing; Transcriptomics; Vascular aging; CIRCADIAN-RHYTHMS; BLOOD-FLOW; CELL-TYPES; DYSFUNCTION; MECHANISMS; MOUSE; AGE; EXERCISE; ATLAS; VASCULATURE;
D O I
10.1007/s10456-023-09904-6
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Vascular endothelial cell (EC) aging has a strong impact on tissue perfusion and overall cardiovascular health. While studies confined to the investigation of aging-associated vascular readouts in one or a few tissues have already drastically expanded our understanding of EC aging, single-cell omics and other high-resolution profiling technologies have started to illuminate the intricate molecular changes underlying endothelial aging across diverse tissues and vascular beds at scale. In this review, we provide an overview of recent insights into the heterogeneous adaptations of the aging vascular endothelium. We address critical questions regarding tissue-specific and universal responses of the endothelium to the aging process, EC turnover dynamics throughout lifespan, and the differential susceptibility of ECs to acquiring aging-associated traits. In doing so, we underscore the transformative potential of single-cell approaches in advancing our comprehension of endothelial aging, essential to foster the development of future innovative therapeutic strategies for aging-associated vascular conditions.
引用
收藏
页码:129 / 145
页数:17
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