Poisa-Beiro Laura, Landry Jonathan J M, Yan Bowen, Kardorff Michael, Eckstein Volker, Villacorta Laura, Krammer Peter H, Zaugg Judith, Gavin Anne-Claude, Benes Vladimir, Zhou Daohong, Raffel Simon, Ho Anthony D
Department of Medicine V, Heidelberg University, 69117 Heidelberg, Germany.
Molecular Medicine Partnership Unit, European Molecular Biology Laboratories (EMBL) & Heidelberg University, 69117 Heidelberg, Germany.
Int J Mol Sci. 2025 Jan 17;26(2):787. doi: 10.3390/ijms26020787.
To identify the differences between aged and young human hematopoiesis, we performed a direct comparison of aged and young human hematopoietic stem and progenitor cells (HSPCs). Alterations in transcriptome profiles upon aging between humans and mice were then compared. Human specimens consist of CD34+ cells from bone marrow, and mouse specimens of hematopoietic stem cells (HSCs; Lin- Kit+ Sca1+ CD150+). Single-cell transcriptomic studies, functional clustering, and developmental trajectory analyses were performed. A significant increase in multipotent progenitor 2A (MPP2A) cluster is found in the early HSC trajectory in old human subjects. This cluster is enriched in senescence signatures (increased telomere attrition, DNA damage, activation of P53 pathway). In mouse models, the accumulation of an analogous subset was confirmed in the aged LT-HSC population. Elimination of this subset has been shown to rejuvenate hematopoiesis in mice. A significant activation of the P53-P21WAF1/CIP1 pathway was found in the MPP2A population in humans. In contrast, the senescent HSCs in mice are characterized by activation of the p16Ink4a pathway. Aging in the human HSC compartment is mainly caused by the clonal evolution and accumulation of a senescent cell cluster. A population with a similar senescence signature in the aged LT-HSCs was confirmed in the murine aging model. Clearance of this senescent population with senotherapy in humans is feasible and potentially beneficial.
为了确定老年和年轻人类造血功能之间的差异,我们对老年和年轻人类造血干细胞和祖细胞(HSPCs)进行了直接比较。然后比较了人类和小鼠衰老过程中转录组图谱的变化。人类样本由来自骨髓的CD34+细胞组成,小鼠样本为造血干细胞(HSCs;Lin- Kit+ Sca1+ CD150+)。进行了单细胞转录组学研究、功能聚类和发育轨迹分析。在老年人类受试者的早期造血干细胞轨迹中发现多能祖细胞2A(MPP2A)簇显著增加。该簇富含衰老特征(端粒磨损增加、DNA损伤、P53通路激活)。在小鼠模型中,在老年长期造血干细胞群体中证实了类似亚群的积累。已证明消除该亚群可使小鼠造血功能恢复活力。在人类的MPP2A群体中发现了P53-P21WAF1/CIP1通路的显著激活。相比之下,小鼠衰老的造血干细胞的特征是p16Ink4a通路的激活。人类造血干细胞区室的衰老主要是由衰老细胞簇的克隆进化和积累引起的。在小鼠衰老模型中证实了老年长期造血干细胞中有一个具有相似衰老特征的群体。在人类中通过衰老疗法清除这个衰老群体是可行的,而且可能有益。